Last update 03 Apr 2026

SHR-9539

Overview

Basic Info

Drug Type
Trispecific T-cell engager (TriTE)
Synonyms
SHR-9539
Target
CD3
Action
stimulants
Mechanism
CD3 stimulants(T cell surface glycoprotein CD3 stimulants)
Therapeutic Areas
NeoplasmsImmune System DiseasesHemic and Lymphatic Diseases
Active Indication
Multiple Myeloma
Inactive Indication-
Originator Organization
Shanghai Hengrui Pharmaceutical Co., Ltd.Shanghai Hengrui Pharmaceutical Co., Ltd.Suzhou Suncadia Biopharmaceuticals Co., Ltd.Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Active Organization
Suzhou Suncadia Biopharmaceuticals Co., Ltd.Suzhou Suncadia Biopharmaceuticals Co., Ltd.Shanghai Hengrui Pharmaceutical Co., Ltd.Shanghai Hengrui Pharmaceutical Co., Ltd.
Inactive Organization-
License Organization-
Drug Highest PhasePhase 1
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with SHR-9539
NCT06484777
/ RecruitingPhase 1
An Open-label, Multi-center Phase I Clinical Study of the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy of SHR-9539 Injection in Patients With Multiple Myeloma
100 Clinical Results associated with SHR-9539
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100 Translational Medicine associated with SHR-9539
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100 Patents (Medical) associated with SHR-9539
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100 Deals associated with SHR-9539
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Multiple MyelomaPhase 1
China
Suzhou Suncadia Biopharmaceuticals Co., Ltd.Suzhou Suncadia Biopharmaceuticals Co., Ltd.
24 Jul 2024
Multiple MyelomaPhase 1
China
Shanghai Hengrui Pharmaceutical Co., Ltd.Shanghai Hengrui Pharmaceutical Co., Ltd.
24 Jul 2024
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
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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

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.
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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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