Investigational
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Olumiant (Baricitinib)ExperimentalIf your child is over 2 years old, needs strong and fast relieve, and treatments applied to the skin are not sufficient or appropriateIf you need strong and fast relieve and treatments applied to the skin are not sufficient or appropriateOral once dailyMedium
Side Effect Affected Nasopharyngitis 12% Upper respiratory tract infection 8% Folliculitis 6% Pulmonary embolism 1% Study Summary Study Type Studied Population Results -
Treatment:Olumiant (Baricitinib)ExperimentalEffectiveness:Who is this for?:If you need strong and fast relieve and treatments applied to the skin are not sufficient or appropriateIf your child is over 2 years old, needs strong and fast relieve, and treatments applied to the skin are not sufficient or appropriateSide Effects:Cost:-Delivery:Oral once dailyStudies
Over-the-counter medicine
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Ceramides and Magnesium Cream (Cer-Mg)If you are looking for a moisturizing cream without steroidsIf you are looking for a moisturizing cream without steroidsTopical daily
Side Effect Affected Study Summary Study Type Studied Population Results -
Treatment:Ceramides and Magnesium Cream (Cer-Mg)Effectiveness:Who is this for?:If you are looking for a moisturizing cream without steroidsIf you are looking for a moisturizing cream without steroidsSide Effects:Cost:-Delivery:Topical dailyStudies
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Hydrocortisone (Topical Corticosteroid)For temporary relief of itch and rashesFor temporary relief of itch and rashesTopical daily
Side Effect Affected Study Summary Study Type Studied Population Results -
Treatment:Hydrocortisone (Topical Corticosteroid)Effectiveness:Who is this for?:For temporary relief of itch and rashesFor temporary relief of itch and rashesSide Effects:Cost:-Delivery:Topical 1-4 dailyStudies
Procedure
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Phototherapy (UV-A, Narrowband UV-B)If your child wishes to avoid or reduce reliance on topical and drug treatmentsIf you wish to avoid or reduce reliance on topical and drug treatmentsLight exposure 2-3 times per weekLow
Side Effect Affected Skin redness Skin dryness Study Summary Study Type Studied Population Results -
Treatment:Phototherapy (UV-A, Narrowband UV-B)Effectiveness:Who is this for?:If you wish to avoid or reduce reliance on topical and drug treatmentsIf your child wishes to avoid or reduce reliance on topical and drug treatmentsSide Effects:Cost:-Delivery:Light exposure 2-3 times per weekStudies
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Bleach baths (Sodium hypochlorite)Add-on to other treatments if you experience frequent skin infectionsAdd-on to other treatments if you experience frequent skin infectionsProcedure weekly
Side Effect Affected Study Summary Study Type Studied Population Results -
Treatment:Bleach baths (Sodium hypochlorite)Effectiveness:Who is this for?:Add-on to other treatments if you experience frequent skin infectionsAdd-on to other treatments if you experience frequent skin infectionsSide Effects:Cost:-Delivery:Procedure weeklyStudies
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Allergen-specific immunotherapy (AIT)If your AD is related to allergies and other treatment-options are exhaustedIf your AD is related to allergies and other treatment-options are exhaustedInjection weekly
Side Effect Affected Study Summary Study Type Studied Population Results -
Treatment:Allergen-specific immunotherapy (AIT)Effectiveness:Who is this for?:If your AD is related to allergies and other treatment-options are exhaustedIf your AD is related to allergies and other treatment-options are exhaustedSide Effects:Cost:-Delivery:Injection weeklyStudies
Prescription
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Rinvoq (Upadacitinib)If your child is 12+ years, needs rapid and strong relief of itch and other treatments have failedIf you need rapid and strong relief of itch and other treatments have failedOral once dailyMedium
Side Effect Affected Acne 16% Upper respiratory infections 13% Herpes zoster 5% Elevated liver enzymes 3% Study Summary Study Type Studied Population Results 📄The oral medication upadacitinib showed significant improvement in eczema severity compared to placebo, with higher doses showing better results and an acceptable safety profile.Randomized Controlled Trial 167 adults with moderate-to-severe atopic dermatitis with inadequate control by topical treatmentEASI % improvement: Significant improvement for all doses vs placebo (p=0.03 for 7.5mg, p<0.001 for 15mg and 30mg)
📄Upadacitinib taken once daily as a pill significantly improved eczema symptoms compared to placebo, with 70% of patients on the 15mg dose and 80% on the 30mg dose showing major improvement in their eczema after 16 weeks.Randomized Controlled Trial 847 adolescents (12-17 years) and adults (18-75 years) with moderate-to-severe atopic dermatitisEASI-75: +53.3%
vIGA-AD response: +39.8%
📄Upadacitinib (oral medication) worked better and faster than dupilumab (injection) in treating moderate-to-severe eczema, with 72.4% vs 62.6% of patients achieving significant skin improvement at 16 weeks.Randomized Controlled Trial 673 adults with moderate-to-severe atopic dermatitis📄Upadacitinib (an oral medication) combined with topical steroids was significantly more effective than placebo plus topical steroids in treating moderate-to-severe eczema, with 65-77% of patients showing major improvement compared to 26% on placebo.Randomized Controlled Trial 901 adults (18-75 years) and adolescents (12-17 years) with moderate-to-severe atopic dermatitisEASI-75: +38.1%
vIGA-AD: +28.5%
📄Upadacitinib treatment showed lasting effectiveness through 52 weeks in treating moderate-to-severe atopic dermatitis, with both 15mg and 30mg doses maintaining improvements in skin clearance and itch relief, though the 30mg dose showed slightly better results with some increased side effects.Randomized Controlled Trial 1609 adults and adolescents aged 12-75 years with moderate-to-severe atopic dermatitisEASI-75: 56.0
vIGA-AD 0/1: 48.2
WP-NRS: 52.3
📄Upadacitinib combined with topical steroids was effective and safe for treating moderate-to-severe eczema over a 52-week period, with higher doses showing better improvement in symptoms.Randomized Controlled Trial 901 patients aged 12-75 years with chronic moderate-to-severe atopic dermatitis📄This long-term safety study of upadacitinib across multiple inflammatory conditions showed the medication was generally well-tolerated, with different side effect patterns observed depending on the underlying condition being treated.Observational 6991 patients with rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis and atopic dermatitis📄When comparing different medications, JAK inhibitors were found to have a higher risk of cancer than TNF inhibitors, but showed no difference in cancer risk compared to placebo or methotrexate. Overall, cancer was a rare occurrence across all treatments.Review adults with rheumatoid arthritis, psoriatic arthritis, psoriasis, axial spondyloarthritis, inflammatory bowel disease or atopic dermatitisJAKi vs Placebo IRR: 0.71
JAKi vs Methotrexate IRR: 0.77
JAKi vs TNFi IRR: 1.5
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Treatment:Rinvoq (Upadacitinib)Effectiveness:Who is this for?:If you need rapid and strong relief of itch and other treatments have failedIf your child is 12+ years, needs rapid and strong relief of itch and other treatments have failedSide Effects:Cost:-Delivery:Oral once dailyStudies
Upadacitinib in Adults With Moderate-to-Severe Atopic Dermatitis: 16-Week Results From a Randomized, Placebo-Controlled Trial.
(Full Study)Summary:The oral medication upadacitinib showed significant improvement in eczema severity compared to placebo, with higher doses showing better results and an acceptable safety profile.Study TypeRandomized Controlled TrialStudied Population167 adults with moderate-to-severe atopic dermatitis with inadequate control by topical treatmentResultsEASI % improvement: Significant improvement for all doses vs placebo (p=0.03 for 7.5mg, p<0.001 for 15mg and 30mg)
Once-daily upadacitinib versus placebo in adolescents and adults with moderate-to-severe atopic dermatitis (Measure Up 1 and Measure Up 2): results from two replicate double-blind, randomised controlled phase 3 trials
(Full Study)Summary:Upadacitinib taken once daily as a pill significantly improved eczema symptoms compared to placebo, with 70% of patients on the 15mg dose and 80% on the 30mg dose showing major improvement in their eczema after 16 weeks.Study TypeRandomized Controlled TrialStudied Population847 adolescents (12-17 years) and adults (18-75 years) with moderate-to-severe atopic dermatitisResultsEASI-75: +53.3%
vIGA-AD response: +39.8%
Efficacy and Safety of Upadacitinib vs Dupilumab in Adults With Moderate-to-Severe Atopic Dermatitis
(Full Study)Summary:Upadacitinib (oral medication) worked better and faster than dupilumab (injection) in treating moderate-to-severe eczema, with 72.4% vs 62.6% of patients achieving significant skin improvement at 16 weeks.Study TypeRandomized Controlled TrialStudied Population673 adults with moderate-to-severe atopic dermatitisResults
Safety and efficacy of upadacitinib in combination with topical corticosteroids in adolescents and adults with moderate-to-severe atopic dermatitis (AD Up): results from a randomised, double-blind, placebo-controlled, phase 3 trial
(Full Study)Summary:Upadacitinib (an oral medication) combined with topical steroids was significantly more effective than placebo plus topical steroids in treating moderate-to-severe eczema, with 65-77% of patients showing major improvement compared to 26% on placebo.Study TypeRandomized Controlled TrialStudied Population901 adults (18-75 years) and adolescents (12-17 years) with moderate-to-severe atopic dermatitisResultsEASI-75: +38.1%
vIGA-AD: +28.5%
Efficacy and Safety of Upadacitinib in Patients With Moderate to Severe Atopic Dermatitis
(Full Study)Summary:Upadacitinib treatment showed lasting effectiveness through 52 weeks in treating moderate-to-severe atopic dermatitis, with both 15mg and 30mg doses maintaining improvements in skin clearance and itch relief, though the 30mg dose showed slightly better results with some increased side effects.Study TypeRandomized Controlled TrialStudied Population1609 adults and adolescents aged 12-75 years with moderate-to-severe atopic dermatitisResultsEASI-75: 56.0
vIGA-AD 0/1: 48.2
WP-NRS: 52.3
Upadacitinib plus topical corticosteroids in atopic dermatitis: week-52 AD Up study results.
(Full Study)Summary:Upadacitinib combined with topical steroids was effective and safe for treating moderate-to-severe eczema over a 52-week period, with higher doses showing better improvement in symptoms.Study TypeRandomized Controlled TrialStudied Population901 patients aged 12-75 years with chronic moderate-to-severe atopic dermatitisResults
Safety profile of upadacitinib over 15 000 patient-years across rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis and atopic dermatitis
(Full Study)Summary:This long-term safety study of upadacitinib across multiple inflammatory conditions showed the medication was generally well-tolerated, with different side effect patterns observed depending on the underlying condition being treated.Study TypeObservationalStudied Population6991 patients with rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis and atopic dermatitisResults
JAK inhibitors and the risk of malignancy: a meta-analysis across disease indications
(Full Study)Summary:When comparing different medications, JAK inhibitors were found to have a higher risk of cancer than TNF inhibitors, but showed no difference in cancer risk compared to placebo or methotrexate. Overall, cancer was a rare occurrence across all treatments.Study TypeReviewStudied Populationadults with rheumatoid arthritis, psoriatic arthritis, psoriasis, axial spondyloarthritis, inflammatory bowel disease or atopic dermatitisResultsJAKi vs Placebo IRR: 0.71
JAKi vs Methotrexate IRR: 0.77
JAKi vs TNFi IRR: 1.5
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Cibinqo (Abrocitinib)If your child is 12+ years and needs rapid relief of itch and other symptomsIf you need rapid relief of itch and other symptomsOral once dailyMedium
Side Effect Affected Nausea 15% Headache 8% Acne 5% Decreased platelets 3% Study Summary Study Type Studied Population Results 📄Once-daily oral abrocitinib (200mg or 100mg) significantly improved eczema symptoms compared to placebo in adolescents and adults with moderate-to-severe atopic dermatitis, with improvements seen as early as 2 weeks into treatment.Randomized Controlled Trial 391 patients 12 years or older with moderate-to-severe atopic dermatitisIGA response: 28.7
EASI-75: 50.5
PP-NRS response: 43.8
📄Both doses of oral abrocitinib (100mg and 200mg daily) were more effective than placebo in treating moderate-to-severe eczema, with the 200mg dose showing faster itch relief than dupilumab, though both treatments had similar overall effectiveness at 16 weeks.Randomized Controlled Trial 838 patients with moderate-to-severe atopic dermatitis unresponsive to topical agents or warranting systemic therapy📄The oral medication abrocitinib taken once daily was effective in treating moderate-to-severe eczema in both teens and adults, with higher doses showing better results than lower doses.Randomized Controlled Trial 387 adolescents and adults (≥12 years) with moderate-to-severe atopic dermatitisIGA response: 36% improvement vs placebo
EASI-75: 51% improvement vs placebo
📄Abrocitinib, a daily oral medication, showed manageable safety for long-term use in treating moderate-to-severe eczema, though some side effects like nausea, headache, and infections were observed at different rates depending on the dose.Review 2856 patients with moderate-to-severe atopic dermatitis📄The study found that continuous treatment with abrocitinib helped prevent disease flares in patients who initially responded to treatment, and if flares occurred, restarting treatment was effective in regaining control of symptoms.Randomized Controlled Trial 1233 patients with moderate-to-severe atopic dermatitisResponse regain after flare (IGA 0/1): {'200mg': 36.6, '100mg': 58.8, 'placebo': 81.6}
Response regain after flare (EASI): {'200mg': 55.0, '100mg': 74.5, 'placebo': 91.8}
📄Abrocitinib was effective in treating moderate-to-severe eczema in patients who had previously used dupilumab, regardless of whether they had responded well to dupilumab or not. The medication showed good results in improving both skin symptoms and itch.Observational adults with moderate-to-severe atopic dermatitis who previously received dupilumabEASI-75 dupilumab non-responders 200mg: 80.0
EASI-75 dupilumab non-responders 100mg: 67.7
PP-NRS4 dupilumab non-responders 200mg: 77.3
PP-NRS4 dupilumab non-responders 100mg: 37.8
📄Abrocitinib (oral medication) worked better than dupilumab (injection) at reducing itch and eczema symptoms in adults with moderate-to-severe eczema, particularly in the early weeks of treatment.Randomized Controlled Trial 727 adults with moderate-to-severe atopic dermatitis who required systemic therapy or had inadequate response to topical medicationsPP-NRS4: 22.6% higher in abrocitinib group (p<0.0001)
EASI-90: 14.1% higher in abrocitinib group (p<0.0001)
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Treatment:Cibinqo (Abrocitinib)Effectiveness:Who is this for?:If you need rapid relief of itch and other symptomsIf your child is 12+ years and needs rapid relief of itch and other symptomsSide Effects:Cost:-Delivery:Oral once dailyStudies
Efficacy and Safety of Abrocitinib in Patients With Moderate-to-Severe Atopic Dermatitis
(Full Study)Summary:Once-daily oral abrocitinib (200mg or 100mg) significantly improved eczema symptoms compared to placebo in adolescents and adults with moderate-to-severe atopic dermatitis, with improvements seen as early as 2 weeks into treatment.Study TypeRandomized Controlled TrialStudied Population391 patients 12 years or older with moderate-to-severe atopic dermatitisResultsIGA response: 28.7
EASI-75: 50.5
PP-NRS response: 43.8
Abrocitinib versus Placebo or Dupilumab for Atopic Dermatitis.
