Last update 17 Jul 2025

XB-2202

Overview

Basic Info

Drug Type
Monoclonal antibody
Synonyms
antibody program(X-BODY / Jiangsu Hengrui), mAb program (age related macular degen), PDGF receptor beta targeted mAb(X-Body)
+ [3]
Target
mTOR
Action
inhibitors
Mechanism
mTOR inhibitors(Serine/threonine-protein kinase mTOR inhibitors)
Therapeutic Areas
NeoplasmsCongenital DisordersEye Diseases
Active Indication-
Inactive Indication
Dystrophy, MacularNeoplasms
Originator Organization
X-Body, Inc.X-Body, Inc.
Active Organization-
Inactive Organization
X-Body, Inc.X-Body, Inc.Jiangsu Hengrui Pharmaceuticals Co., Ltd.Jiangsu Hengrui Pharmaceuticals Co., Ltd.Juno Therapeutics, Inc.Juno Therapeutics, Inc.
License Organization-
Drug Highest PhasePendingDiscovery
First Approval Date-
Regulation-

Related

100 Clinical Results associated with XB-2202
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100 Translational Medicine associated with XB-2202
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100 Patents (Medical) associated with XB-2202
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100 Deals associated with XB-2202
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Dystrophy, MacularDiscovery
United States
Juno Therapeutics, Inc.Juno Therapeutics, Inc.
-
Dystrophy, MacularDiscovery
China
Jiangsu Hengrui Pharmaceuticals Co., Ltd.Jiangsu Hengrui Pharmaceuticals Co., Ltd.
-
Dystrophy, MacularDiscovery
Hong Kong
Jiangsu Hengrui Pharmaceuticals Co., Ltd.Jiangsu Hengrui Pharmaceuticals Co., Ltd.
-
Dystrophy, MacularDiscovery
Taiwan Province
Jiangsu Hengrui Pharmaceuticals Co., Ltd.Jiangsu Hengrui Pharmaceuticals Co., Ltd.
-
NeoplasmsDiscovery
United States
X-Body, Inc.X-Body, Inc.
-
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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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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