Clinical trial
An Open-label, First-in-Human, Dose-Escalation and Dose-Expansion Phase I/II Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of SPR1020 in Patients With Advanced Solid Tumors
NCT07359066 is registered in ClinicalTrials.gov with Shanghai SciBrunch Therapeutics Co., Ltd. as lead sponsor.
Search trials, sites, companies and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.
Registry record
As filed in ClinicalTrials.gov.
- Title
- An Open-label, First-in-Human, Dose-Escalation and Dose-Expansion Phase I/II Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of SPR1020 in Patients With Advanced Solid Tumors
- Lead sponsor
- Shanghai SciBrunch Therapeutics Co., Ltd.
- Phase
- Phase 1/2
- Overall status
- Recruiting
- Start date
- January 8, 2026
- Completion date
- June 30, 2028
- Enrollment
- 210 (estimated)
- Sites
- 2
Conditions
As the registry lists them; a condition with its own page is linked.
advanced solid tumors, parp inhibitor