(Full Study)Summary:Both doses of oral abrocitinib (100mg and 200mg daily) were more effective than placebo in treating moderate-to-severe eczema, with the 200mg dose showing faster itch relief than dupilumab, though both treatments had similar overall effectiveness at 16 weeks.Study TypeRandomized Controlled TrialStudied Population838 patients with moderate-to-severe atopic dermatitis unresponsive to topical agents or warranting systemic therapyResults
Efficacy and safety of abrocitinib in adults and adolescents with moderate-to-severe atopic dermatitis (JADE MONO-1): a multicentre, double-blind, randomised, placebo-controlled, phase 3 trial
(Full Study)Summary:The oral medication abrocitinib taken once daily was effective in treating moderate-to-severe eczema in both teens and adults, with higher doses showing better results than lower doses.Study TypeRandomized Controlled TrialStudied Population387 adolescents and adults (≥12 years) with moderate-to-severe atopic dermatitisResultsIGA response: 36% improvement vs placebo
EASI-75: 51% improvement vs placebo
Integrated Safety Analysis of Abrocitinib for the Treatment of Moderate-to-Severe Atopic Dermatitis From the Phase II and Phase III Clinical Trial Program
(Full Study)Summary:Abrocitinib, a daily oral medication, showed manageable safety for long-term use in treating moderate-to-severe eczema, though some side effects like nausea, headache, and infections were observed at different rates depending on the dose.Study TypeReviewStudied Population2856 patients with moderate-to-severe atopic dermatitisResults
Abrocitinib induction, randomized withdrawal, and retreatment in patients with moderate to severe atopic dermatitis: results from the JADE REGIMEN phase 3 trial.
(Full Study)Summary:The study found that continuous treatment with abrocitinib helped prevent disease flares in patients who initially responded to treatment, and if flares occurred, restarting treatment was effective in regaining control of symptoms.Study TypeRandomized Controlled TrialStudied Population1233 patients with moderate-to-severe atopic dermatitisResultsResponse regain after flare (IGA 0/1): {'200mg': 36.6, '100mg': 58.8, 'placebo': 81.6}
Response regain after flare (EASI): {'200mg': 55.0, '100mg': 74.5, 'placebo': 91.8}
Phase 3 Efficacy and Safety of Abrocitinib in Adults with Moderate-to-Severe Atopic Dermatitis After Switching from Dupilumab (JADE EXTEND).
(Full Study)Summary:Abrocitinib was effective in treating moderate-to-severe eczema in patients who had previously used dupilumab, regardless of whether they had responded well to dupilumab or not. The medication showed good results in improving both skin symptoms and itch.Study TypeObservationalStudied Populationadults with moderate-to-severe atopic dermatitis who previously received dupilumabResultsEASI-75 dupilumab non-responders 200mg: 80.0
EASI-75 dupilumab non-responders 100mg: 67.7
PP-NRS4 dupilumab non-responders 200mg: 77.3
PP-NRS4 dupilumab non-responders 100mg: 37.8
Efficacy and safety of abrocitinib versus dupilumab in adults with moderate-to-severe atopic dermatitis: a randomised, double-blind, multicentre phase 3 trial
(Full Study)Summary:Abrocitinib (oral medication) worked better than dupilumab (injection) at reducing itch and eczema symptoms in adults with moderate-to-severe eczema, particularly in the early weeks of treatment.Study TypeRandomized Controlled TrialStudied Population727 adults with moderate-to-severe atopic dermatitis who required systemic therapy or had inadequate response to topical medicationsResultsPP-NRS4: 22.6% higher in abrocitinib group (p<0.0001)
EASI-90: 14.1% higher in abrocitinib group (p<0.0001)
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Elidel (Pimecrolimus)If your child needs a long-term, steroid-sparing option and for treatment in sensitive areasIf you need a long-term, steroid-sparing option and for treatment in sensitive areasTopical twice dailyMedium
Side Effect Affected Lymphoma 0.0% Skin burning/irritation 10% Study Summary Study Type Studied Population Results -
Treatment:Elidel (Pimecrolimus)Effectiveness:Who is this for?:If you need a long-term, steroid-sparing option and for treatment in sensitive areasIf your child needs a long-term, steroid-sparing option and for treatment in sensitive areasSide Effects:Cost:-Delivery:Topical twice dailyStudies
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Protopic (Tacrolimus)If your child needs a long-term, steroid-sparing option and for treatment in sensitive areasIf you need a long-term, steroid-sparing option and for treatment in sensitive areasTopical twice daily initially, then twice weekly for maintenanceMedium
Side Effect Affected Burning sensation 45% Lymphoma risk 0.0% Skin infections Study Summary Study Type Studied Population Results 📄These are clinical guidelines for treating eczema (atopic dermatitis) in Japan, recommending the use of topical steroids and tacrolimus ointment as main treatments, along with moisturizers and avoiding triggers.Review patients with atopic dermatitis in Japan📄Atopic dermatitis is a common chronic skin condition affecting 10% of people in their lifetime, with treatment options ranging from basic moisturizers to newer medications like dupilumab, though first-line treatment remains topical corticosteroids.Review general population with atopic dermatitis📄This is a comprehensive position paper that provides guidelines for diagnosing and treating eczema in both adults and children, covering various treatment options from basic moisturizing to advanced medications like dupilumab, and emphasizing the importance of individualized care and education.Review adults and children with atopic dermatitis📄A new way of delivering tacrolimus using tiny carriers called polymeric micelles was more effective at getting the medication into the skin compared to the existing ointment (Protopic), particularly targeting the areas affected by psoriasis without increasing absorption into the bloodstream.Observational human skin samples (ex vivo study)Skin deposition difference: 3.19-fold higher deposition with micelle formulation
📄A case study showed that using tacrolimus eye drops along with other treatments successfully improved severe eye inflammation and skin symptoms in a teenager with atopic dermatitis and eye complications within two months.Observational 1 15-year-old male with atopic keratoconjunctivitis and atopic dermatitisSymptom improvement: Complete resolution of symptoms after 2 months
Quality of life: Significant improvement
📄This paper provides comprehensive guidelines for diagnosing and treating eczema in both adults and children, covering various treatment options from basic moisturizing to advanced medications, and emphasizing the importance of individualized treatment approaches.Review adult and pediatric patients with atopic dermatitis📄Using tacrolimus ointment twice weekly helped prevent vitiligo patches from losing their recovered skin color compared to using a placebo, with only 9.7% of treated areas showing color loss versus 40% in the placebo group.Randomized Controlled Trial 35 adults with successfully repigmented vitiligo patchesdepigmentation_reduction: 21.6% lower depigmentation rate in treatment group
📄This is a European consensus guideline that outlines recommended treatments for eczema, focusing on basic skin care, topical treatments, light therapy, and itch management. The guidelines emphasize that treatment should be personalized since eczema affects everyone differently.Review adults and children with atopic eczema📄People using tacrolimus or pimecrolimus creams for eczema had a slightly higher risk of developing lymphoma compared to those using corticosteroid creams, but the actual number of cases was very small, suggesting minimal risk for individual patients.Observational 988527 children and adults using topical tacrolimus, pimecrolimus, or corticosteroidsLymphoma IRR tacrolimus vs TCS - children: 3.74
Lymphoma IRR tacrolimus vs TCS - adults: 1.27
CTCL IRR tacrolimus vs TCS - adults: 1.76
CTCL IRR pimecrolimus vs TCS - adults: 1.31
CTCL IRR TCS vs untreated - adults: 10.66
📄This expert review provides guidance on which eczema treatments are safe to use during pregnancy planning, pregnancy, and breastfeeding. Topical treatments (like moisturizers, steroid creams) and light therapy are considered safe, while oral medications should be used cautiously and only specific ones are recommended.Review adults with AD who are planning pregnancy, pregnant, or lactating -
Treatment:Protopic (Tacrolimus)Effectiveness:Who is this for?:If you need a long-term, steroid-sparing option and for treatment in sensitive areasIf your child needs a long-term, steroid-sparing option and for treatment in sensitive areasSide Effects:Cost:-Delivery:Topical 0.1% strength for adults, 0.03% for children twice daily initially, then twice weekly for maintenanceStudies
Clinical Practice Guidelines for the Management of Atopic Dermatitis 2016
(Full Study)Summary:These are clinical guidelines for treating eczema (atopic dermatitis) in Japan, recommending the use of topical steroids and tacrolimus ointment as main treatments, along with moisturizers and avoiding triggers.Study TypeReviewStudied Populationpatients with atopic dermatitis in JapanResults
Atopic Dermatitis: Diagnosis and Treatment.
