Efficacy and Safety of Ribupatide in Participants Living With Obesity or Overweight With Weight-Related Comorbidities Who Do Not Have Diabetes (NCT07284875)
A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of KAI-9531 Administered Once Weekly in Participants Living With Obesity or Overweight With Weight-Related Comorbidities Who Do Not Have Diabetes
π©Ί Plain-English Summary (8th-Grade Level)
The primary objective of the study is to determine the effects of ribupatide (KAI-9531) subcutaneous (SC) injection once weekly compared to placebo on percent change in body weight.
Who can join: Review the eligibility criteria below.
Location: Kailera Clinical Site β Anniston, Alabama
Age range: 18 Years
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π All Participating Trial Locations (88 Sites)
Showing the first 25 of 88 sites.
- Kailera Clinical Site β Anniston, Alabama
- Kailera Clinical Site β Birmingham, Alabama
- Kailera Clinical Site β Cullman, Alabama
- Kailera Clinical Site β Sun City, Arizona
- Kailera Clinical Site β Escondido, California
- Kailera Clinical Site β Toluca Lake, California
- Kailera Clinical Site β Aurora, Colorado
- Kailera Clinical Site β Bridgeport, Connecticut
- Kailera Clinical Site β Jupiter, Florida
- Kailera Clinical Site β Lilburn, Georgia
- Kailera Clinical Site β Springfield, Illinois
- Kailera Clinical Site β Columbia, Maryland
- Kailera Clinical Site β Las Vegas, Nevada
- Kailera Clinical Site β Rochester, New York
- Kailera Clinical Site β Morehead City, North Carolina
- Kailera Clinical Site β Chickasha, Oklahoma
- Kailera Clinical Site β Mauldin, South Carolina
- Kailera Clinical Site β Chattanooga, Tennessee
- Kailera Clinical Site β Amarillo, Texas
- Kailera Clinical Site β Bellaire, Texas
- Kailera Clinical Site β DeSoto, Texas
- Kailera Clinical Site β Tomball, Texas
- Kailera Clinical Site β Salt Lake City, Utah
- Kailera Clinical Site β Danville, Virginia
- Kailera Clinical Site β San NicolΓ‘s de los Arroyos, Buenos Aires
π Contact the Study Coordinator
Phone: (781) 317-0291
Email: info-clinicalstudies@kailera.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
π° 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 Β§ 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.
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π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.