๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-24

A Study of ARV-393 in Relapsed/Refractory Non-Hodgkin Lymphoma. (NCT06393738)

A Phase 1 First in Human Study of ARV-393 in Adult Participants With Advanced Non-Hodgkin's Lymphoma

๐ŸŸข Recruiting Phase1 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Arvinas Inc.

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

This clinical trial is studying the safety and potential anti-tumor activity of an investigational drug called ARV-393 in patients diagnosed with advanced Relapsed/Refractory non-Hodgkin's lymphoma (R/R NHL) to determine if ARV-393 may be a possible treatment option. ARV-393 is thought to work by breaking down a protein present in many types of non-Hodgkins lymphomas, which may prevent, slow or stop tumor growth. This is the first time ARV-393 will be used by people. The investigational drug will be given as an oral tablet.

Who can join: Review the eligibility criteria below.

Location: Clinical Trial Site โ€” New Haven, Connecticut

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 (19 Sites)

  • Clinical Trial Site โ€” New Haven, Connecticut
  • Clinical Trial Site โ€” Miami, Florida
  • Clinical Trial Site โ€” Detroit, Michigan
  • Clinical Trial Site โ€” New Brunswick, New Jersey
  • Clinical Trial Site โ€” New York, New York
  • Clinical Trial Site โ€” New York, New York
  • Clinical Trial Site โ€” Cleveland, Ohio
  • Clinical Trial Site โ€” Nashville, Tennessee
  • Clinical Trial Site โ€” Houston, Texas
  • Clinical Trial Site โ€” Charlottesville, Virginia
  • Clinical Trial Site โ€” Toronto, Ontario
  • Clinical Trial Site โ€” Montreal, Quebec
  • Clinical Trial Site โ€” Copenhagen,
  • Clinical Trial Site โ€” Odense C,
  • Clinical Trial Site โ€” El Palmar, Murcia
  • Clinical Trial Site โ€” Pamplona, Navarre
  • Clinical Trial Site โ€” Barcelona,
  • Clinical Trial Site โ€” Madrid,
  • Clinical Trial Site โ€” Salamanca,

๐Ÿ“ž Contact the Study Coordinator

Phone: (475) 345-0791

Email: clinicaltrialsARV-393@arvinas.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†—