(Full Study)Summary:Atopic dermatitis is a common chronic skin condition affecting 10% of people in their lifetime, with treatment options ranging from basic moisturizers to newer medications like dupilumab, though first-line treatment remains topical corticosteroids.Study TypeReviewStudied Populationgeneral population with atopic dermatitisResults
ETFAD/EADV Eczema task force 2020 position paper on diagnosis and treatment of atopic dermatitis in adults and children
(Full Study)Summary:This is a comprehensive position paper that provides guidelines for diagnosing and treating eczema in both adults and children, covering various treatment options from basic moisturizing to advanced medications like dupilumab, and emphasizing the importance of individualized care and education.Study TypeReviewStudied Populationadults and children with atopic dermatitisResults
Polymeric micelle nanocarriers for the cutaneous delivery of tacrolimus: a targeted approach for the treatment of psoriasis.
(Full Study)Summary:A new way of delivering tacrolimus using tiny carriers called polymeric micelles was more effective at getting the medication into the skin compared to the existing ointment (Protopic), particularly targeting the areas affected by psoriasis without increasing absorption into the bloodstream.Study TypeObservationalStudied Populationhuman skin samples (ex vivo study)ResultsSkin deposition difference: 3.19-fold higher deposition with micelle formulation
Atopic keratoconjunctivitis
(Full Study)Summary:A case study showed that using tacrolimus eye drops along with other treatments successfully improved severe eye inflammation and skin symptoms in a teenager with atopic dermatitis and eye complications within two months.Study TypeObservationalStudied Population1 15-year-old male with atopic keratoconjunctivitis and atopic dermatitisResultsSymptom improvement: Complete resolution of symptoms after 2 months
Quality of life: Significant improvement
ETFAD/EADV Eczema task force 2015 position paper on diagnosis and treatment of atopic dermatitis in adult and paediatric patients
(Full Study)Summary:This paper provides comprehensive guidelines for diagnosing and treating eczema in both adults and children, covering various treatment options from basic moisturizing to advanced medications, and emphasizing the importance of individualized treatment approaches.Study TypeReviewStudied Populationadult and pediatric patients with atopic dermatitisResults
Maintenance therapy of adult vitiligo with 0.1% tacrolimus ointment: a randomized, double blind, placebo-controlled study.
(Full Study)Summary:Using tacrolimus ointment twice weekly helped prevent vitiligo patches from losing their recovered skin color compared to using a placebo, with only 9.7% of treated areas showing color loss versus 40% in the placebo group.Study TypeRandomized Controlled TrialStudied Population35 adults with successfully repigmented vitiligo patchesResultsdepigmentation_reduction: 21.6% lower depigmentation rate in treatment group
Consensus‐based European guidelines for treatment of atopic eczema (atopic dermatitis) in adults and children: part I
(Full Study)Summary:This is a European consensus guideline that outlines recommended treatments for eczema, focusing on basic skin care, topical treatments, light therapy, and itch management. The guidelines emphasize that treatment should be personalized since eczema affects everyone differently.Study TypeReviewStudied Populationadults and children with atopic eczemaResults
A cohort study on the risk of lymphoma and skin cancer in users of topical tacrolimus, pimecrolimus, and corticosteroids (Joint European Longitudinal Lymphoma and Skin Cancer Evaluation – JOELLE study)
(Full Study)Summary:People using tacrolimus or pimecrolimus creams for eczema had a slightly higher risk of developing lymphoma compared to those using corticosteroid creams, but the actual number of cases was very small, suggesting minimal risk for individual patients.Study TypeObservationalStudied Population988527 children and adults using topical tacrolimus, pimecrolimus, or corticosteroidsResultsLymphoma IRR tacrolimus vs TCS - children: 3.74
Lymphoma IRR tacrolimus vs TCS - adults: 1.27
CTCL IRR tacrolimus vs TCS - adults: 1.76
CTCL IRR pimecrolimus vs TCS - adults: 1.31
CTCL IRR TCS vs untreated - adults: 10.66
European task force on atopic dermatitis position paper: treatment of parental atopic dermatitis during preconception, pregnancy and lactation period
(Full Study)Summary:This expert review provides guidance on which eczema treatments are safe to use during pregnancy planning, pregnancy, and breastfeeding. Topical treatments (like moisturizers, steroid creams) and light therapy are considered safe, while oral medications should be used cautiously and only specific ones are recommended.Study TypeReviewStudied Populationadults with AD who are planning pregnancy, pregnant, or lactatingResults
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Dupixent (Dupilumab)If your child is 6+ months and topical treatments don't work for your childIf topical treatments don't work for youInjection every 2 weeksHigh
Side Effect Affected Conjunctivitis 10% Injection site reactions 7% Study Summary Study Type Studied Population Results 📄Adding dupilumab to standard steroid cream treatment for 1 year significantly improved eczema symptoms compared to using steroid cream alone, with acceptable safety.Randomized Controlled Trial 740 adults with moderate-to-severe atopic dermatitis and inadequate response to topical corticosteroidsIGA 0/1: 27% more patients achieved clear/almost clear skin with dupilumab
EASI-75: 46% more patients achieved significant improvement with dupilumab
📄Adding dupilumab injections to nasal steroid spray significantly reduced nasal polyps and improved sense of smell compared to using nasal steroid spray alone in patients with chronic sinusitis.Randomized Controlled Trial 51 adults with chronic sinusitis and nasal polyposis refractory to intranasal corticosteroidsNasal polyp score: -1.6
Lund-Mackay CT score: -8.8
SinoNasal Outcome Test: -18.1
UPSIT score: 14.8
📄Dupilumab significantly improved eczema symptoms compared to placebo, with the strongest improvements seen in higher doses given more frequently. The treatment was generally safe with similar side effects between treatment and placebo groups.Randomized Controlled Trial 379 adults with moderate-to-severe atopic dermatitis inadequately controlled by topical treatmentsEASI % change: 50% greater improvement with dupilumab compared to placebo
📄Dupilumab treatment improved eczema symptoms and skin health at the cellular level, while being well-tolerated by patients. The drug worked by reducing inflammation and improving skin barrier function over a 16-week period.Randomized Controlled Trial 54 patients with moderate-to-severe atopic dermatitisTranscriptome improvement: Significant improvement vs placebo (p<0.001)
Epidermal thickness: Significant reduction vs placebo (week 4: p=0.001, week 16: p=0.0002)
📄Dupilumab treatment improved the molecular markers of atopic dermatitis in skin samples, showing that it effectively targets and reduces inflammation associated with the condition.Randomized Controlled Trial patients with moderate-to-severe atopic dermatitisGene expression improvement: Dose-dependent improvement with greater effects at 300mg dose
TH2-associated chemokines: Significant decrease
Hyperplasia markers: Significant decrease
📄Dupilumab with topical steroids significantly improved eczema symptoms in adults who couldn't use or didn't respond to ciclosporin A, with about 60% of patients showing major improvement compared to 30% on placebo.Randomized Controlled Trial 318 adults with atopic dermatitis with inadequate response to/intolerance of ciclosporin A, or for whom ciclosporin A treatment was medically inadvisableEASI-75: 33% improvement over placebo
