πŸ›οΈ Verified NIH Record β€’ Updated 2026-06-26

A Study of PYX-201 in Advanced Solid Tumors (NCT05720117)

A First-in-Human, Open-label, Multicenter, Phase 1 Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of PYX-201 in Participants With Advanced Solid Tumors

🟒 Recruiting Phase1 πŸ’Š Investigational Drug / Biologic Sponsor: Pyxis Oncology, Inc

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

The primary objectives of this study are to determine the recommended dose(s) of PYX-201 for participants with recurrent/metastatic (R/M) solid tumors, and to determine the objective response rate (ORR) in participants treated with PYX-201 as a single agent.

Who can join: Review the eligibility criteria below.

Location: HonorHealth Research Institute β€” Scottsdale, Arizona

Age range: 18 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (29 Sites)

Showing the first 25 of 29 sites.

  • HonorHealth Research Institute β€” Scottsdale, Arizona
  • Ronald Reagan UCLA Medical Center β€” Los Angeles, California
  • SCRI - HealthOne Denver β€” Denver, Colorado
  • SCRI - Florida Cancer Specialists β€” Sarasota, Florida
  • Winship Cancer Institute, Emory University β€” Atlanta, Georgia
  • University of Chicago Medicine β€” Chicago, Illinois
  • Massachusetts General Hospital β€” Boston, Massachusetts
  • Dana-Farber Cancer Institute β€” Boston, Massachusetts
  • Washington University School of Medicine β€” St Louis, Missouri
  • Memorial Sloan Kettering Cancer Center β€” New York, New York
  • University of Cincinnati Medical Center β€” Cincinnati, Ohio
  • University of Pennsylvania, Abramson Cancer Center β€” Philadelphia, Pennsylvania
  • Rhode Island Hospital β€” Providence, Rhode Island
  • NEXT Dallas β€” Dallas, Texas
  • The University of Texas MD Anderson Cancer Center β€” Houston, Texas
  • NEXT San Antonio β€” San Antonio, Texas
  • NEXT Virginia β€” Fairfax, Virginia
  • Institut Jules Bordet β€” Brussels, Brussels Capital
  • Cliniques Universitaires Saint-Luc β€” Brussels, Brussels Capital
  • Universitair Ziekenhuis Antwerpen β€” Edegem, Edegem
  • Universitair Ziekenhuis Gent β€” Ghent, Gent
  • Hospital Universitari Vall d'HebrΓ³n β€” Barcelona, Barcelona
  • START Madrid - Hospital Universitario FundaciΓ³n JimΓ©nez DΓ­az β€” Madrid, Madrid
  • Hospital Universitario 12 de Octubre β€” Madrid, Madrid
  • Hospital Universitario HM Sanchinarro β€” Madrid, Madrid

πŸ“ž Contact the Study Coordinator

Phone: (339) 545-8252

Email: clinicaltrials@pyxisoncology.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° 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 Β§ 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.

Explore by condition: All Solid Tumor clinical trials

πŸ’‘ 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.
πŸ›οΈ View Official NIH Record β†—