Last update 08 May 2025

6MW3511

Overview

Basic Info

Drug Type
Monoclonal antibody
Synonyms
Target
PDL1 x TGF-β2
Action
inhibitors
Mechanism
PDL1 inhibitors(Programmed death-ligand 1 inhibitors), TGF-β2 inhibitors(Transforming growth factor beta 2 inhibitors)
Therapeutic Areas
Neoplasms
Active Indication
Advanced Malignant Solid Neoplasm
Inactive Indication-
Originator Organization
Mabwell (Shanghai) Bioscience Co., Ltd.Mabwell (Shanghai) Bioscience Co., Ltd.
Active Organization
Mabwell (Shanghai) Bioscience Co., Ltd.Mabwell (Shanghai) Bioscience Co., Ltd.
Inactive Organization-
License Organization-
Drug Highest PhasePhase 1/2
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with 6MW3511
CTR20222206
/ Not yet recruitingPhase 1/2
评估6MW3511在晚期实体瘤患者中的安全性、耐受性、药代动力学特征和初步疗效的Ⅰ/Ⅱ期临床研究
[Translation] A Phase I/II clinical study to evaluate the safety, tolerability, pharmacokinetic characteristics and preliminary efficacy of 6MW3511 in patients with advanced solid tumors
100 Clinical Results associated with 6MW3511
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100 Translational Medicine associated with 6MW3511
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100 Patents (Medical) associated with 6MW3511
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100 Deals associated with 6MW3511
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Advanced Malignant Solid NeoplasmPhase 2
China
Mabwell (Shanghai) Bioscience Co., Ltd.Mabwell (Shanghai) Bioscience Co., Ltd.
01 Sep 2022
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
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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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