Last update 23 Jan 2025

10a(Stanford University)

Overview

Basic Info

Drug Type
Proteolysis-targeting chimeras (PROTAC)
Synonyms-
Target
PDCD2
Mechanism
PDCD2 inhibitors(programmed cell death 2 inhibitors)
Therapeutic Areas
Neoplasms
Active Indication
Neoplasms
Inactive Indication-
Originator Organization
Stanford UniversityStanford UniversityDana-Farber Cancer Institute, Inc.Dana-Farber Cancer Institute, Inc.
Active Organization
Stanford UniversityStanford UniversityDana-Farber Cancer Institute, Inc.Dana-Farber Cancer Institute, Inc.
Inactive Organization-
Drug Highest PhasePreclinical
First Approval Date-
Regulation-

Structure/Sequence

Molecular FormulaC46H43F3N6O7
InChIKeyVWGOZKTYUULSHB-XLYAUNJQSA-N
CAS Registry2971850-28-7

Related

100 Clinical Results associated with 10a(Stanford University)
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100 Translational Medicine associated with 10a(Stanford University)
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100 Patents (Medical) associated with 10a(Stanford University)
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100 Deals associated with 10a(Stanford University)
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
NeoplasmsPreclinical
US
Stanford UniversityStanford University
15 Sep 2023
NeoplasmsPreclinical
US
Dana-Farber Cancer Institute, Inc.Dana-Farber Cancer Institute, Inc.
15 Sep 2023
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Approval

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Regulation

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