Biopharma Transcript

Tyra Biosciences, Inc. TYRA

Nasdaq · Phase 2 · oncology · small molecule · EDGAR · Updated Oct 24, 2026

Tyra Biosciences, Inc. (Nasdaq: TYRA) is an oncology drug developer. Its lead program, Dabogratinib (oral, formerly TYRA-300), is in Phase 2 for FGFR3-altered urothelial cancers (LG-UTUC, IR NMIBC) and achondroplasia. Its next catalyst on record is Dabogratinib BEACH301: Safety sentinel cohort results incl. 6-month annualized height velocity (March 2027).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: Dabogratinib BEACH301 — Safety sentinel cohort results incl. 6-month annualized height velocity (March 2027). 2 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
Dabogratinib SURF303Low-grade upper tract urothelial carcinomasmall moleculePhase 2
Dabogratinib SURF302Intermediate-risk NMIBCsmall moleculePhase 2
Dabogratinib BEACH301Achondroplasia in childrensmall moleculePhase 2
TYRA-430 (SURF431)FGF19+ hepatocellular carcinomasmall moleculePhase 1
TYRA-200 (SURF201)FGFR2-driven intrahepatic cholangiocarcinomasmall moleculePhase 1

Recent results and decisions

  1. Sep 9, 2026
    positive Initial SURF302 data: 60 mg QD ORR 79% (11/14) with 57% CR at 3 months; 50 mg QD ORR 67% (8/12); favorable safety, no Grade 4/5 TEAEs.The study provided clinical proof of concept for selective oral FGFR3 inhibition and identified 60 mg once-daily (QD) as the potential dose supporting TYRA’s planned registrational adjuvant development strategy. Filing

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