Last update 17 May 2025

SHR-1702

Overview

Basic Info

Drug Type
Monoclonal antibody
Synonyms
SHR 1702
Target
TIM3
Action
inhibitors
Mechanism
TIM3 inhibitors(Hepatitis A virus cellular receptor 2 inhibitors)
Therapeutic Areas
NeoplasmsHemic and Lymphatic Diseases
Active Indication-
Inactive Indication
Advanced Malignant Solid NeoplasmMyelodysplastic SyndromesRefractory acute myeloid leukemia
Originator Organization
Jiangsu Hengrui Pharmaceuticals Co., Ltd.Jiangsu Hengrui Pharmaceuticals Co., Ltd.
Active Organization-
Inactive Organization
Jiangsu Hengrui Pharmaceuticals Co., Ltd.Jiangsu Hengrui Pharmaceuticals Co., Ltd.
License Organization-
Drug Highest PhaseDiscontinuedPhase 1
First Approval Date-
Regulation-
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Related

2
Clinical Trials associated with SHR-1702
NCT04443751
/ CompletedPhase 1
A Phase I, Multicenter, Open-label Study of SHR-1702 in Patients With Acute Myeloid Leukemia or Myelodysplastic Syndrome
NCT03871855
/ TerminatedPhase 1
A Study of SHR-1702 Alone or With Camrelizumab in Participants With Advanced Relapsed/Refractory Solid Tumors
100 Clinical Results associated with SHR-1702
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100 Translational Medicine associated with SHR-1702
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100 Patents (Medical) associated with SHR-1702
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100 Deals associated with SHR-1702
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Myelodysplastic SyndromesPhase 1
China
Jiangsu Hengrui Pharmaceuticals Co., Ltd.Jiangsu Hengrui Pharmaceuticals Co., Ltd.
10 Sep 2020
Refractory acute myeloid leukemiaPhase 1
China
Jiangsu Hengrui Pharmaceuticals Co., Ltd.Jiangsu Hengrui Pharmaceuticals Co., Ltd.
10 Sep 2020
Advanced Malignant Solid NeoplasmPhase 1
China
Jiangsu Hengrui Pharmaceuticals Co., Ltd.Jiangsu Hengrui Pharmaceuticals Co., Ltd.
28 Apr 2019
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Translational Medicine

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Deal

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Core Patent

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Clinical Trial

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Approval

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Biosimilar

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Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

Regulation

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