A Study of HS-20093 vs Active Surveillance in Limited-Stage Small Cell Lung Cancer

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorHansoh BioMedical R&D Company

About this trial

This study will evaluate the efficacy, safety and tolerability of HS-20093 compared with active surveillance as consolidation therapy after chemoradiotherapy in participants with limited-stage small cell lung cancer.

Eligibility criteria

Qualifiers

Have signed Informed Consent Form.

Males or females ≥18 years old.

Patients with limited-stage SCLC who are deemed unsuitable for surgery or decline surgery.

ECOG performance status of 0-1.

Disqualifiers

Patients with mixed SCLC or NSCLC or sarcoma-like carcinoma, or large cell neuroendocrine carcinoma.

Patients with extensive-stage SCLC.

Disease progression during CRT or before randomization.

For LS-SCLC, prior treatment with or current use of other chemotherapy regimens other than platinum plus etoposide

Trial design

Treatments tested in this trial

  • HS-20093

Treatment groups

406 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators