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RecruitingNCT07230405

A Phase II Study of SKB571 in Patients With Lung Cancer

A Phase II Study to Evaluate the Safety and Efficacy of SKB571 in Patients With Advanced Non-small Cell Lung Cancer

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
190 (estimated)
Sponsor
Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This is a multicenter, phase II study. The purpose of this study is to evaluate the safety and preliminary anti-tumor activity of SKB571 in patients with advanced non-small cell lung cancer. Eligible subjects will receive SKB571 monotherapy, until radiographic disease progression, intolerable toxicity, discontinuation of study treatment required by the subject, or other protocol-specified treatment discontinuation criteria, whichever occurs first.

Conditions

Interventions

TypeNameDescription
DRUGSKB571 for injectionSKB571 for injection is administered every 3 weeks(Q3W) until radiographic disease progression,intolerable toxicity, or other protocol-specified treatment discontinuation criteria, whichever occurs first.

Timeline

Start date
2026-01-19
Primary completion
2028-01-19
Completion
2028-01-19
First posted
2025-11-17
Last updated
2026-02-06

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT07230405. Inclusion in this directory is not an endorsement.

A Phase II Study of SKB571 in Patients With Lung Cancer (NCT07230405) · Clinical Trials Directory