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

Study acronym: SURF303
StatusRecruiting
PhasePhase 2
Started

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Record History

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  1. Minor Enrollment increased: 230 → 285 participants
    • Interventions modified
    • Trial arms changed: 3 → 2
    • Eligibility criteria shortened, about 8 words
  2. Minor Re-verified, no change to tracked fields
  3. Minor Trial sites expanded: 26 → 32 locations
  4. Minor Eligibility criteria expanded, about 31 words
    • Site details revised at 1 of 26 sites
  5. Minor Trial sites expanded: 21 → 24 locationsv23
  6. Minor Study sites: 24 to 25v22
  7. Minor Trial sites expanded: 18 → 21 locationsv21
  8. Minor Study sites: 18 to 21v20
  9. Minor Study sites: 17 to 18v19
  10. Minor Study sites: 16 to 17v18
  11. Minor Re-verified, no change to tracked fieldsv17
  12. Minor Study sites: 15 to 16v16
  13. Minor Study sites: 14 to 15v15
  14. Minor Study sites: 13 to 14v14
  15. Minor Study sites: 12 to 13v13
  16. Minor Study sites: 11 to 12v12
  17. Minor Study sites: 10 to 11v11
  18. Minor Study sites: 9 to 10v10
  19. Minor Study sites: 7 to 9v9
  20. Minor Study sites: 6 to 7v8
  21. Minor Study sites: 5 to 6v7
  22. Minor Study sites: 4 to 5v6
  23. Minor Study sites: 3 to 4v5
  24. Minor Study sites: 2 to 3v4
  25. Minor Study sites: 1 to 2v3
  26. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date changed from estimate of Dec 2025 to Dec 22, 2025
    v2
  27. Minor Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
A Phase 2A/B study of Dabogratinib (TYRA-300) in Low Grade Upper Tract Urothelial Carcinoma
Trial Details
NCT Number NCT07265947
Lead Sponsor Tyra Biosciences, Inc
Conditions
(from sponsor)
Low Grade Upper Tract Urothelial Carcinoma
Enrollment 285 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov