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

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 Details

NCT ID
NCT06924606
Phase
PHASE2
Sponsor
Shanghai Junshi Bioscience Co., Ltd.
Status
RECRUITING
Cancer Type
Lung Cancer
Interventions
  • JS207 injection +docetaxel
  • JS207 injection +JS004 injection
  • JS207 injection
Locations (sample)
  • Beijing, Beijing Municipality, China|39.9075,116.39723
  • Jilin City, Changchun, China|43.84652,126.5608
  • Hunan, Changsha, China|32.92741,120.18021
  • Sichuan, Chengdu, China|35.1221,105.48032
  • Chongqing, Chongqing Municipality, China|29.56026,106.55771

Key Eligibility Criteria

  • Histologically or cytologically confirmed locally advanced (stage IIIB/IIIC) NSCLC that is not amenable to radical surgery or radical radiochemothe…
  • Subjects with unresectable locally advanced or metastatic or recurrent NSCLC who have failed first-line treatment with PD-1/PD-L1 inhibitors combin…
  • Subjects must have at least one measurable lesion according to RECIST v1.1.

For full eligibility, visit ClinicalTrials.gov.

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