🏛️ Verified NIH Record • Updated 2026-06-18
A Phase 2A Clinical Trial to Assess the Safety and Tolerability of ERX1000 in Men and Women for the Treatment of Obesity. (NCT07570758)
A Phase 2A, Randomized, Double-Blind, Placebo-Controlled, Clinical Study to Assess Efficacy, Safety and Tolerability of Orally Administered ERX1000 in Subjects With Obesity
🟢 Recruiting Phase2 💊 Investigational Drug / Biologic Sponsor: ERX Pharmaceuticals
🩺 Plain-English Summary (8th-Grade Level)
The primary objective is to assess the safety and tolerability of oral dose ERX1000 in obese subjects.
Who can join: Review the eligibility criteria below.
Location: Monroe Biomedical Research — Louisville, Kentucky
Age range: 18 Years to 60 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (3 Sites)
- Monroe Biomedical Research — Louisville, Kentucky
- Monroe Biomedical Research — Monroe, North Carolina
- Monroe Biomedical Research — North Charleston, South Carolina
📞 Contact the Study Coordinator
Phone: (908) 952-6877
Email: recruitment@monroeresearch.com
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.
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💡 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.