A Study to Evaluate How the Study Drug Moves Through the Body, Adverse Events, and How the Body Tolerates ABBV-547 Injections
Running, not enrolling · Phase 1 · Has a placebo group
Conditions studied: Healthy Volunteer
In brief
The purpose of this study is to assess how safe, effective, and tolerable ABBV-547 is in adult participants in the United States and Japan. There will be 2 parts to this study. In Part 1, participants are placed in one of 7 groups where they will receive ABBV-547 at different doses or placebo. There is a 1 in 4 chance participants will receive placebo. In Part 2, participants are placed in one of 3 groups where they will receive ABBV-547 at different doses or placebo. There is a 1 in 7 chance participants will receive placebo. Approximately 121 adult participants will be enrolled at approximately 21 sites in the United States and Japan. Participants will be administered one dose of ABBV-547 or placebo. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.
Key facts
- Study ID
- NCT07232004
- Run by
- AbbVie
- People needed
- 121
- Starts
- 2025-11-24
- Expected to finish
- 2027-08-01
- Last updated by the study team
- 2026-07-24
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- A condition of general good health, based upon the results of a medical history, physical examination, vital signs, laboratory profile and a 12-lead electrocardiogram (ECG).
- Part 1: BMI is >= 18.0 to <= 29.9 kg/m\^2 after rounding to the tenths decimal at Screening. BMI is calculated as weight in kg divided by the square of height measured in meters.
- Part 2: must have discontinued use of phototherapy (e.g., UVA or UVB) at least 2 weeks prior to the baseline visit (Day 1) and PUVA phototherapy at least 4 weeks prior to the baseline visit (Day 1).
You may not qualify if…
- History of any clinically significant sensitivity or allergy to any medication or food.
- Part 2: uses any herbal supplements within the 2-week period prior to study treatment administration.
- Part 2: received any biologics including investigational agents within 2.5 half-lives prior to Baseline.
Where it is running
- Total Dermatology /ID# 279798 — Birmingham, Alabama, United States
- Dermatology Trial Associates /ID# 279984 — Bryant, Arkansas, United States
- CenExel ACT- Anaheim Clinical Trials /ID# 279612 — Anaheim, California, United States
- Dermatology Research Associates - Los Angeles /ID# 279383 — Los Angeles, California, United States
- Integrative Skin Science and Research - Location 2 /ID# 279386 — Sacramento, California, United States
- Skin Care Research Boca Raton /ID# 279988 — Boca Raton, Florida, United States
- Wellness Clinical Research - Miami Lakes /ID# 279803 — Miami Lakes, Florida, United States
- Advanced Clinical Research Institute - Tampa /ID# 279342 — Tampa, Florida, United States
- Trueblue Clinical Research - Tampa /ID# 281757 — Tampa, Florida, United States
- University Dermatology & Vein Clinic - Darien /ID# 279986 — Darien, Illinois, United States
- Acpru /Id# 278638 — Grayslake, Illinois, United States
- MetroBoston Clinical Partners /ID# 279992 — Boston, Massachusetts, United States
- Minnesota Clinical Study Center /ID# 279987 — New Brighton, Minnesota, United States
- MediSearch Clinical Trials /ID# 279416 — Saint Joseph, Missouri, United States
- Skin Specialists /ID# 279531 — Omaha, Nebraska, United States
- The Skin Center Dermatology Group /ID# 279983 — New City, New York, United States
- Equity Medical, LLC - Bronx /ID# 279808 — The Bronx, New York, United States
- Oregon Dermatology and Research Center /ID# 279391 — Portland, Oregon, United States
- Health Concepts /ID# 279529 — Rapid City, South Dakota, United States
- Center for Clinical Studies - Houston - Binz Street /ID# 279419 — Houston, Texas, United States
- Austin Institute for Clinical Research - Pflugerville /ID# 279387 — Pflugerville, Texas, United States
- University of the Ryukyus Hospital /ID# 279918 — Ginowan-shi, Okinawa, Japan
- Fukuoka University Hospital /ID# 279530 — Fukuoka, Japan
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.