Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06807268

A Study of the Medicine Called Abrocitinib in Children 6 to Less Than 12 Years of Age With Moderate-to-Severe Eczema

A 16-WEEK, MULTICENTER, INTERVENTIONAL, PHASE 3, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL GROUP STUDY TO INVESTIGATE EFFICACY AND SAFETY OF ABROCITINIB IN CHILDREN 6 TO LESS THAN 12 YEARS OF AGE WITH MODERATE-TO-SEVERE ATOPIC DERMATITIS

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Pfizer · Industry
Sex
All
Age
6 Years – 11 Years
Healthy volunteers
Not accepted

Summary

This research study is being conducted to find out if the test medicine, abrocitinib, improves eczema and is safe for children 6 to \<12 years of age who have moderate-to-severe eczema. Research study participants who meet the study criteria will be assigned by chance (like the flip of a coin) to receive either abrocitinib test medicine or placebo (pretend medicine that looks just like the test medicine) for 16 weeks. The study will last for about 24 weeks in total.

Detailed description

Different questionnaires will be used to find out how the participant's eczema is doing during the research study. An electronic diary, which looks like a cellular phone, will be used to collect the questionnaire information and other research study-related information. It will also be used to remind participants to take the test medicine each day and to fill out the questionnaires. Participants will also be asked to wear something on their wrist that looks like a children's wristwatch so we can know when they are scratching their skin because of their atopic dermatitis. Laboratory tests, physical examinations and vital signs (height, weight, temperature, blood pressure and heart rate) will be conducted before and during the research study to monitor your child's health. Participants will need to come to the clinic for research study visits and at other times during the research study, the research study doctor or nurse will call the participants to find out the participant is doing.

Conditions

Interventions

TypeNameDescription
DRUGAbrocitinibAbrocitinib administered as liquid oral suspension.
OTHERPlaceboPlacebo administered as liquid oral suspension.

Timeline

Start date
2025-07-24
Primary completion
2027-05-02
Completion
2027-05-02
First posted
2025-02-04
Last updated
2026-04-07

Locations

40 sites across 8 countries: United States, China, Germany, Hungary, Japan, Mexico, Poland, Spain

Regulatory

Source: ClinicalTrials.gov record NCT06807268. Inclusion in this directory is not an endorsement.