SDTM001 Injection as Adjuvant Therapy for NSCLC Patients After Radical Surgical Resection

The goal of this clinical trial is to evaluate the safety profile and tolerability of SDT-M001 injection in NSCLC patients with driver-gene-negative and negative PD-L1 expression after radical surgical resection; to determine the recommended Phase II dose (RP2D).

Trial Details

NCT ID
NCT07096882
Phase
PHASE1
Sponsor
Cytocraft Biopharmaceutical Co., Ltd.
Status
RECRUITING
Cancer Type
Non-Small Cell (NSCLC) Lung Cancer
Interventions
  • SDT-M001 injection
Locations (sample)
  • Chengdu, Sichuan, China|30.66667,104.06667

Key Eligibility Criteria

  • All participants must be informed of the trial before any examinations stipulated in this trial are initiated, voluntarily sign the written informe…
  • Age ranges from 18 to 70 years old (including threshold), regardless of gender.
  • For participants diagnosed with primary NSCLC according to the standards of the "Chinese Medical Association guideline for clinical diagnosis and t…
  • There is no disease recurrence (including local recurrence) after radical surgical resection (R0) treatment, and the estimated time of apheresis is…

For full eligibility, visit ClinicalTrials.gov.

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