๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-07-31

Open-Label Phase 1/2 Study of NEO-811 in Subjects With Locally Advanced or Metastatic Non-Resectable Clear Cell Renal Cell Carcinoma (NCT07300241)

An Open-Label, First-in-Human, Phase 1/2 Dose Escalation and Expansion Study of NEO-811 in Subjects With Locally Advanced or Metastatic Non-Resectable Clear Cell Renal Cell Carcinoma

๐ŸŸข Recruiting Phase1 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Neomorph, Inc

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

The NEO-811-101 study is an open-label, first-in-human, Phase 1/2 dose escalation and expansion study testing NEO-811, an ARNT molecular glue degrader, in subjects with locally advanced or metastatic non-resectable clear cell renal cell carcinoma. The study will test NEO-811 initially as a monotherapy.

Who can join: Review the eligibility criteria below.

Location: NEO-811 Los Angeles Site โ€” Duarte, California

Age range: 18 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 (12 Sites)

  • NEO-811 Los Angeles Site โ€” Duarte, California
  • NEO-811 San Diego Site โ€” San Diego, California
  • NEO-811 Connecticut Site โ€” New Haven, Connecticut
  • NEO-811 Chicago Site โ€” Zion, Illinois
  • NEO-811 Grand Rapids Site โ€” Grand Rapids, Michigan
  • NEO-811 Omaha Site โ€” Omaha, Nebraska
  • NEO-811 Long Island Site โ€” Lake Success, New York
  • NEO-811 NYC Site โ€” New York, New York
  • NEO-811 South Carolina Site โ€” Myrtle Beach, South Carolina
  • NEO-811 Dallas Site โ€” Dallas, Texas
  • NEO-811 Houston Site โ€” Houston, Texas
  • NEO-811 Virginia Site โ€” Fairfax, Virginia

๐Ÿ“ž Contact the Study Coordinator

Phone: (858) 428-9800

Email: clinicaltrials@neomorph.com

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†—