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
π©Ί 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
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π 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
π 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.
π° 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.
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- A Study of RP-3500 in Combination With Standard Radiation Therapy in People With Solid Tumor Cancer β Basking Ridge, New Jersey
- Study of PD1 Blockade by Pembrolizumab With Stereotactic Body Radiotherapy in Advanced Solid Tumors β Chicago, Illinois
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π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.