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Toripalimab in Combination With Platinum Plus Etoposidein Patients With Extensive-Stage Small Cell Lung Cancer

Primary Purpose

Small Cell Lung Cancer

Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
TORIPALIMAB INJECTION(JS001 ) Carboplatin Cisplatin Etoposide Placebo
Sponsored by
Shanghai Junshi Bioscience 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 - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. ≥18 years , male or female;
  2. Histologically or cytologically confirmed ES-SCLC (per the Veterans Administration Lung Study Group (VALG) staging system
  3. ECOG PS 0~1;
  4. No prior treatment or immunocheckpoint inhibitors for ES-SCLC;
  5. Treatment-free for at least 6 months since last chemo/radiotherapy, among those treated (with curative intent) with prior chemo/radiotherapy for limited-stage SCLC;
  6. Patients with asymptomatic brain metastases who have received previous treatment
  7. Has provided tumor tissue samples
  8. Estimated survival time ≥8 weeks;
  9. There is at least one measurable lesion that conforms to RECIST criteria v1.1.For lesions that have received previous radiation therapy, the lesion can only be included in the measurable lesion if the disease progression is clear after radiotherapy and the lesion is not the only measurable lesion.
  10. Before the first dose of the study drug, it should have appropriate organ function, and the laboratory test value should meet the protocol.
  11. Has adequate hematologic and end organ function

Exclusion Criteria:

  1. Prior systemtic treatment for ES-SCLC;
  2. Prior treatment with any CD137 agnist or immunocheckpoint inhibitors.
  3. Subjects with active or untreated central nervous system (CNS) tumor metastasis;
  4. Spinal cord compression not definitively treated with surgery and/or radiation or previously diagnosed and treated spinal cord compression without evidence that disease has been clinically stable for ≥ 1 week prior to randomization
  5. Cancerous meningitis;
  6. Uncontrolled or symptomatic hypercalcemia;
  7. Other malignant tumors within 5 years prior to the first dose of study treatment
  8. Subjects with any active, known or suspected autoimmune disease;
  9. History of idiopathic pulmonary fibrosis, drug-induced pneumonitis,or evidence of active pneumonitis .
  10. Subjects who received major surgery within 28 days prior to enrollment or were not fully recovered from prior surgery;
  11. Significant cardiovascular disease, such as New York Heart Assoc

Sites / Locations

  • Ying ChengRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

TORIPALIMAB

Chemotherapy

Arm Description

Outcomes

Primary Outcome Measures

PFS (Progression Free Survival) by investigator
Progression free survival (PFS) evaluated by investigators according to the response evaluation criteria in solid tumors (RECIST 1.1)
Overall suvival (OS)
Overall suvival (OS)

Secondary Outcome Measures

PFS (Progression Free Survival) per RECIST1.1 as Assessed by BIRC (Blinded Independent Review Board)
PFS evaluated by the Blinded Individual Review Committee (BIRC) based on RECIST1.1 criteria;
ORR (Objective Response Rate)
Objective response rate (ORR) evaluated by investigators and BIRC based on RECIST1.1;
DOR (Duration of Response)
Duration of response (DOR) evaluated by investigators and BIRC based on RECIST1.1;
DCR (Disease of Response)
Disease control rate (DCR) evaluated by investigators and BIRC based on RECIST1.1;
TTR (Time to Response)
Time to response (TTR) evaluated by investigators and BIRC based on RECIST1.1;
OS (Overall Survival) rate
OS rates at 1 and 2 years
Incidence of AEs/SAEs
Adverse events (AEs) ; serious adverse events (SAEs); abnormal value of Lab test according to NCI-CTCAE V5.0
PFS (Progression Free Survival) Rate
PFS rates at 6-month(inestigators and BICR) and at 1-year

Full Information

First Posted
July 5, 2019
Last Updated
September 28, 2020
Sponsor
Shanghai Junshi Bioscience Co., Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT04012606
Brief Title
Toripalimab in Combination With Platinum Plus Etoposidein Patients With Extensive-Stage Small Cell Lung Cancer
Official Title
A Phase III Randomized, Double-Blind, Placebo-controlled Study of Platinum(Cisplatin or Carboplatin) Plus Etoposide With or Without Toripalimab as First Line Therapy in Patients With ExtensiveStage Small Cell Lung Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Unknown status
Study Start Date
July 23, 2019 (Actual)
Primary Completion Date
July 6, 2021 (Anticipated)
Study Completion Date
June 18, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai Junshi Bioscience Co., Ltd.

