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

Recruiting Phase 2 Interventional Study
Advanced NSCLC
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
66 (estimated)
Sponsor
Shanghai Junshi Bioscience Co., Ltd. · Other
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About This Trial

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.

Trial Locations
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Eligibility Criteria
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 …
Contacts

Xiaojun Wang, Master

021-50796193

xiaojun_wang@junshipharma.com

CONTACT