← Eichor
Study identifier: NCT06564389 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

FIH Study to Evaluate the Tolerability of PF-07832837 in Healthy Adults and Patients

Condition: Healthy Participants · Atopic Dermatitis  ·  Sponsor: Pfizer

PhasePhase 1
Planned participants119
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersYes

About this study

The purpose of the study is to evaluate the safety, tolerability, and pharmacokinetics of escalating single and repeat doses of PF-07832837 in healthy participants and in participants with moderate to severe atopic dermatitis. An additional goal is to assess the pharmacodynamics of PF-07832837 in participants with moderate to severe AD, including potential effects on clinical signs and symptoms

This description comes directly from the study's public registry record.

Talk to the study team

Pfizer CT.gov Call Center  ·  1-800-718-1021  ·  ClinicalTrials.gov_Inquiries@pfizer.com

Always discuss trial participation with your own doctor first.

Locations (5)

Anaheim Clinical Trials, LLCAnaheim, California, United StatesRecruiting
TCR Medical CorporationSan Diego, California, United StatesRecruiting
Miami Dermatology and Laser ResearchMiami, Florida, United StatesRecruiting
Revival Research Institute, LLCTroy, Michigan, United StatesRecruiting
Paddington Testing CompanyPhiladelphia, Pennsylvania, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06564389