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

Phase 3Not Yet RecruitingNCT06526624

Hansoh BioMedical R&D Company406 enrolled

Overview

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.

This is a randomized, controlled, open-label, multi-center, phase III clinical study to evaluate the efficacy and safety of HS-20093 versus active surveillance as consolidation therapy in participants with limited-stage small cell lung cancer (LS-SCLC) who have not progressed after receiving chemoradiotherapy (CRT). This study consists of an experimental arm and a control arm. The experimental arm will be administered HS-20093, and the control arm will only receive active surveillance. Efficacy and safety were assessed in both arms by follow-up analyses.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

406

Conditions

Limited-stage Small-cell Lung Cancer

Interventions

HS-20093DRUG

Subjects in experimental arm will be given HS-20093 intravenously at a dose of 8.0 mg/kg every 3 weeks, until disease progression or until other criteria for treatment discontinuation are met.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Have signed Informed Consent Form. 2. Males or females ≥18 years old. 3. Patients with limited-stage SCLC who are deemed unsuitable for surgery or decline surgery. 4. ECOG performance status of 0-1. 5. Patients who have received CRT and have not progressed. 6. Minimum life expectancy \> 12 weeks. 7. Males or Females should be using adequate contraceptive measures throughout the study. 8. Females must not be pregnant at screening or have evidence of non-childbearing potential. Exclusion Criteria: 1. Patients with mixed SCLC or NSCLC or sarcoma-like carcinoma, or large cell neuroendocrine carcinoma. 2. Patients with extensive-stage SCLC. 3. Disease progression during CRT or before randomization. 4. Received or are receiving the following treatments: 1. For LS-SCLC, prior treatment with or current use of other chemotherapy regimens other than platinum plus etoposide 2. Received any other anti-cancer treatment. 3. Previous or current treatment with B7-H3 target therapy. 4. Traditional Chinese medicine indicated for tumors within 2 weeks prior to the first dose of study drug. 5. Major surgery within 4 weeks prior to the first dose of study drug. 5. Interstitial lung disease (ILD)/non-infectious pneumonitis. 6. History of other primary malignancies. 7. Inadequate bone marrow reserve or organ functions. 8. Severe, uncontrolled or active cardiovascular disorders. 9. Severe or uncontrolled diabetes. 10. Serious or poorly controlled hypertension. 11. Severe bleeding symptoms or bleeding tendencies within 1 month prior to randomization. 12. Severe arteriovenous thrombosis occurred within 3 months prior to randomization. 13. Serious infection within 4 weeks prior to randomization. 14. Presence of Grade ≥ 2 toxicities due to prior anti-tumor therapy. 15. Having serious neurological or mental disorders. 16. History of hypersensitivity to any component of HS-200093 or its similar drugs. 17. Participants with any condition that compromises the safety of the participant or interferes with the assessment of the study, as judged by the investigator.

Outcomes

Primary Outcomes

Progression-free survival (PFS) According to RECIST v1.1 by Independent Review Committee (IRC)

To assess the efficacy of HS-20093 vs active surveillance in terms of PFS. PFS is defined as the time from randomization until the date of objective disease progression or death, whichever occurred first, based on IRC using RECIST v1.1.

Time frame: Approximately 6 years

Overall survival (OS)

To assess the efficacy of HS-20093 vs active surveillance in terms of OS. Overall Survival is defined as the time from the date of randomization to the date of participant's death due to any cause.

Time frame: Approximately 6 years

Secondary Outcomes

PFS at 12 Months (PFS12) or 18 Months (PFS18) According to RECIST v1.1 by IRC

PFS12 and PFS18 are defined as the progression-free survival at 12 months and 18 months from the date of randomization, respectively, based on IRC using RECIST v1.1.

Time frame: Approximately 6 years.

ORR According to RECIST v1.1 by IRC

ORR is defined as the percentage of participants with BOR of CR or PR per RECIST v1.1

Time frame: From the date of randomization until the date of disease progression or withdrawal from study, up to approximately 6 years.

DCR According to RECIST v1.1 by IRC

DCR is deﬁned as the percentage of patients who have a best overall response (confirmed CR, PR, or stable disease)

Time frame: From the date of randomization until the date of disease progression or withdrawal from study, approximately 6 years.

DoR by IRC

DoR only applies to participants whose best overall response is CR or PR. The start date is the date of first documented response of CR or PR, and the end date is defined as the date of the first documented progression or death due to underlying disease.

Data from ClinicalTrials.gov

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