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Phase 2A/B Efficacy and Safety of Dabogratinib in Participants With Low Grade Upper Tract Urothelial Carcinoma

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NCT07265947 · readout ≤ 1,534 d

Sponsored by Tyra Biosciences, Inc (industry) · TYRA — their whole pipeline →.

Phase
Phase 2
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
230estimated
Sites
17
Countries
Spain, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-12-22actualWhen the study began enrolling
Primary completionOct 2030estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionNov 2030estimatedThe whole study's end, after follow-up
First posted2025-12-05actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-03actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Low Grade Upper Tract Urothelial Carcinoma

Interventions

  • Drug: Dabogratinib (TYRA-300) 60mg — also filed as TYRA-300
  • Drug: Dabogratinib (TYRA-300) 80mg — also filed as TYRA-300
  • Drug: Dabogratinib (TYRA-300) TBD — also filed as TYRA-300

Primary outcome

what the primary-completion date above is the date OF
To assess the efficacy of Dabogratinib in LG UTUC FGFR3+ participants (proportion of participants with a CR within 6 months out of all LG UTUC FGFR3+ participants)
measured within 6 months

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