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

Primary Purpose

Small Cell Lung Cancer

Status
Active
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
Fluzoparib
temozolomide
SHR-1316
Sponsored by
Jiangsu HengRui Medicine Co., Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Small Cell Lung Cancer

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Subjects who have recurrent small cell lung cancer confirmed by histology or cytology.
  2. Failed one prior line of platinum-based chemotherapy.
  3. 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) ;
  4. Freshly acquired samples or archived specimens within 12 months before randomization must be provided.
  5. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
  6. Participant must have a life expectancy ≥ 12 weeks.

Exclusion Criteria:

  1. Active or untreated central nervous system (CNS) metastases.
  2. Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures.
  3. History of autoimmune disease.
  4. Positive test result for human immunodeficiency virus (HIV).
  5. Active hepatitis B or hepatitis C.
  6. Severe infections.
  7. 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.
  8. Significant cardiovascular disease.
  9. 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.

Sites / Locations

  • West China Hospital of Sichuan University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Experimental A (part 1) : Fluzoparib + temozolomide

Experimental B (part 2) : Fluzoparib + temozolomide + SHR-1316

Arm Description

Outcomes

Primary Outcome Measures

Phase Ⅰb: Number of Subjects Experienced Any Dose-Limiting Toxicity (DLT) over the DLT period.
Phase Ⅰb: Determination of Recommended Phase II dose (RP2D) of Escalating Dose of Fluzoparib and temozolomide with or without SHR-1316.
Phase Ⅱ: Progression Free Survival (PFS) at four months.
Phase Ⅱ: Progression Free Survival (PFS) as Assessed by the Investigator according to RECIST v1.1.
Progression Free Survival, defined as the time from randomization to first assessment of disease progression or death, whichever is earlier.

Secondary Outcome Measures

Objective Response Rate
Objective Response Rate, determined using RECIST v1.1 criteria, defined as best overall response (complete or partial response) across all assessment time points.
Duration of Response
Duration of Response, determined using RECIST v1.1 criteria.
Disease Control Rate
Disease Control Rate, determined using RECIST v1.1 criteria.
Time to Response
Time to Response, defined as the time from randomization to PR or CR.
Overall survival and overall survival at 6 months, 9months and 12 months
Overall survival is the time interval from the date of randomization to death due to any reason or lost of follow-up.

Full Information

First Posted
May 7, 2020
Last Updated
February 9, 2023
Sponsor
Jiangsu HengRui Medicine Co., Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT04400188
Brief Title
A Study of Fluzoparib (SHR-3162) and Temozolomide With or Without SHR-1316 in Treating Patients With Replapsed Small Cell Lung Cancer
Official 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
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 11, 2020 (Actual)
Primary Completion Date
January 15, 2022 (Actual)
Study Completion Date
June 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Jiangsu HengRui Medicine Co., Ltd.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Small Cell Lung Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Fluzoparib (SHR-3162) combined with temozolomide or Fluzoparib (SHR-3162) and temozolomide with SHR-1316
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental A (part 1) : Fluzoparib + temozolomide
Arm Type
Experimental
Arm Title
Experimental B (part 2) : Fluzoparib + temozolomide + SHR-1316
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Fluzoparib
Intervention Description
Given PO
Intervention Type
Drug
Intervention Name(s)
temozolomide
Intervention Description
Given PO
Intervention Type
Biological
Intervention Name(s)
SHR-1316
Intervention Description
Given injection
Primary Outcome Measure Information:
Title
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 )
Title
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
Title
Phase Ⅱ: Progression Free Survival (PFS) at four months.
Time Frame
Up to approximately 2 Years
Title
Phase Ⅱ: Progression Free Survival (PFS) as Assessed by the Investigator according to RECIST v1.1.
Description
Progression Free Survival, defined as the time from randomization to first assessment of disease progression or death, whichever is earlier.
Time Frame
Up to approximately 2 Years
Secondary Outcome Measure Information:
Title
Objective Response Rate
Description
Objective Response Rate, determined using RECIST v1.1 criteria, defined as best overall response (complete or partial response) across all assessment time points.
Time Frame
up to approximately 2 Years
Title
Duration of Response
Description
Duration of Response, determined using RECIST v1.1 criteria.
Time Frame
Up to approximately 2 Years
Title
Disease Control Rate
Description
Disease Control Rate, determined using RECIST v1.1 criteria.
Time Frame
Up to approximately 2 Years
Title
Time to Response
Description
Time to Response, defined as the time from randomization to PR or CR.
Time Frame
Up to approximately 2 Years
Title
Overall survival and overall survival at 6 months, 9months and 12 months
Description
Overall survival is the time interval from the date of randomization to death due to any reason or lost of follow-up.
Time Frame
Up to approximately 1 Year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
You Lu, MD
Organizational Affiliation
West China Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
West China Hospital of Sichuan University
City
Chengdu
State/Province
Sichuan
ZIP/Postal Code
610015
Country
China

12. IPD Sharing Statement

Learn more about this trial

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

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