๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-13

Study to Evaluate HM15275 in Subjects With Type 2 Diabetes Mellitus (NCT07527650)

A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Evaluate Efficacy, Safety, and Tolerability of HM15275 for 36 Weeks in Subjects With Type 2 Diabetes Mellitus

๐ŸŸข Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Hanmi Pharmaceutical Company Limited

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

This study is a Phase 2 clinical trial to evaluate the efficacy, safety, and tolerability of HM15275 in subjects with type 2 diabetes mellitus over 36 weeks.

Who can join: Review the eligibility criteria below.

Location: Desert Clinical Research โ€” Mesa, Arizona

Age range: 18 Years to 75 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 (15 Sites)

  • Desert Clinical Research โ€” Mesa, Arizona
  • Accel Research Sites - DeLand โ€” DeLand, Florida
  • Charter Research โ€” Orlando, Florida
  • AdventHealth Translational Research Institute โ€” Orlando, Florida
  • K2 Medical Research The Villages LLC โ€” The Villages, Florida
  • Centricity Research IRT - DBA IACT Health Columbus Piedmont โ€” Columbus, Georgia
  • The South Bend Clinic โ€” South Bend, Indiana
  • Jefferson City Medical Center โ€” Jefferson City, Missouri
  • Clay Platte Family Medicine โ€” Kansas City, Missouri
  • Methodist Physicians Clinic โ€” Fremont, Nebraska
  • Santa Rosa Medical Centers of Nevada โ€” Las Vegas, Nevada
  • Lucas Research, Inc. โ€” Morehead City, North Carolina
  • Centricity Research Columbus โ€” Columbus, Ohio
  • Olympus Family Medicine โ€” Salt Lake City, Utah
  • Manassas Clinical Research Center โ€” Manassas, Virginia

๐Ÿ“ž Contact the Study Coordinator

Phone: (822) 410-9147

Email: pureun.nam@hanmi.co.kr

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†—