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Completed

NCT Number: NCT04012606

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

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).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Ying Cheng

Changchun, China

Who can participate

Healthy volunteers accepted: No

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

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

Treatment and study plan

TORIPALIMAB INJECTION(JS001 ) Carboplatin Cisplatin Etoposide Placebo

Drug

TORIPALIMAB INJECTION(JS001 ) or Placebo combined with chemotherapy, 240mg/6ml/vial, Q3W,up to 2 years of treatment.

Primary outcomes

  1. PFS (Progression Free Survival) by investigator

    Time frame: Approximately 2 years

    Progression free survival (PFS) evaluated by investigators according to the response evaluation criteria in solid tumors (RECIST 1.1)

  2. Overall suvival (OS)

    Time frame: Approximately 2.8 years

    Overall suvival (OS)

Secondary outcomes

  1. PFS (Progression Free Survival) per RECIST1.1 as Assessed by BIRC (Blinded Independent Review Board)

    Time frame: Approximately 2 years

    PFS evaluated by the Blinded Individual Review Committee (BIRC) based on RECIST1.1 criteria;

  2. ORR (Objective Response Rate)

    Time frame: Approximately 2 years

    Objective response rate (ORR) evaluated by investigators and BIRC based on RECIST1.1;

  3. DOR (Duration of Response)

    Time frame: Approximately 2 years

    Duration of response (DOR) evaluated by investigators and BIRC based on RECIST1.1;

  4. DCR (Disease of Response)

    Time frame: Approximately 2 years

    Disease control rate (DCR) evaluated by investigators and BIRC based on RECIST1.1;

  5. TTR (Time to Response)

    Time frame: Approximately 2 years

    Time to response (TTR) evaluated by investigators and BIRC based on RECIST1.1;

  6. OS (Overall Survival) rate

    Time frame: Approximately 2 years

    OS rates at 1 and 2 years

  7. Incidence of AEs/SAEs

    Time frame: Approximately 2 years

    Adverse events (AEs) ; serious adverse events (SAEs); abnormal value of Lab test according to NCI-CTCAE V5.0

  8. PFS (Progression Free Survival) Rate

    Time frame: Approximately 1year

    PFS rates at 6-month(inestigators and BICR) and at 1-year

Sponsors and collaborators

Lead sponsor

Shanghai Junshi Bioscience Co., Ltd.

Other

Registry information

Official study 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

Important dates

Study start
2019
Primary completion
2023
Study completion
2023
First posted
Jul 9, 2019
Registry last updated
Jan 16, 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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