Skip to content
Study details
Enrolling now

Safety and Preliminary Anti-Tumor Activity of TYRA-430

Tyra Biosciences, Inc
NCT IDNCT06915753ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

100

Study length

about 3.4 years

Ages

18+

Locations

9 sites in CA, KS, MA +4

What this study is about

Researchers are testing the safety, tolerability, and how well TYRA-430 works against cancer cells with FGF/FGFR pathway problems. The trial will last for about 1255 days.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take TYRA-430

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Maximum tolerated dose (MTD), Rate and severity of adverse events of TYRA-430 as monotherapy

Secondary: Cmax, Disease Control Rate (DCR), Duration of Response (DOR), Overall Response Rate (ORR), Time to Response (TTR), Tmax, t1/2

Body systems

Oncology