📄Patients taking dupilumab for atopic dermatitis had a higher chance of developing eye inflammation (conjunctivitis) compared to placebo, particularly if they had severe AD or previous eye problems, but this side effect was rare in patients taking the drug for other conditions.Review 5612 patients with atopic dermatitis, asthma, chronic rhinosinusitis with nasal polyps, and eosinophilic oesophagitis📄Dupilumab significantly improved eczema symptoms, itching, and quality of life in adolescents with moderate-to-severe atopic dermatitis compared to placebo, with an acceptable safety profile.Randomized Controlled Trial 251 adolescents aged 12-17 years with moderate-to-severe atopic dermatitis inadequately controlled by topical medicationsEASI-75: 33.2
IGA 0/1: 22.0
Peak Pruritus NRS: -29.0
📄Dupilumab significantly improved eczema symptoms, itching, anxiety, depression, and quality of life compared to placebo in adults with moderate-to-severe eczema over 16 weeks of treatment.Randomized Controlled Trial 1379 adults with moderate-to-severe atopic dermatitis inadequately controlled by topical treatmentIGA 0/1: 28% more patients achieved clear/almost clear skin with dupilumab vs placebo
EASI-75: 28% more patients achieved 75% improvement with dupilumab vs placebo
📄Dupilumab treatment showed rapid and significant improvement in eczema symptoms compared to placebo, with most patients showing at least 50% improvement in their condition. The medication was well-tolerated with mainly mild side effects like nasopharyngitis and headache.Randomized Controlled Trial adults with moderate-to-severe atopic dermatitisEASI-50: 50 percentage point improvement over placebo
IGA 0-1: 33 percentage point improvement over placebo
Pruritus: 40.6 percentage point improvement over placebo
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Treatment:Dupixent (Dupilumab)Effectiveness:Who is this for?:If topical treatments don't work for youIf your child is 6+ months and topical treatments don't work for your childSide Effects:Cost:-Delivery:Injection None every 2 weeksStudies
Long-term management of moderate-to-severe atopic dermatitis with dupilumab and concomitant topical corticosteroids (LIBERTY AD CHRONOS): a 1-year, randomised, double-blinded, placebo-controlled, phase 3 trial
(Full Study)Summary:Adding dupilumab to standard steroid cream treatment for 1 year significantly improved eczema symptoms compared to using steroid cream alone, with acceptable safety.Study TypeRandomized Controlled TrialStudied Population740 adults with moderate-to-severe atopic dermatitis and inadequate response to topical corticosteroidsResultsIGA 0/1: 27% more patients achieved clear/almost clear skin with dupilumab
EASI-75: 46% more patients achieved significant improvement with dupilumab
Effect of Subcutaneous Dupilumab on Nasal Polyp Burden in Patients With Chronic Sinusitis and Nasal Polyposis: A Randomized Clinical Trial.
(Full Study)Summary:Adding dupilumab injections to nasal steroid spray significantly reduced nasal polyps and improved sense of smell compared to using nasal steroid spray alone in patients with chronic sinusitis.Study TypeRandomized Controlled TrialStudied Population51 adults with chronic sinusitis and nasal polyposis refractory to intranasal corticosteroidsResultsNasal polyp score: -1.6
Lund-Mackay CT score: -8.8
SinoNasal Outcome Test: -18.1
UPSIT score: 14.8
Efficacy and safety of dupilumab in adults with moderate-to-severe atopic dermatitis inadequately controlled by topical treatments: a randomised, placebo-controlled, dose-ranging phase 2b trial
(Full Study)Summary:Dupilumab significantly improved eczema symptoms compared to placebo, with the strongest improvements seen in higher doses given more frequently. The treatment was generally safe with similar side effects between treatment and placebo groups.Study TypeRandomized Controlled TrialStudied Population379 adults with moderate-to-severe atopic dermatitis inadequately controlled by topical treatmentsResultsEASI % change: 50% greater improvement with dupilumab compared to placebo
Dupilumab progressively improves systemic and cutaneous abnormalities in patients with atopic dermatitis
(Full Study)Summary:Dupilumab treatment improved eczema symptoms and skin health at the cellular level, while being well-tolerated by patients. The drug worked by reducing inflammation and improving skin barrier function over a 16-week period.Study TypeRandomized Controlled TrialStudied Population54 patients with moderate-to-severe atopic dermatitisResultsTranscriptome improvement: Significant improvement vs placebo (p<0.001)
Epidermal thickness: Significant reduction vs placebo (week 4: p=0.001, week 16: p=0.0002)
Dupilumab improves the molecular signature in skin of patients with moderate-to-severe atopic dermatitis.
(Full Study)Summary:Dupilumab treatment improved the molecular markers of atopic dermatitis in skin samples, showing that it effectively targets and reduces inflammation associated with the condition.Study TypeRandomized Controlled TrialStudied Populationpatients with moderate-to-severe atopic dermatitisResultsGene expression improvement: Dose-dependent improvement with greater effects at 300mg dose
TH2-associated chemokines: Significant decrease
Hyperplasia markers: Significant decrease
Dupilumab with concomitant topical corticosteroid treatment in adults with atopic dermatitis with an inadequate response or intolerance to ciclosporin A or when this treatment is medically inadvisable: a placebo‐controlled, randomized phase III clinical trial (LIBERTY AD CAFÉ)
(Full Study)Summary:Dupilumab with topical steroids significantly improved eczema symptoms in adults who couldn't use or didn't respond to ciclosporin A, with about 60% of patients showing major improvement compared to 30% on placebo.Study TypeRandomized Controlled TrialStudied Population318 adults with atopic dermatitis with inadequate response to/intolerance of ciclosporin A, or for whom ciclosporin A treatment was medically inadvisableResultsEASI-75: 33% improvement over placebo
Conjunctivitis in dupilumab clinical trials
(Full Study)Summary:Patients taking dupilumab for atopic dermatitis had a higher chance of developing eye inflammation (conjunctivitis) compared to placebo, particularly if they had severe AD or previous eye problems, but this side effect was rare in patients taking the drug for other conditions.Study TypeReviewStudied Population5612 patients with atopic dermatitis, asthma, chronic rhinosinusitis with nasal polyps, and eosinophilic oesophagitisResults
Efficacy and Safety of Dupilumab in Adolescents With Uncontrolled Moderate to Severe Atopic Dermatitis
(Full Study)Summary:Dupilumab significantly improved eczema symptoms, itching, and quality of life in adolescents with moderate-to-severe atopic dermatitis compared to placebo, with an acceptable safety profile.Study TypeRandomized Controlled TrialStudied Population251 adolescents aged 12-17 years with moderate-to-severe atopic dermatitis inadequately controlled by topical medicationsResultsEASI-75: 33.2
IGA 0/1: 22.0
Peak Pruritus NRS: -29.0
Two Phase 3 Trials of Dupilumab versus Placebo in Atopic Dermatitis.
(Full Study)Summary:Dupilumab significantly improved eczema symptoms, itching, anxiety, depression, and quality of life compared to placebo in adults with moderate-to-severe eczema over 16 weeks of treatment.Study TypeRandomized Controlled TrialStudied Population1379 adults with moderate-to-severe atopic dermatitis inadequately controlled by topical treatmentResultsIGA 0/1: 28% more patients achieved clear/almost clear skin with dupilumab vs placebo
EASI-75: 28% more patients achieved 75% improvement with dupilumab vs placebo
Dupilumab treatment in adults with moderate-to-severe atopic dermatitis.
