RecruitingPhase 1NCT06915753

Safety and Preliminary Anti-Tumor Activity of TYRA-430 in Advanced Hepatocellular Carcinoma and Other Solid Tumors With Activating FGF/FGFR Pathway Aberrations

A Multicenter, Open-label, First-in-Human Study of TYRA-430 in Advanced Hepatocellular Carcinoma and Other Solid Tumors With Activating FGF/FGFR Pathway Aberrations


Sponsor

Tyra Biosciences, Inc

Enrollment

100 participants

Start Date

Apr 24, 2025

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing an experimental drug called TYRA-430 in patients with advanced liver cancer (hepatocellular carcinoma) or other solid tumors that have specific changes in a growth signaling pathway called FGF/FGFR. Researchers want to see if the drug is safe and shows early signs of fighting the cancer. **You may be eligible if...** - You are 18 or older with good performance status (ECOG 0-1) - You have advanced, unresectable liver cancer or another advanced solid tumor with FGF/FGFR pathway changes confirmed by testing - You have already received standard-of-care treatments for your cancer - Your liver, kidney, and blood counts are within acceptable ranges - You are able to swallow oral medications **You may NOT be eligible if...** - Your liver cancer is at an early or intermediate stage still eligible for localized treatment - Your liver function is significantly impaired (Child-Pugh class B or C) - You have untreated brain metastases or other serious active conditions Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTYRA-430

Oral TYRA-430 given daily.


Locations(16)

USC Norris Comprehensive Cancer Center

Los Angeles, California, United States

UCSF Medical Center at Mount Zion

San Francisco, California, United States

Stanford Cancer Institute

Stanford, California, United States

The University of Kansas Medical Center

Westwood, Kansas, United States

John Hopkins University

Baltimore, Maryland, United States

Mass General Cancer Center

Boston, Massachusetts, United States

Karmanos Cancer Institute

Detroit, Michigan, United States

Columbia University Irving Medical Center

New York, New York, United States

Sarah Cannon Research Institute Oncology Partners

Nashville, Tennessee, United States

University Health Network Princess Margaret Cancer Center

Toronto, Ontario, Canada

Asan Medical Center

Seoul, South Korea

Samsung Medical Center

Seoul, South Korea

Seoul National University Hospital

Seoul, South Korea

Severance Hospital, Yonsei University Health System

Seoul, South Korea

National Taiwan University Hospital

Taipei, Taiwan

Taipei Veterans General Hospital

Taipei, Taiwan

View Full Details on ClinicalTrials.gov

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NCT06915753


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