Last update 13 Jun 2025

STSA-1301

Overview

Basic Info

Drug Type
Monoclonal antibody
Synonyms
STSA 1301, STSA1301
Target
FcRn
Action
modulators
Mechanism
FcRn modulators(IgG receptor FcRn large subunit p51 modulators)
Therapeutic Areas
Immune System DiseasesHemic and Lymphatic Diseases
Active Indication
Purpura, Thrombocytopenic, Idiopathic
Inactive Indication-
Originator Organization
Staidson (Beijing) Biopharmaceuticals Co., Ltd.Staidson (Beijing) Biopharmaceuticals Co., Ltd.
Active Organization
Staidson (Beijing) Biopharmaceuticals Co., Ltd.Staidson (Beijing) Biopharmaceuticals Co., Ltd.
Inactive Organization-
License Organization-
Drug Highest PhasePhase 1/2
First Approval Date-
Regulation-
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Related

2
Clinical Trials associated with STSA-1301
NCT06929299
/ RecruitingPhase 1/2
A Phase Ib/II Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of STSA-1301 Subcutaneous Injection in Healthy Subjects and Patients With Immune Thrombocytopenia (ITP)
NCT06148389
/ CompletedPhase 1
A Randomized, Double-Blind, Placebo-Controlled, Single-ascending Dose, Phase Ia Study to Evaluate the Safety, Tolerability, Pharmacokinetic, Pharmacodynamics, and Immunogenicity of STSA-1301 Subcutaneous Injection in Healthy Subjects
100 Clinical Results associated with STSA-1301
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100 Translational Medicine associated with STSA-1301
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100 Patents (Medical) associated with STSA-1301
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100 Deals associated with STSA-1301
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Purpura, Thrombocytopenic, IdiopathicPhase 2
China
Staidson (Beijing) Biopharmaceuticals Co., Ltd.Staidson (Beijing) Biopharmaceuticals Co., Ltd.
12 May 2025
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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

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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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