(Full Study)Summary:Dupilumab treatment showed rapid and significant improvement in eczema symptoms compared to placebo, with most patients showing at least 50% improvement in their condition. The medication was well-tolerated with mainly mild side effects like nasopharyngitis and headache.Study TypeRandomized Controlled TrialStudied Populationadults with moderate-to-severe atopic dermatitisResultsEASI-50: 50 percentage point improvement over placebo
IGA 0-1: 33 percentage point improvement over placebo
Pruritus: 40.6 percentage point improvement over placebo
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Opzelura (Ruxolitinib)If your child is 12+ years and looking for a short-term treatment with rapid relief of itch and inflammation, and other topical treatments have failedIf you are looking for a short-term treatment with rapid relief of itch and inflammation, and other topical treatments have failedTopical twice dailyHigh
Side Effect Affected Nasopharyngitis 3% Application site reactions 1% Study Summary Study Type Studied Population Results -
Treatment:Opzelura (Ruxolitinib)Effectiveness:Who is this for?:If you are looking for a short-term treatment with rapid relief of itch and inflammation, and other topical treatments have failedIf your child is 12+ years and looking for a short-term treatment with rapid relief of itch and inflammation, and other topical treatments have failedSide Effects:Cost:-Delivery:Topical thin film to affected areas twice dailyStudies
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Adbry (Tralokinumab)If you are 12+ years and topical prescription therapies don't work for youIf topical prescription therapies don't work for youInjection every 2 weeksHigh
Side Effect Affected Viral upper respiratory tract infection 16% Conjunctivitis 5% Injection site reactions 4% Study Summary Study Type Studied Population Results -
Treatment:Adbry (Tralokinumab)Effectiveness:Who is this for?:If topical prescription therapies don't work for youIf you are 12+ years and topical prescription therapies don't work for youSide Effects:Cost:-Delivery:Injection 300mg every 2 weeksStudies
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Ebglyss (Lebrikizumab)If you are 12+, need strong relief and topical treatments don't work for youIf you need strong relief and topical treatments don't work for youInjection every 2-4 weeksHigh
Side Effect Affected Upper respiratory tract infection 5% Injection site reactions 6% Conjunctivitis 3% Study Summary Study Type Studied Population Results 📄When combined with topical steroids, lebrikizumab taken every 4 weeks significantly improved eczema symptoms compared to placebo, with similar side effects between groups.Randomized Controlled Trial 209 adults with moderate-to-severe atopic dermatitis inadequately controlled by topical corticosteroidsEASI-50: 20.1% improvement over placebo (p = 0.026)
📄IL-13 plays a key role in atopic dermatitis, and drugs that block IL-13 (like tralokinumab and lebrikizumab) show promising results in treating moderate-to-severe eczema.Review patients with moderate-to-severe atopic dermatitis📄Lebrikizumab, given as an injection every 2 weeks, was significantly more effective than placebo in clearing skin and reducing itch in people with moderate-to-severe eczema over 16 weeks of treatment.Randomized Controlled Trial 851 adults (≥18 years) and adolescents (12-17 years, ≥40 kg) with moderate-to-severe atopic dermatitisIGA 0/1: 30.4% improvement over placebo in trial 1, 22.4% in trial 2
EASI-75: 42.6% improvement over placebo in trial 1, 34% in trial 2
📄Lebrikizumab showed significant improvement in eczema symptoms compared to placebo over 16 weeks, with benefits seen as early as day 2 for itch relief. The medication was generally well-tolerated with few side effects.Randomized Controlled Trial 280 adults with moderate-to-severe atopic dermatitis📄Lebrikizumab was effective at treating moderate-to-severe eczema over 52 weeks, with similar results whether given every 2 or 4 weeks after the initial 16-week treatment period. The medication was generally safe with most side effects being mild or moderate.Randomized Controlled Trial adolescent and adult patients with moderate-to-severe atopic dermatitis📄This review discusses new treatments for eczema in children, including recently FDA-approved medications (crisaborole and dupilumab) and promising emerging therapies that target specific pathways in the immune system, potentially offering better effectiveness with fewer side effects than traditional treatments.Review pediatric patients with atopic dermatitis📄This laboratory study showed that IL-13 affects genes associated with skin barrier function and inflammation in atopic dermatitis, and that tralokinumab can block these effects.Observational human skin cells in laboratory📄Several new biologic medications (lebrikizumab, tralokinumab, fezakinumab, nemolizumab, and GBR 830) showed promising results in treating moderate-to-severe atopic dermatitis in adults, while two others (tezepelumab and etokimab) did not show significant improvements.Review adults with moderate-to-severe AD📄Using computer analysis of genetic data, researchers identified 53 existing drugs that might be useful for treating atopic dermatitis, including some that are already being tested or used for this condition.Review genomic data analysis -
Treatment:Ebglyss (Lebrikizumab)Effectiveness:Who is this for?:If you need strong relief and topical treatments don't work for youIf you are 12+, need strong relief and topical treatments don't work for youSide Effects:Cost:-Delivery:Injection every 2-4 weeksStudies
Efficacy and safety of lebrikizumab (an anti‐IL‐13 monoclonal antibody) in adults with moderate‐to‐severe atopic dermatitis inadequately controlled by topical corticosteroids: A randomized, placebo‐controlled phase II trial (TREBLE)
(Full Study)Summary:When combined with topical steroids, lebrikizumab taken every 4 weeks significantly improved eczema symptoms compared to placebo, with similar side effects between groups.Study TypeRandomized Controlled TrialStudied Population209 adults with moderate-to-severe atopic dermatitis inadequately controlled by topical corticosteroidsResultsEASI-50: 20.1% improvement over placebo (p = 0.026)
Therapeutic targeting of the IL-13 pathway in skin inflammation
(Full Study)Summary:IL-13 plays a key role in atopic dermatitis, and drugs that block IL-13 (like tralokinumab and lebrikizumab) show promising results in treating moderate-to-severe eczema.Study TypeReviewStudied Populationpatients with moderate-to-severe atopic dermatitisResults
Two Phase 3 Trials of Lebrikizumab for Moderate-to-Severe Atopic Dermatitis.
(Full Study)Summary:Lebrikizumab, given as an injection every 2 weeks, was significantly more effective than placebo in clearing skin and reducing itch in people with moderate-to-severe eczema over 16 weeks of treatment.Study TypeRandomized Controlled TrialStudied Population851 adults (≥18 years) and adolescents (12-17 years, ≥40 kg) with moderate-to-severe atopic dermatitisResultsIGA 0/1: 30.4% improvement over placebo in trial 1, 22.4% in trial 2
EASI-75: 42.6% improvement over placebo in trial 1, 34% in trial 2
Efficacy and Safety of Lebrikizumab, a High-Affinity Interleukin 13 Inhibitor, in Adults With Moderate to Severe Atopic Dermatitis
(Full Study)Summary:Lebrikizumab showed significant improvement in eczema symptoms compared to placebo over 16 weeks, with benefits seen as early as day 2 for itch relief. The medication was generally well-tolerated with few side effects.Study TypeRandomized Controlled TrialStudied Population280 adults with moderate-to-severe atopic dermatitisResults
Efficacy and safety of lebrikizumab in moderate-to-severe atopic dermatitis: 52-week results of two randomized double-blinded placebo-controlled phase III trials.
