🏛️ Verified NIH Record • Updated 2026-06-12
A Study of PATAS Trifluoroacetate Using Single Ascending Doses in Healthy Volunteers (NCT07223333)
First-in-Human, Randomized, Double-Blind, Placebo-Controlled Study of Single Ascending Doses in Healthy Volunteers to Evaluate the Safety, Tolerability, and Pharmacokinetics of PATAS
🔵 Active, Not Recruiting Phase1 💊 Investigational Drug / Biologic Sponsor: AdipoPharma LLC
🩺 Plain-English Summary (8th-Grade Level)
The primary objective of this study is to evaluate safety and tolerability of single subcutaneous (SC) doses of PATAS in healthy subjects. The secondary objective of this study is to determine the pharmacokinetics (PK) of single SC doses of PATAS in healthy subjects.
Who can join: Review the eligibility criteria below.
Location: Medpace Clinical Pharmacology Unit — Cincinnati, Ohio
Age range: 18 Years to 55 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 (2 Sites)
- Medpace Clinical Pharmacology Unit — Cincinnati, Ohio
- Medpace Clinical Pharmaology Unit — Cincinnati, Ohio
💰 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.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.