🏛️ Verified NIH Record • 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

🟢 Recruiting Phase2 💊 Investigational Drug / Biologic Sponsor: Hanmi Pharmaceutical Company Limited

🩺 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 — Mesa, Arizona

Age range: 18 Years to 75 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (15 Sites)

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

📞 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.

💰 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 § 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.

💡 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.
🏛️ View Official NIH Record ↗