(Full Study)Summary:Lebrikizumab was effective at treating moderate-to-severe eczema over 52 weeks, with similar results whether given every 2 or 4 weeks after the initial 16-week treatment period. The medication was generally safe with most side effects being mild or moderate.Study TypeRandomized Controlled TrialStudied Populationadolescent and adult patients with moderate-to-severe atopic dermatitisResults
New and Emerging Therapies for Pediatric Atopic Dermatitis
(Full Study)Summary:This review discusses new treatments for eczema in children, including recently FDA-approved medications (crisaborole and dupilumab) and promising emerging therapies that target specific pathways in the immune system, potentially offering better effectiveness with fewer side effects than traditional treatments.Study TypeReviewStudied Populationpediatric patients with atopic dermatitisResults
Skin Barrier and Inflammation Genes Associated with Atopic Dermatitis are Regulated by Interleukin-13 and Modulated by Tralokinumab In vitro
(Full Study)Summary:This laboratory study showed that IL-13 affects genes associated with skin barrier function and inflammation in atopic dermatitis, and that tralokinumab can block these effects.Study TypeObservationalStudied Populationhuman skin cells in laboratoryResults
Review and analysis of biologic therapies currently in phase II and phase III clinical trials for atopic dermatitis
(Full Study)Summary:Several new biologic medications (lebrikizumab, tralokinumab, fezakinumab, nemolizumab, and GBR 830) showed promising results in treating moderate-to-severe atopic dermatitis in adults, while two others (tezepelumab and etokimab) did not show significant improvements.Study TypeReviewStudied Populationadults with moderate-to-severe ADResults
Drug Repurposing for Atopic Dermatitis by Integration of Gene Networking and Genomic Information
(Full Study)Summary:Using computer analysis of genetic data, researchers identified 53 existing drugs that might be useful for treating atopic dermatitis, including some that are already being tested or used for this condition.Study TypeReviewStudied Populationgenomic data analysisResults
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Eucrisa (Crisaborole)If your child needs a non-steroid topical treatment, especially in sensitive areasIf you need a non-steroid topical treatment, especially in sensitive areasTopical twice dailyHigh
Side Effect Affected Application site pain 4% Application site discomfort 3% Erythema 3% Study Summary Study Type Studied Population Results 📄Crisaborole ointment was more effective than placebo at treating eczema symptoms and was found to be safe with mostly mild side effects when applied twice daily for 28 days.Randomized Controlled Trial children and adults with mild to moderate atopic dermatitisISGA success: Significantly higher success rates in crisaborole group (p=0.038 in AD-301, p<0.001 in AD-302)
Time to improvement: Crisaborole achieved success faster than vehicle (p≤0.001)
📄Crisaborole 2% ointment applied twice daily showed limited absorption into the body and was generally safe when used by teenagers with eczema, with some patients showing improvement in their condition after 29 days.Observational 23 adolescents aged 12-17 years with mild to moderate atopic dermatitis affecting 10-35% body surface areaBSA reduction: Decreased from 17.6% to 8.2%
📄Crisaborole ointment 2% was found to be safe and effective when used twice daily in infants with mild-to-moderate eczema, with most side effects being mild and occurring at the application site.Observational 137 infants aged 3 to < 24 months with mild-to-moderate atopic dermatitisISGA clear/almost clear: 30.2% achieved clear/almost clear with ≥2-grade improvement
EASI score: 57.5% improvement
POEM score: 8.5 point reduction
📄Crisaborole 2% ointment was more effective than placebo in treating eczema lesions, with 68% of patients showing better improvement in the treated area compared to the untreated area. The medication was generally safe with mostly mild side effects.Randomized Controlled Trial 25 adults with mild to moderate atopic dermatitisADSI improvement: 68% of patients had greater improvement in treated lesion vs vehicle-treated lesion
📄Crisaborole ointment applied twice daily at 2% strength was effective in treating mild to moderate eczema in teenagers, improving symptoms by 71% after 29 days with only mild side effects at the application site.Randomized Controlled Trial 86 adolescents 12-17 years with mild to moderate atopic dermatitis📄Topical PDE4 inhibitors (particularly crisaborole and AN2898) were found to be safe and effective treatments for mild to moderate eczema, showing significant improvement in skin symptoms compared to vehicle (placebo) treatment.Review 1869 patients with mild to moderate atopic dermatitisTarget lesion score: SMD -0.40 (95% CI, -0.61 to -0.18, P < .001)
Clear/almost clear skin: 50% higher response rate compared to control (RR 1.50; 95% CI, 1.33-1.70; P < .001)
📄Atopic dermatitis is a common chronic skin condition affecting 10% of people in their lifetime, characterized by itchy skin lesions. Treatment typically includes moisturizers, gentle cleansers, and topical corticosteroids as first-line therapy, with newer treatments available for more severe cases.Review general population with atopic dermatitis📄Crisaborole ointment showed good safety when used for up to 48 weeks, with most side effects being mild and not related to the treatment.Observational 517 children and adults (≥2 years) with mild to moderate atopic dermatitis📄Crisaborole 2% ointment applied twice daily was found to be safe with limited absorption into the body, and helped improve eczema symptoms in children aged 2-17 years when applied for 28 days.Observational 34 children ages 2-17 years with mild to moderate AD involving 25% or more treatable body surface areaISGA change from baseline: -1.5
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Treatment:Eucrisa (Crisaborole)Effectiveness:Who is this for?:If you need a non-steroid topical treatment, especially in sensitive areasIf your child needs a non-steroid topical treatment, especially in sensitive areasSide Effects:Cost:-Delivery:Topical twice dailyStudies
Efficacy and safety of crisaborole ointment, a novel, nonsteroidal phosphodiesterase 4 (PDE4) inhibitor for the topical treatment of atopic dermatitis (AD) in children and adults.
(Full Study)Summary:Crisaborole ointment was more effective than placebo at treating eczema symptoms and was found to be safe with mostly mild side effects when applied twice daily for 28 days.Study TypeRandomized Controlled TrialStudied Populationchildren and adults with mild to moderate atopic dermatitisResultsISGA success: Significantly higher success rates in crisaborole group (p=0.038 in AD-301, p<0.001 in AD-302)
Time to improvement: Crisaborole achieved success faster than vehicle (p≤0.001)
Pharmacokinetic Profile, Safety, and Tolerability of Crisaborole Topical Ointment, 2% in Adolescents with Atopic Dermatitis: An Open‐Label Phase 2a Study
(Full Study)Summary:Crisaborole 2% ointment applied twice daily showed limited absorption into the body and was generally safe when used by teenagers with eczema, with some patients showing improvement in their condition after 29 days.Study TypeObservationalStudied Population23 adolescents aged 12-17 years with mild to moderate atopic dermatitis affecting 10-35% body surface areaResultsBSA reduction: Decreased from 17.6% to 8.2%
Safety, Effectiveness, and Pharmacokinetics of Crisaborole in Infants Aged 3 to < 24 Months with Mild-to-Moderate Atopic Dermatitis: A Phase IV Open-Label Study (CrisADe CARE 1)
(Full Study)Summary:Crisaborole ointment 2% was found to be safe and effective when used twice daily in infants with mild-to-moderate eczema, with most side effects being mild and occurring at the application site.Study TypeObservationalStudied Population137 infants aged 3 to < 24 months with mild-to-moderate atopic dermatitisResultsISGA clear/almost clear: 30.2% achieved clear/almost clear with ≥2-grade improvement
EASI score: 57.5% improvement
POEM score: 8.5 point reduction
Crisaborole Topical Ointment, 2% in Adults With Atopic Dermatitis: A Phase 2a, Vehicle-Controlled, Proof-of-Concept Study.
(Full Study)Summary:Crisaborole 2% ointment was more effective than placebo in treating eczema lesions, with 68% of patients showing better improvement in the treated area compared to the untreated area. The medication was generally safe with mostly mild side effects.Study TypeRandomized Controlled TrialStudied Population25 adults with mild to moderate atopic dermatitisResultsADSI improvement: 68% of patients had greater improvement in treated lesion vs vehicle-treated lesion
A Phase 2, Randomized, Controlled, Dose-Ranging Study Evaluating Crisaborole Topical Ointment, 0.5% and 2% in Adolescents With Mild to Moderate Atopic Dermatitis.
