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ACTIVE NOT RECRUITING
NCT05906537
PHASE1

SKB410 for Injection in Solid Tumors

Sponsor: Sichuan Kelun Pharmaceutical Research Institute Co., Ltd.

View on ClinicalTrials.gov

Summary

This is a multicenter, open-label, multiple-dose dose finding and expansion study to evaluate the safety, tolerability, pharmacokinetic(PK) profile, and anti-tumor efficacy of SKB410 for injection in patients with advanced solid tumors.

Official title: A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of SKB410 for Injection in Subjects With Advanced Solid Tumors

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

54

Start Date

2023-06-30

Completion Date

2026-06-30

Last Updated

2025-08-07

Healthy Volunteers

No

Interventions

DRUG

SKB410 for injection

SKB410 for injection is administered every 2 weeks (q2w) until radiographic disease progression (PD), intolerable toxicity, death, or discontinuation of treatment, whichever occurs first.

Locations (1)

Beijing Cancer Hospital

Beijing, Beijing Municipality, China