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Completed

NCT Number: NCT04400188

A Study of Fluzoparib (SHR-3162) and Temozolomide With or Without SHR-1316 in Treating Patients With Replapsed Small Cell Lung Cancer

This research study is a multicentre phase Ⅰb/Ⅱ Study to evaluate the efficacy and safety of the combination of Fluzoparib (SHR-3162) and temozolomide with or without SHR-1316 in small cell lung cancer

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

West China Hospital of Sichuan University

Chengdu, Sichuan, 610015, China

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Subjects who have recurrent small cell lung cancer confirmed by histology or cytology.
  • Failed one prior line of platinum-based chemotherapy.
  • Subjects must have measurable disease, at least one lesion, by Computed Tomography (CT) or Magnetic Resonance Imaging (MRI) per RECIST 1.1 criteria (within 28 days prior to administration of study treatment) ;
  • Freshly acquired samples or archived specimens within 12 months before randomization must be provided.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
  • Participant must have a life expectancy ≥ 12 weeks.

Exclusion criteria

  • Active or untreated central nervous system (CNS) metastases.
  • Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures.
  • 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.
  • 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

Fluzoparib

Drug

Given PO

Temozolomide

Drug

Given PO

SHR-1316

Biological

Given injection

Primary outcomes

  1. Phase Ⅰb: Number of Subjects Experienced Any Dose-Limiting Toxicity (DLT) over the DLT period.

    Time frame: At the end of Cycle1 (each cycle is 21 days )

  2. Phase Ⅰb: Determination of Recommended Phase II dose (RP2D) of Escalating Dose of Fluzoparib and temozolomide with or without SHR-1316.

    Time frame: Up to approximately 2 Years

  3. Phase Ⅱ: Progression Free Survival (PFS) at four months.

    Time frame: Up to approximately 2 Years

  4. Phase Ⅱ: Progression Free Survival (PFS) as Assessed by the Investigator according to RECIST v1.1.

    Time frame: Up to approximately 2 Years

    Progression Free Survival, defined as the time from randomization to first assessment of disease progression or death, whichever is earlier.

Secondary outcomes

  1. Objective Response Rate

    Time frame: up to approximately 2 Years

    Objective Response Rate, determined using RECIST v1.1 criteria, defined as best overall response (complete or partial response) across all assessment time points.

  2. Duration of Response

    Time frame: Up to approximately 2 Years

    Duration of Response, determined using RECIST v1.1 criteria.

  3. Disease Control Rate

    Time frame: Up to approximately 2 Years

    Disease Control Rate, determined using RECIST v1.1 criteria.

  4. Time to Response

    Time frame: Up to approximately 2 Years

    Time to Response, defined as the time from randomization to PR or CR.

  5. Overall survival and overall survival at 6 months, 9months and 12 months

    Time frame: Up to approximately 1 Year

    Overall survival is the time interval from the date of randomization to death due to any reason or lost of follow-up.

Sponsors and collaborators

Lead sponsor

Jiangsu HengRui Medicine Co., Ltd.

Industry

Registry information

Official study title

A Phase Ⅰb/Ⅱ Study of Fluzoparib (SHR-3162) and Temozolomide With or Without SHR-1316 in Treating Patients With Replapsed Small Cell Lung Cancer

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
May 22, 2020
Registry last updated
Jun 29, 2025

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.

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