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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.

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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