๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-26

A Dose-ranging Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Galvokimig in Adult Study Participants With Atopic Dermatitis (NCT07277660)

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Ranging Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Galvokimig in Adult Study Participants With Moderate to Severe Atopic Dermatitis

๐ŸŸข Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: UCB Biopharma SRL

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The purpose of the study is to evaluate the dose-response relationship of galvokimig compared with placebo in study participants with moderate-to-severe atopic dermatitis (AtD).

Who can join: Review the eligibility criteria below.

Location: Atd002 52021 โ€” Oceanside, California

Age range: 18 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (68 Sites)

Showing the first 25 of 68 sites.

  • Atd002 52021 โ€” Oceanside, California
  • Atd002 52008 โ€” Santa Monica, California
  • Atd002 52013 โ€” Boca Raton, Florida
  • Atd002 52007 โ€” Miami, Florida
  • Atd002 52003 โ€” Miami, Florida
  • Atd002 52015 โ€” Savannah, Georgia
  • Atd002 52017 โ€” Chicago, Illinois
  • Atd002 52018 โ€” Wheaton, Illinois
  • Atd002 52012 โ€” New Albany, Indiana
  • Atd002 52014 โ€” Bowling Green, Kentucky
  • Atd002 52001 โ€” Troy, Michigan
  • Atd002 52009 โ€” Troy, Michigan
  • Atd002 52010 โ€” Omaha, Nebraska
  • Atd002 52022 โ€” New York, New York
  • Atd002 52020 โ€” The Bronx, New York
  • Atd002 52019 โ€” Philadelphia, Pennsylvania
  • Atd002 52005 โ€” Dallas, Texas
  • Atd002 52016 โ€” Frisco, Texas
  • Atd002 52011 โ€” Frisco, Texas
  • Atd002 52004 โ€” Sugar Land, Texas
  • Atd002 41004 โ€” Lovech,
  • Atd002 41001 โ€” Pleven,
  • Atd002 41007 โ€” Plovdiv,
  • Atd002 41002 โ€” Sevlievo,
  • Atd002 41003 โ€” Sofia,

๐Ÿ“ž Contact the Study Coordinator

Phone: (844) 599-2273

Email: ucbcares@ucb.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—