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EB01 Cream 2.0% for Allergic Contact Dermatitis
Study Summary
This trial will test a new cream to see if it is safe and effective in treating people with a chronic allergic skin condition.
- Allergic Contact Dermatitis
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
Frequently Asked Questions
Is the demographic for this trial inclusive of individuals aged 70 or older?
"Candidates aged between 18 and 70 are viable for this trial; however, there is an additional 96 trials available to those below the age of majority, as well 156 studies appropriate for seniors above 65."
Are there any vacancies available in this clinical experiment?
"As per clinicaltrials.gov, this particular medical trial is no longer enrolling patients; the initial listing was posted on October 15th 2019 and last updated on September 9th 2022. Nevertheless, there are 221 other trials actively searching for participants at present."
How many sites are hosting the research for this experiment?
"Across the United States of America, 14 different clinical trial sites are currently in operation. Notable locations include Bexley Dermatology, The Dermatology Clinic found in Baton Rouge and Associated Skin care Specialists situated in Fridley."
Could you provide an assessment of the safety profile for EB01 Cream 2.0%?
"Due to the Phase 2 trial status of EB01 Cream 2.0%, our team at Power deemed its safety level as a score of two, implying that some evidence exists for its security but none yet for efficacy."
Is enrollment available for this medical experiment?
"This clinical trial is enrolling up to 126 individuals in the 18-70 age bracket who have allergic contact dermatitis. Additional requirements include: men and women of consenting age, those considered biologically able to bear children must use a reliable form contraception for at least 4 weeks pre and post study product application, surgical sterilization (hysterectomy/oophorectomy), cessation of menses for 12 months accompanied by an appropriate FSH test confirming nonchildbearing potential, male participants engaging in intercourse requiring contraceptive measures from Day 1 until 4 weeks after last study administration, negative pregnancy test for female childbearing potentials prior to screening"
Who else is applying?
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What portion of applicants met pre-screening criteria?
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