Clinical Trial Search

Primary: Number of Wounds by Healing Category Per Investigator Visual Assessment — 35; 5; 2; 28 wounds

Primary: Foot Health Status Questionnaire, Foot Function Domain Score — 61.7; 49.3; 60.2; 56.3 score on a scale

Primary: Participants With Documented Complete Closure Of The Target Wound Within 1 Month After Initiation Of Treatment — 8; 6; 7; 7 Participants — p==0.3699

Primary: Intra-individual Difference in Reepithelialization of Wound (Halves) at Day 14 in 'Recent Wounds' or Day 28 in 'Chronic Wounds' — 8; 0 Wounds — p==0.008

Primary: Proportion of Patients With First Complete Closure of the EB Target Wound Within 45 Days of Treatment — 45; 33 Participants — p=0.013

Primary: Percentage of Grafts Successfully Treated — 78 Percentage of grafts

Primary: Blister/Erosion Reduction Based on Change in Body Surface Area (BSA) Coverage — 57.25; 39.40; 27.25; 25.45 percentage of BSA involvement

Primary: Percentage of Wound Surface Area Change From Baseline to Week 8 — -63; -8.1 percentage of wound surface area

Primary: Time To Complete Target Wound Closure Within 3 Months — 41.6; 53.6 days — p=0.985

Primary: Number of Wounds With Greater Than 90% Wound Closure at 4 Months — 0; 3 Wounds — p=0.21

Primary: Increased Expression of Full-length Type VII Collagen as Assessed by Immunofluorescence — 31.8; 28.4; 65.6 C7 Expression (percent of normal skin)

Primary: Percentage of Participants With Event-free Survival — 67; 80; 50; 29 Percentage of participants

Primary: Treatment-emergent Adverse Events — 40 Participants

Primary: Restoration of Full-length Type VII Collagen as Assessed by Immunofluorescence. — 5; 5; 4; 4 Fluorescence Intensity (MFI) for C7

Primary: Event-free Survival — 4; 2; 1 Count of Participants

Primary: Percent Change of Active Blisters and in Total Blister/Erosion Counts — -29.6 percent change — p=0.82

Primary: Number of Subjects Reported at Least One Adverse Event, Safety Population — 9 Participants

Primary: Comparative Weekly Change in NRS Itch Score Over the 8-week Active Treatment Period — -2; -1 score/week comparative change

Primary: Percent of Participants Achieving Sustained Remission at Week 36 — 4.0; 18.2 Estimated Percentage of Participants — p=0.0250

Primary: Number of Patients Who Achieve at Least a 3-point Reduction in AI-NRS. — 1; 3 Participants — p=0.59

Primary: Detectable Plasma Concentrations of Diacerein and Rhein — 3; 2; 0; 0 Participants

Primary: Number of Participants With Anti-Drug Antibodies — 0 Participants

Primary: Heterozygous for Filaggrin (FLG) Null Mutations — 1; 4 participants

Primary: Cessation of Blister Formation — NA days

Primary: Provider-diagnosed Atopic Dermatitis — 217.7; 268.5 Participants with imputed values — p=0.019

Primary: Assessment of Visual Analog Scale (VAS) Change (Values From 0 (Worst) to 10 (Best)) — 0; 50 Percentage reporting improvement

Primary: Median Time From First Dose of Omalizumab Treatment to Cessation of New Blisters. — 6 weeks

Primary: Primary Safety Endpoint — 0; 0; 1 participants

Primary: Percent Change From Baseline in Transepidermal Water Loss After 5 Skin Tape Stripping (STS) on Lesional Skin (LS) in AD Patients at Week 16 — -54.6 percent change…

Primary: Differences in Histologic Alterations in Rash Caused by Lapatinib, a Dual HER1/2 Inhibitor (HER1/2i), and the Single HER1 Inhibitors (HER1i) Cetuximab, Erlotinib,and…