Cancer Hospital of the University of Chinese Academy of Sciences Zhejiang Cancer Hospital
Hangzhou, Zhejiang, 310005, China
NCT Number: NCT04041011
The purpose of this study is to evaluate the safety and efficacy of SHR-1316 in combination with Fluzoparib(SHR-3162) in Small Cell Lung Cancer Patients
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Notify Me18 year–70 year
All sexes
Interventional
Phase 1
Hangzhou, Zhejiang, 310005, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
1.Drug: Fluzoparib capsule will be given orally. Drug: SHR-1316 given intravenously (IV).
2.Drug: Fluzoparib capsule will be given orally. Drug: SHR-1316 given intravenously (IV).
3.Drug: Fluzoparib capsule will be given orally. Drug: SHR-1316 given intravenously (IV).
Time frame: Up to approximately 24 months.
Time frame: Up to approximately 24 months.
Time frame: Up to approximately 24 months.
Time frame: Up to approximately 24 months.
Time frame: Up to approximately 24 months.
Time frame: Up to approximately 24 months.
Time frame: Up to approximately 24 months.
Time frame: Up to approximately 24 months.
Time frame: Up to approximately 24 months.
Jiangsu HengRui Medicine Co., Ltd.
Industry
A Phase Ib Study of SHR-1316 in Combination With Fluzoparib(SHR-3162) in Small Cell Lung Cancer Patients
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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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