🏛️ Verified NIH Record • Updated 2026-07-24

Usnoflast Neuromuscular Investigation for Treatment Efficacy in Amyotrophic Lateral Sclerosis (NCT07023835)

A Phase 2b, Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Usnoflast Administered to Adult Subjects With ALS

🟢 Recruiting Phase2 💊 Investigational Drug / Biologic Sponsor: Zydus Therapeutics Inc.

🩺 Plain-English Summary (8th-Grade Level)

Usnoflast Neuromuscular Investigation for Treatment Efficacy in Amyotrophic Lateral Sclerosis

Who can join: Review the eligibility criteria below.

Location: Zydus US015 — La Jolla, California

Age range: 18 Years

📋 "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 (17 Sites)

  • Zydus US015 — La Jolla, California
  • Zydus US008 — Orange, California
  • Zydus US013 — San Francisco, California
  • Zydus US005 — New Britain, Connecticut
  • Zydus US012 — Tampa, Florida
  • Zydus US007 — Atlanta, Georgia
  • Zydus US010 — Boston, Massachusetts
  • Zydus US006 — Detroit, Michigan
  • Zydus US014 — Lincoln, Nebraska
  • Zydus US003 — Winston-Salem, North Carolina
  • Zydus US009 — Pittsburgh, Pennsylvania
  • Zydus US001 — Dallas, Texas
  • Zydus US002 — Houston, Texas
  • Zydus US004 — Richmond, Virginia
  • Zydus US011 — Seattle, Washington
  • Zydus 101 — Toronto, Ontario
  • Zydus 100 — Québec, Quebec

📞 Contact the Study Coordinator

Phone: (609) 453-4751

Email: fshaikh@zydustherapeutics.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.

💡 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 ↗