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Clinical Trials in China / NCT06924606
Recruiting Phase 2

Evaluating the Preliminary Efficacy and Safety of JS207 in NSCLC After Progression Following Platinum-based Chemotherapy and Immunotherapy

NCT06924606 · tracked via the Priya Life Science China tracker
Sponsor
Shanghai Junshi Bioscience Co., Ltd.
Phase
Phase 2
Started
2025-07-15
Last updated
2026-02-06

Condition(s) studied

Advanced NSCLC

Investigational drug(s) / intervention(s)

JS207 injection +docetaxelJS207 injection +JS004 injectionJS207 injection

JS207 injection +docetaxel: Patients receive JS207 10mg/kg or other dosage and docetaxel 75mg/m2, q3w.

JS207 injection +JS004 injection: Patients receive JS207 10mg/kg or other dosage and JS004 200mg, q3w.

JS207 injection: Patients receive JS207 10mg/kg or other dosage.

Study summary

This is a multiple-arm, open phase II clinical trial evaluating the safety, tolerability,and preliminary efficacy of JS207 in NSCLC after progression following Platinum-based chemotherapy and immunotherapy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: 1. Histologically or cytologically confirmed locally advanced (stage IIIB/IIIC) NSCLC that is not amenable to radical surgery or radical radiochemotherapy, or Metastatic or recurrent NSCLC. 2. Subjects with unresectable locally advanced or metastatic or recurrent NSCLC who have failed first-line treatment with PD-1/PD-L1 inhibitors combined with platinum-based doublet chemotherapy (excluding docetaxel); or who have failed sequential first- and second-line treatment with PD-1/PD-L1 inhibitors followed by platinum-based doublet chemotherapy (excluding docetaxel). 3. Subjects must have at least one measurable lesion according to RECIST v1.1. Exclusion Criteria: 1. Histopathologically or cytopathologically confirmed to have combined neuroendocrine component. 2. Sensitivity mutation of EGFR or ALK fusion. 3. Tumor encircles important blood vessels or has obvious necrosis and air space, and the investigator considers that it may cause hemorrhage risk.

Primary outcome measure(s)

Trial sites (18)

FacilityCityRegionStatus
Beijing Chest Hospital, Capital Medical University Beijing Beijing Municipality Recruiting
Jilin Cancer Hospital Jilin City Changchun Recruiting
Hunan Cancer Hospital Hunan Changsha Recruiting
West China Hospital, Sichuan University Sichuan Chengdu Recruiting
Second Affiliated Hospital, PLA Academy of Military Medical Sciences Chongqing Chongqing Municipality Recruiting
Army Medical Center, PLA Chongqing Chongqing Municipality Recruiting
The First Affiliated Hospital of Guangzhou Medical University Guangdong Guangzhou Recruiting
Harbin Medical University Cancer Hospital Heilongjiang Harbin Recruiting
Anyang Tumor Hospital Anyang Henan Recruiting
The First Affiliated Hospital of Henan University of Science and Technology Luoyang Henan Recruiting
The First Affiliated Hospital of Xinxiang Medical University Xinxiang Henan Recruiting
The First People's Hospital of Changde Changde Hunan Recruiting
The First Affiliated Hospital of Nanchang University Jiangxi Nanchang Recruiting
Shanghai Pulmonary Hospital Shanghai Shanghai Municipality Recruiting
The Third People's Hospital of Datong Datong Shanxi Recruiting
Yibin Second People's Hospital Yibin Sichuan Recruiting
Affiliated Tumor Hospital of Xinjiang Medical University Xinjiang Xinjiang Recruiting
Shanghai Pulmonary Hospital Shanghai China Not Yet Recruiting

More Shanghai Junshi Bioscience Co., Ltd. trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06924606 on ClinicalTrials.gov ↗ ← All trials in China