Last update 25 Jan 2025

UM-ERD-4001

Overview

Basic Info

Drug Type
Proteolysis-targeting chimeras (PROTAC)
Synonyms
UM ERD-4001, UMERD-4001, UM-ERD 4001
+ [1]
Target
ERα
Mechanism
ERα antagonists(Estrogen receptor alpha antagonists)
Therapeutic Areas
NeoplasmsSkin and Musculoskeletal Diseases
Active Indication
HER2-negative breast cancerHormone receptor positive breast cancerEstrogen receptor positive breast cancer
Inactive Indication-
Originator Organization
Proteovant Therapeutics, Inc.Proteovant Therapeutics, Inc.Startup
Active Organization
University of MichiganUniversity of MichiganProteovant Therapeutics, Inc.Proteovant Therapeutics, Inc.Startup
Inactive Organization-
Drug Highest PhasePreclinical
First Approval Date-
Regulation-

Related

100 Clinical Results associated with UM-ERD-4001
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100 Translational Medicine associated with UM-ERD-4001
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100 Patents (Medical) associated with UM-ERD-4001
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100 Deals associated with UM-ERD-4001
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
HER2-negative breast cancerPreclinical
US
University of MichiganUniversity of Michigan
09 Apr 2024
HER2-negative breast cancerPreclinical
US
Proteovant Therapeutics, Inc.Proteovant Therapeutics, Inc.Startup
09 Apr 2024
Hormone receptor positive breast cancerPreclinical
US
University of MichiganUniversity of Michigan
09 Apr 2024
Hormone receptor positive breast cancerPreclinical
US
Proteovant Therapeutics, Inc.Proteovant Therapeutics, Inc.Startup
09 Apr 2024
Estrogen receptor positive breast cancerPreclinical
US
Proteovant Therapeutics, Inc.Proteovant Therapeutics, Inc.Startup
22 Mar 2024
Estrogen receptor positive breast cancerPreclinical
US
University of MichiganUniversity of Michigan
22 Mar 2024
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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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