A Study of SHR-1316 and Fluzoparib（SHR-3162） in Small Cell Lung Cancer Patients

Phase 1

Completed

• Conditions: Small Cell Lung Cancer

• Registration Number: NCT04041011
• Lead Sponsor: Jiangsu HengRui Medicine Co., Ltd.

Brief Summary

The purpose of this study is to evaluate the safety and efficacy of SHR-1316 in combination with Fluzoparib（SHR-3162） in Small Cell Lung Cancer Patients

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2019-07-31
• Study First Submitted QC: 2019-07-31
• Study First Posted: 2019-08-01
• Study Start: 2019-09-17
• Primary Completion: 2021-04-23
• Study Completion: 2021-04-23
• Status Verified: 2022-06
• Last Update Submitted: 2022-06-16
• Last Update Posted: 2022-06-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 23

Inclusion Criteria

• Patients must be at least 18 years of age.
• Histologically or cytologically confirmed SCLC.
• Failed at least one prior line of platinum-based chemotherapy.
• Patients must have measurable disease as defined by RECIST v1.1.
• ECOG 0-1.
• Adequate hematologic and organ function
• Signed inform consent form

Exclusion Criteria

• Active or untreated central nervous system (CNS) metastases
• Spinal cord compression not definitively treated with surgery and/or radiation .
• Leptomeningeal disease
• Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures
• Malignancies other than SCLC within 5 years prior to randomization
• History of autoimmune disease
• Positive test result for human immunodeficiency virus (HIV)
• Active hepatitis B or hepatitis C
• Severe infections
• Subjects with a condition requiring systemic treatment with either corticosteroids (>10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of first administration of study treatment.
• Significant cardiovascular disease
• Prior allogeneic bone marrow transplantation or solid organ transplant
• Treatment with systemic immunosuppressive medications prior to randomization
• Pregnant or lactating women
• History or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with the subject's participation for the full duration of the study, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Part 1: 2. RP2D: Recommended dose for phase II study	Up to approximately 24 months.
Part 1: 1.Number of Participants with AEs and SAEs	Up to approximately 24 months.
Part 2: 1. ORR: Percentage of Participants With a CR or PR	Up to approximately 24 months.

Secondary Outcome Measures

Name	Time	Method
Part 1: 1. ORR: Percentage of Participants With a CR or PR	Up to approximately 24 months.
Part 2: 3. DCR: Percentage of participants in the analysis population who have a CR, PR or SD per RECIST 1.1.	Up to approximately 24 months.
Part 2: 1.Number of Participants with AEs and SAEs	Up to approximately 24 months.
Part 2: 4. PFS: PFS is defined as the time from randomization to the first documented disease progression per RECIST 1.1 based on blinded independent central review or death due to any cause, whichever occurs first.	Up to approximately 24 months.
Part 2: 2.DoR: Percentage of Participants With a CR or PR	Up to approximately 24 months.
Part 2: 5. OS: Baseline until death from any cause	Up to approximately 24 months.

Trial Locations

Locations (1)

Cancer Hospital of the University of Chinese Academy of Sciences Zhejiang Cancer Hospital; 🇨🇳 Hangzhou, Zhejiang, China