4. Oversight

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

5. Study Description

Brief Summary
This is a phase III, multicenter, double-blinded, placebo-controlled study of platinum(Cisplatin or Carboplatin) plus etoposide with or without toripalimab as first Line therapy in patients with extensive stage small cell lung cancer. The purpose of this study is to evaluate the safety and efficacy of toriplimab in combination with platinum(Cisplatin or Carboplatin) plus etoposide in treatment naive extensive stage small cell lung cancer. Participants will receive asigned study treatment until progressive disease (PD) as assessed by the investigator using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1).

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 3
Interventional Study Model
Sequential Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
420 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
TORIPALIMAB
Arm Type
Experimental
Arm Title
Chemotherapy
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
TORIPALIMAB INJECTION(JS001 ) Carboplatin Cisplatin Etoposide Placebo
Intervention Description
TORIPALIMAB INJECTION(JS001 ) or Placebo combined with chemotherapy, 240mg/6ml/vial, Q3W,up to 2 years of treatment.
Primary Outcome Measure Information:
Title
PFS (Progression Free Survival) by investigator
Description
Progression free survival (PFS) evaluated by investigators according to the response evaluation criteria in solid tumors (RECIST 1.1)
Time Frame
Approximately 2 years
Title
Overall suvival (OS)
Description
Overall suvival (OS)
Time Frame
Approximately 2.8 years
Secondary Outcome Measure Information:
Title
PFS (Progression Free Survival) per RECIST1.1 as Assessed by BIRC (Blinded Independent Review Board)
Description
PFS evaluated by the Blinded Individual Review Committee (BIRC) based on RECIST1.1 criteria;
Time Frame
Approximately 2 years
Title
ORR (Objective Response Rate)
Description
Objective response rate (ORR) evaluated by investigators and BIRC based on RECIST1.1;
Time Frame
Approximately 2 years
Title
DOR (Duration of Response)
Description
Duration of response (DOR) evaluated by investigators and BIRC based on RECIST1.1;
Time Frame
Approximately 2 years
Title
DCR (Disease of Response)
Description
Disease control rate (DCR) evaluated by investigators and BIRC based on RECIST1.1;
Time Frame
Approximately 2 years
Title
TTR (Time to Response)
Description
Time to response (TTR) evaluated by investigators and BIRC based on RECIST1.1;
Time Frame
Approximately 2 years
Title
OS (Overall Survival) rate
Description
OS rates at 1 and 2 years
Time Frame
Approximately 2 years
Title
Incidence of AEs/SAEs
Description
Adverse events (AEs) ; serious adverse events (SAEs); abnormal value of Lab test according to NCI-CTCAE V5.0
Time Frame
Approximately 2 years
Title
PFS (Progression Free Survival) Rate
Description
PFS rates at 6-month(inestigators and BICR) and at 1-year
Time Frame
Approximately 1year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥18 years , male or female; Histologically or cytologically confirmed ES-SCLC (per the Veterans Administration Lung Study Group (VALG) staging system ECOG PS 0~1; No prior treatment or immunocheckpoint inhibitors for ES-SCLC; Treatment-free for at least 6 months since last chemo/radiotherapy, among those treated (with curative intent) with prior chemo/radiotherapy for limited-stage SCLC; Patients with asymptomatic brain metastases who have received previous treatment Has provided tumor tissue samples Estimated survival time ≥8 weeks; There is at least one measurable lesion that conforms to RECIST criteria v1.1.For lesions that have received previous radiation therapy, the lesion can only be included in the measurable lesion if the disease progression is clear after radiotherapy and the lesion is not the only measurable lesion. Before the first dose of the study drug, it should have appropriate organ function, and the laboratory test value should meet the protocol. Has adequate hematologic and end organ function Exclusion Criteria: Prior systemtic treatment for ES-SCLC; Prior treatment with any CD137 agnist or immunocheckpoint inhibitors. Subjects with active or untreated central nervous system (CNS) tumor metastasis; Spinal cord compression not definitively treated with surgery and/or radiation or previously diagnosed and treated spinal cord compression without evidence that disease has been clinically stable for ≥ 1 week prior to randomization Cancerous meningitis; Uncontrolled or symptomatic hypercalcemia; Other malignant tumors within 5 years prior to the first dose of study treatment Subjects with any active, known or suspected autoimmune disease; History of idiopathic pulmonary fibrosis, drug-induced pneumonitis,or evidence of active pneumonitis . Subjects who received major surgery within 28 days prior to enrollment or were not fully recovered from prior surgery; Significant cardiovascular disease, such as New York Heart Assoc
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ying Cheng, prof
Phone
+86431-8587-1902
Email
jl.cheng@163.com
Facility Information:
Facility Name
Ying Cheng
City
Chang chun
Country
China
Individual Site Status
Recruiting

12. IPD Sharing Statement

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Toripalimab in Combination With Platinum Plus Etoposidein Patients With Extensive-Stage Small Cell Lung Cancer

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