Ying Cheng
Changchun, China
NCT Number: NCT04012606
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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Notify Me18 year and older
All sexes
Interventional
Phase 3
Changchun, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
TORIPALIMAB INJECTION(JS001 ) or Placebo combined with chemotherapy, 240mg/6ml/vial, Q3W,up to 2 years of treatment.
Time frame: Approximately 2 years
Progression free survival (PFS) evaluated by investigators according to the response evaluation criteria in solid tumors (RECIST 1.1)
Time frame: Approximately 2.8 years
Overall suvival (OS)
Time frame: Approximately 2 years
PFS evaluated by the Blinded Individual Review Committee (BIRC) based on RECIST1.1 criteria;
Time frame: Approximately 2 years
Objective response rate (ORR) evaluated by investigators and BIRC based on RECIST1.1;
Time frame: Approximately 2 years
Duration of response (DOR) evaluated by investigators and BIRC based on RECIST1.1;
Time frame: Approximately 2 years
Disease control rate (DCR) evaluated by investigators and BIRC based on RECIST1.1;
Time frame: Approximately 2 years
Time to response (TTR) evaluated by investigators and BIRC based on RECIST1.1;
Time frame: Approximately 2 years
OS rates at 1 and 2 years
Time frame: Approximately 2 years
Adverse events (AEs) ; serious adverse events (SAEs); abnormal value of Lab test according to NCI-CTCAE V5.0
Time frame: Approximately 1year
PFS rates at 6-month(inestigators and BICR) and at 1-year
Shanghai Junshi Bioscience Co., Ltd.
Other
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
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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