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Safety and Preliminary Anti-Tumor Activity of TYRA-430 in Advanced Hepatocellular Carcinoma and Other Solid Tumors With Activating FGF/FGFR Pathway Aberrations
NCT06915753 · View on ClinicalTrials.gov ↗
Study Summary
A Phase 1 study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamic (PD), and preliminary antitumor activity of TYRA-430 in cancers with FGF/FGFR pathway aberrations, including locally advanced/metastatic hepatocellular carcinoma and other advanced solid tumors.
Conditions Studied
Interventions
- DRUG TYRA-430
Study Locations (16)
Other
- Asan Medical Center — Seoul
- Samsung Medical Center — Seoul
- Seoul National University Hospital — Seoul
- Severance Hospital, Yonsei University Health System — Seoul
- National Taiwan University Hospital — Taipei
- Taipei Veterans General Hospital — Taipei
California
- USC Norris Comprehensive Cancer Center — Los Angeles
- UCSF Medical Center at Mount Zion — San Francisco
- Stanford Cancer Institute — Stanford
Kansas
- The University of Kansas Medical Center — Westwood
Maryland
- John Hopkins University — Baltimore
Massachusetts
- Mass General Cancer Center — Boston
Michigan
- Karmanos Cancer Institute — Detroit
New York
- Columbia University Irving Medical Center — New York
Tennessee
- Sarah Cannon Research Institute Oncology Partners — Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2025-04-24 |
| Est. Completion | 2028-09 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06915753
The ClinicalTrials.gov registry entry for NCT06915753 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 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tyra Biosciences, which has 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 10 conditions, with Advanced Solid Tumors appearing as the primary indexed condition, and to 1 intervention — of which TYRA-430 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: NCT06915753 reports 16 study locations spanning 9 distinct geographic areas — top geographies include Other, California, Kansas. 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 NCT06915753 about?
NCT06915753 is a clinical study titled "Safety and Preliminary Anti-Tumor Activity of TYRA-430 in Advanced Hepatocellular Carcinoma and Other Solid Tumors With Activating FGF/FGFR Pathway Aberrations". A Phase 1 study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamic (PD), and preliminary antitumor activity of TYRA-430 in cancers with FGF/FGFR pathway aberrations, including locally advanced/metastatic hepatocellular carcinoma and other advanced solid tumors.
What is the current status of trial NCT06915753?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 100 participants. The study started on 2025-04-24. Estimated completion is 2028-09.
What conditions does trial NCT06915753 study?
This clinical trial studies the following conditions: Advanced Solid Tumors, Solid Tumors, Solid Tumor, Adult, Metastatic Hepatocellular Carcinoma, FGFR3 Gene Mutation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06915753?
The interventions under investigation include: TYRA-430 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06915753?
This trial is sponsored by Tyra Biosciences, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06915753 being conducted?
This trial has 16 study locations across California, Kansas, Maryland, Massachusetts, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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