Last update 08 May 2025

AZD-2315

Overview

Basic Info

Drug Type
Synthetic peptide
Synonyms
Target-
Action-
Mechanism
Immunosuppressants
Therapeutic Areas
Immune System DiseasesSkin and Musculoskeletal Diseases
Active Indication-
Inactive Indication
Rheumatoid Arthritis
Originator Organization
AstraZeneca PLCAstraZeneca PLC
Active Organization-
Inactive Organization
AstraZeneca Pharmaceuticals Co. Ltd.AstraZeneca Pharmaceuticals Co. Ltd.AstraZeneca PLCAstraZeneca PLC
License Organization-
Drug Highest PhaseDiscontinuedPhase 1
First Approval Date-
Regulation-
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Structure/Sequence

Molecular FormulaC50H76N16O10
InChIKeyUIYUIDKHXAZHSB-KEWIHSFBSA-N
CAS Registry195607-36-4

Related

100 Clinical Results associated with AZD-2315
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100 Translational Medicine associated with AZD-2315
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100 Patents (Medical) associated with AZD-2315
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1
Literatures (Medical) associated with AZD-2315
Synthesis of isotopomers of the MHC II antagonist AZD2315
100 Deals associated with AZD-2315
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Rheumatoid ArthritisPhase 1-
AstraZeneca Pharmaceuticals Co. Ltd.AstraZeneca Pharmaceuticals Co. Ltd.
-
Rheumatoid ArthritisPhase 1
United Kingdom
AstraZeneca PLCAstraZeneca PLC
-
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

No Data

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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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