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Phase 1/2 Study of PYX-201 in Combination With Pembrolizumab in Advanced Solid Tumors
NCT06795412 · View on ClinicalTrials.gov ↗
Study Summary
The primary objective of this study is to determine the recommended Phase 2 doses (RP2D(s)) and maximum tolerated dose (MTD) of PYX-201 in combination with pembrolizumab for participants with advanced solid tumors.
Conditions Studied
Interventions
- DRUG pembrolizumab
- DRUG PYX-201
Study Locations (15)
Madrid
- Hospital Universitario Ramón y Cajal — Madrid
- START Madrid - Hospital Universitario Fundación Jiménez Díaz — Madrid
- Hospital Universitario 12 de Octubre — Madrid
California
- University of California San Diego — San Diego
- Sarcoma Oncology Center — Santa Monica
Massachusetts
- Massachusetts General Hospital — Boston
- Dana-Farber Cancer Institute — Boston
Pennsylvania
- University of Pennsylvania — Philadelphia
- University of Pittsburgh Medical Center — Pittsburgh
Texas
- University of Texas - M.D. Anderson Cancer Center — Houston
- NEXT Oncology Houston — Houston
Florida
- Moffitt Cancer Center — Tampa
Virginia
- NEXT Virginia — Fairfax
Barcelona
- Hospital Universitario Vall d'Hebron — Barcelona
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 220 participants |
| Start Date | 2025-04-15 |
| Est. Completion | 2027-12-06 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06795412
The ClinicalTrials.gov registry entry for NCT06795412 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 220 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pyxis Oncology, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Advanced Solid Tumours appearing as the primary indexed condition, and to 2 interventions — of which pembrolizumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06795412 reports 15 study locations spanning 9 distinct geographic areas — top geographies include Madrid, California, Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06795412 about?
NCT06795412 is a clinical study titled "Phase 1/2 Study of PYX-201 in Combination With Pembrolizumab in Advanced Solid Tumors". The primary objective of this study is to determine the recommended Phase 2 doses (RP2D(s)) and maximum tolerated dose (MTD) of PYX-201 in combination with pembrolizumab for participants with advanced solid tumors.
What is the current status of trial NCT06795412?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 220 participants. The study started on 2025-04-15. Estimated completion is 2027-12-06.
What conditions does trial NCT06795412 study?
This clinical trial studies the following conditions: Advanced Solid Tumours. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06795412?
The interventions under investigation include: pembrolizumab (DRUG), PYX-201 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06795412?
This trial is sponsored by Pyxis Oncology, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06795412 being conducted?
This trial has 15 study locations across California, Florida, Massachusetts, Pennsylvania, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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