Last reviewed · How we verify

NCT05837052

A Phase II Trial to Evaluate the Efficiency and Safety of Serplulimab Plus Chemotherapy as Conversion Therapy in NSCLC

Recruiting now Phase 2 Last updated 17 July 2023
What this trial tests

Phase 2 trial testing serplulimab plus chemotherapy as conversion treatment in Unresectable Lung Non-Small Cell Carcinoma in 49 participants. Currently enrolling.

Timeline
15 May 2023
Primary endpoint
30 June 2025
30 December 2026

Quick facts

Lead sponsorZhejiang University
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment49
Start date15 May 2023
Primary completion30 June 2025
Estimated completion30 December 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Zhejiang University

Who can join

Adults 18 to 75, any sex, with Unresectable Lung Non-Small Cell Carcinoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a phase II, single-arm study to evaluate the efficacy and safety of Serplulimab plus chemotherapy as conversion treatment in patients with stage IIIB-IVA oligometastatic non-small cell lung cancer.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Oligometastatic NSCLC: Current Perspectives and Future Challenges.
    Torresan S, Costa J, Zanchetta C, De Marchi L, et al · · 2025 · cited 6× · PMID 39996875 · DOI 10.3390/curroncol32020075

Verify or expand the search:

Other recruiting trials for Unresectable Lung Non-Small Cell Carcinoma

Currently open trials in the same condition.

Other Zhejiang University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05837052.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing