A Study to Learn About Study Medicine Called PF-08049820 in People With Eczema
Pfizer · NCT07216027
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–64 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 2
- Target enrollment
- 165
- US sites recruiting
- 14
- Study start
- November 20, 2025
- Record last updated
- October 13, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this study is to learn if the study medicine (PF-08049820) is safe and effective for the treatment of atopic dermatitis (AD), also known as eczema, or atopic eczema. People with this condition may have severe itching and rashes on the skin.
The study is seeking participants who
- Are 18 to 64 years of age;
- Were confirmed to have AD at least 6 months ago;
- Do not have a suitable prescribed medicine for AD;
- Are considered by their doctors to have moderate to severe AD.
The study has two stages (Stage 1 and Stage 2). In both stages, eligible participants will take either PF-08049820 or placebo as tablets by mouth daily for 12 weeks. A placebo does not have any medicine in it but looks just like the medicine being studied. Participants will visit the clinic on Day 1, Weeks 1, 2, 4, 6, 8 and 12. They will have a follow-up visit at Week 16. During this time, the participant's health and skin condition will be checked. They will have blood and urine tests. They will also have to answer questions about their health, skin condition, and how much their skin condition affects their lives. The experiences of participants receiving the study medicine will be compared to those receiving placebo. This will help to understand if PF-08049820 is safe and effective.
Being studied: PF-08049820; Placebo
Conditions: Atopic Dermatitis; Eczema, Atopic
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
Participants must meet the following criteria:
- Are 18 to 64 years of age
- Have clinical diagnosis of AD for at least 6 months prior to Day 1 and have diagnosis of AD confirmed by photographs
- Have moderate to severe AD as defined by the following at screening and baseline visits:
- Affected body surface area (BSA) greater than or equal to 10% and up to 60%;
- Validated Investigator's Global Assessment (vIGA) greater than or equal to 3;
- Eczema Area and Severity Index (EASI) greater than or equal to 16;
AND
-Peak Pruritis Numeric Rating Scale (PP-NRS) greater than or equal to 4 at screening and a weekly average of greater than or equal to 4 at baseline visit
- Do not have a suitable prescribed medicine for AD.
- Body Mass Index (BMI) of 18 to 38 kg/m2 and a total body weight greater than 48 kg (106 lbs)
Exclusion Criteria
Participants must not meet the following criteria:
- Have an infection that requires treatment
- Have other skin conditions other than AD
- Have severe uncontrolled asthma
- Regular use (more than 2 visits per week) of a tanning booth or phototherapy for AD within 4 weeks of the screening visit
Recruiting US locations
Mayo Clinic Hospital
Phoenix, AZ 85054
Mayo Clinic Specialty Building
Phoenix, AZ 85054
Mayo Clinic
Scottsdale, AZ 85259
Marvel Clinical Research
Huntington Beach, CA 92647
Northridge Clinical Trials
Northridge, CA 91325
Clinical Science Institute
Santa Monica, CA 90403
Gsi Clinical Research
Margate, FL 33063
Montefiore - Jacobi Dermatology Clinic
The Bronx, NY 10461
Montefiore - Clinical Research Center
The Bronx, NY 10467
Montefiore - Greene Medical Arts Pavillion
The Bronx, NY 10467
Montefiore - The Dermatology Center
The Bronx, NY 10467
Montefiore Medical Center
The Bronx, NY 10467
Paddington Testing Co, Inc
Philadelphia, PA 19103
UPMC Department of Dermatology
Pittsburgh, PA 15213
Study contacts (from the official record)
- Pfizer CT.gov Call Center · 1-800-718-1021 · ClinicalTrials.gov_Inquiries@pfizer.com
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