(Full Study)Summary:Crisaborole ointment applied twice daily at 2% strength was effective in treating mild to moderate eczema in teenagers, improving symptoms by 71% after 29 days with only mild side effects at the application site.Study TypeRandomized Controlled TrialStudied Population86 adolescents 12-17 years with mild to moderate atopic dermatitisResults
Application of Topical Phosphodiesterase 4 Inhibitors in Mild to Moderate Atopic Dermatitis: A Systematic Review and Meta-analysis
(Full Study)Summary:Topical PDE4 inhibitors (particularly crisaborole and AN2898) were found to be safe and effective treatments for mild to moderate eczema, showing significant improvement in skin symptoms compared to vehicle (placebo) treatment.Study TypeReviewStudied Population1869 patients with mild to moderate atopic dermatitisResultsTarget lesion score: SMD -0.40 (95% CI, -0.61 to -0.18, P < .001)
Clear/almost clear skin: 50% higher response rate compared to control (RR 1.50; 95% CI, 1.33-1.70; P < .001)
Atopic Dermatitis: Diagnosis and Treatment.
(Full Study)Summary:Atopic dermatitis is a common chronic skin condition affecting 10% of people in their lifetime, characterized by itchy skin lesions. Treatment typically includes moisturizers, gentle cleansers, and topical corticosteroids as first-line therapy, with newer treatments available for more severe cases.Study TypeReviewStudied Populationgeneral population with atopic dermatitisResults
Long‐term safety of crisaborole ointment 2% in children and adults with mild to moderate atopic dermatitis
(Full Study)Summary:Crisaborole ointment showed good safety when used for up to 48 weeks, with most side effects being mild and not related to the treatment.Study TypeObservationalStudied Population517 children and adults (≥2 years) with mild to moderate atopic dermatitisResults
Crisaborole Topical Ointment, 2% in Patients Ages 2 to 17 Years with Atopic Dermatitis: A Phase 1b, Open‐Label, Maximal‐Use Systemic Exposure Study
(Full Study)Summary:Crisaborole 2% ointment applied twice daily was found to be safe with limited absorption into the body, and helped improve eczema symptoms in children aged 2-17 years when applied for 28 days.Study TypeObservationalStudied Population34 children ages 2-17 years with mild to moderate AD involving 25% or more treatable body surface areaResultsISGA change from baseline: -1.5
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Zoryve (Roflumilast)If your child is 6+ years and looking for a non-steroidal cream with good tolerabilityIf you are looking for a non-steroidal cream with good tolerabilityTopical once dailyHigh
Side Effect Affected Application site pain 1% Rash 1% Study Summary Study Type Studied Population Results -
Treatment:Zoryve (Roflumilast)Effectiveness:Who is this for?:If you are looking for a non-steroidal cream with good tolerabilityIf your child is 6+ years and looking for a non-steroidal cream with good tolerabilitySide Effects:Cost:-Delivery:Topical once dailyStudies
Off-label
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CellCept (Mycophenolate mofetil)NoneIf you have widespread flareups and topicals don't work for youOral daily
Side Effect Affected Study Summary Study Type Studied Population Results -
Treatment:CellCept (Mycophenolate mofetil)Effectiveness:Who is this for?:If you have widespread flareups and topicals don't work for youNoneSide Effects:Cost:-Delivery:Oral dailyStudies
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Gengraf, Neoral (Cyclosporine)NoneIf other treatments don't work for you and you are looking for relief within 1-2 weeksOral daily
Side Effect Affected Study Summary Study Type Studied Population Results -
Treatment:Gengraf, Neoral (Cyclosporine)Effectiveness:Who is this for?:If other treatments don't work for you and you are looking for relief within 1-2 weeksNoneSide Effects:Cost:-Delivery:Oral dailyStudies
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Otrexup, Rasuvo, Trexall, Xatmep, … (Methotrexate)NoneIf you have severe eczema that affects a large part of your body and doesn't respond well to steroids['oral', 'injection'] daily
Side Effect Affected Study Summary Study Type Studied Population Results -
Treatment:Otrexup, Rasuvo, Trexall, Xatmep, … (Methotrexate)Effectiveness:Who is this for?:If you have severe eczema that affects a large part of your body and doesn't respond well to steroidsNoneSide Effects:Cost:-Delivery:['oral', 'injection'] dailyStudies
Supplement
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Vitamin D3 (Cholecalciferol)If your child's symptoms get worse during winter or your child has confirmed low Vitamin D levelsIf your symptoms get worse during winter or you have confirmed low Vitamin D levelsOral dailyLow
Side Effect Affected None reported Study Summary Study Type Studied Population Results -
Treatment:Vitamin D3 (Cholecalciferol)Effectiveness:Who is this for?:If your symptoms get worse during winter or you have confirmed low Vitamin D levelsIf your child's symptoms get worse during winter or your child has confirmed low Vitamin D levelsSide Effects:Cost:-Delivery:Oral 1000-4000 IU dailyStudies
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Probiotics (Lactobacillus, Bifidobacterium)As a complementary treatment for children with moderate atopic dermatitisAs a complementary treatment alongside standard therapiesOral dailyHigh
Side Effect Affected No significant side effects reported Study Summary Study Type Studied Population Results -
Treatment:Probiotics (Lactobacillus, Bifidobacterium)Effectiveness:Who is this for?:As a complementary treatment alongside standard therapiesAs a complementary treatment for children with moderate atopic dermatitisSide Effects:Cost:-Delivery:Oral dailyStudies
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Vitamin B12 (Cobalamin)As an add-on alongside other therapiesAs an add-on alongside other therapiesOral daily
Side Effect Affected Study Summary Study Type Studied Population Results -
Treatment:Vitamin B12 (Cobalamin)Effectiveness:Who is this for?:As an add-on alongside other therapiesAs an add-on alongside other therapiesSide Effects:Cost:-Delivery:Oral dailyStudies
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Omega-3 (Polyunsaturated fatty acid)As a supplement to other treatmentsAs a supplement to other treatments, especially during pregnancy and breastfeedingOral daily
Side Effect Affected Study Summary Study Type Studied Population Results -
Treatment:Omega-3 (Polyunsaturated fatty acid)Effectiveness:Who is this for?:As a supplement to other treatments, especially during pregnancy and breastfeedingAs a supplement to other treatmentsSide Effects:Cost:-Delivery:Oral None dailyStudies
Other
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Coconut Oil (Virgin Coconut Oil)If you are looking for a gentle and natural moisturizer for your child that may help reduce inflammation and bacterial colonizationIf you are looking for a gentle and natural moisturizer that may help reduce inflammation and bacterial colonizationTopical dailyLow
Side Effect Affected Skin irritation Study Summary Study Type Studied Population Results -
Treatment:Coconut Oil (Virgin Coconut Oil)Effectiveness:Who is this for?:If you are looking for a gentle and natural moisturizer that may help reduce inflammation and bacterial colonizationIf you are looking for a gentle and natural moisturizer for your child that may help reduce inflammation and bacterial colonizationSide Effects:Cost:-Delivery:Topical as needed dailyStudies
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Oils (Other than coconut)If you are looking for a gentle and natural moisturizer that may help reduce inflammation and bacterial colonizationIf you are looking for a gentle and natural moisturizer that may help reduce inflammation and bacterial colonizationTopical daily
Side Effect Affected Study Summary Study Type Studied Population Results -
Treatment:Oils (Other than coconut)Effectiveness:Who is this for?:If you are looking for a gentle and natural moisturizer that may help reduce inflammation and bacterial colonizationIf you are looking for a gentle and natural moisturizer that may help reduce inflammation and bacterial colonizationSide Effects:Cost:-Delivery:Topical dailyStudies