RecruitingPhase 2Phase 3NCT07662395

SCTB41 Combined With Chemotherapy in Advanced Squamous Non-Small Cell Lung Cancer

A Multicenter Phase II/III Study Evaluating the Efficacy and Safety of SCTB41 Combined With Chemotherapy Versus Tislelizumab Combined With Chemotherapy as First-Line Treatment for Driver-Negative Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)


Sponsor

Sinocelltech Ltd.

Enrollment

410 participants

Start Date

May 9, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This is a multicenter Phase II/III study evaluating the efficacy and safety of SCTB41 combined with chemotherapy versus tislelizumab combined with chemotherapy as first-line treatment in patients with driver-negative locally advanced or metastatic non-small cell lung cancer (NSCLC). The Phase II portion is an open-label safety run-in study enrolling approximately 30-60 patients to evaluate the safety and tolerability of SCTB41 plus chemotherapy. Following confirmation of acceptable safety and preliminary efficacy, the study will proceed to the Phase III portion. The Phase III portion is a randomized, double-blind, active-controlled study enrolling approximately 350 patients. Eligible participants will be randomized in a 1:1 ratio to receive SCTB41 plus chemotherapy or tislelizumab plus chemotherapy. The primary objective is to compare progression-free survival assessed by blinded independent central review according to RECIST version 1.1.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Carboplatin, a drug called Cisplatin, and others for people with double-blind. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSCTB41

IV infusion,Specified dose on specified days.

DRUGTislelizumab

IV infusion,Specified dose on specified days.

DRUGPaclitaxel

175 mg/m², IV infusion, Q3W, for 4 cycles.

DRUGNab-paclitaxel

100 mg/m², IV infusion, on Days 1, 8, 15 of each 3-week cycle, for 4 cycles

DRUGCarboplatin

AUC 5, IV infusion, Q3W, for 4 cycles.

DRUGCisplatin

75 mg/m², IV infusion, Q3W, for 4 cycles.

DRUGPemetrexed

500 mg/m², IV infusion, Q3W, for 4 cycles .


Locations(1)

Guangdong Provincial People's Hospital

Guangzhou, Guangdong, China

View Full Details on ClinicalTrials.gov

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NCT07662395


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