Skip to main content
OpenTrials
Completed

NCT Number: NCT04041011

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

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

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Cancer Hospital of the University of Chinese Academy of Sciences Zhejiang Cancer Hospital

Hangzhou, Zhejiang, 310005, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

1.Experimental: A (Part 1): Fluzoparib and SHR -1316

Drug

1.Drug: Fluzoparib capsule will be given orally. Drug: SHR-1316 given intravenously (IV).

2.Experimental: B (Part 1): Fluzoparib and SHR -1316

Drug

2.Drug: Fluzoparib capsule will be given orally. Drug: SHR-1316 given intravenously (IV).

3.Experimental: C (Part 2): Fluzoparib and SHR -1316 Expansion

Drug

3.Drug: Fluzoparib capsule will be given orally. Drug: SHR-1316 given intravenously (IV).

Primary outcomes

  1. Part 1: 1.Number of Participants with AEs and SAEs

    Time frame: Up to approximately 24 months.

  2. Part 1: 2. RP2D: Recommended dose for phase II study

    Time frame: Up to approximately 24 months.

  3. Part 2: 1. ORR: Percentage of Participants With a CR or PR

    Time frame: Up to approximately 24 months.

Secondary outcomes

  1. Part 1: 1. ORR: Percentage of Participants With a CR or PR

    Time frame: Up to approximately 24 months.

  2. Part 2: 1.Number of Participants with AEs and SAEs

    Time frame: Up to approximately 24 months.

  3. Part 2: 2.DoR: Percentage of Participants With a CR or PR

    Time frame: Up to approximately 24 months.

  4. Part 2: 3. DCR: Percentage of participants in the analysis population who have a CR, PR or SD per RECIST 1.1.

    Time frame: Up to approximately 24 months.

  5. 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.

    Time frame: Up to approximately 24 months.

  6. Part 2: 5. OS: Baseline until death from any cause

    Time frame: Up to approximately 24 months.

Sponsors and collaborators

Lead sponsor

Jiangsu HengRui Medicine Co., Ltd.

Industry

Registry information

Official study title

A Phase Ib Study of SHR-1316 in Combination With Fluzoparib(SHR-3162) in Small Cell Lung Cancer Patients

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Aug 1, 2019
Registry last updated
Jun 21, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.