Last update 04 Dec 2025

PF-05230901

Overview

Basic Info

Drug Type
Monoclonal antibody
Synonyms
PF 5230901, PF-5230901
Target-
Action-
Mechanism-
Therapeutic Areas
Other Diseases
Active Indication-
Inactive Indication
Cachexia
Originator Organization
Pfizer Inc.Pfizer Inc.
Active Organization-
Inactive Organization
Pfizer Inc.Pfizer Inc.
License Organization-
Drug Highest PhaseDiscontinuedPhase 1
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with PF-05230901
NCT01262690
/ TerminatedPhase 1
A Phase 1 Ascending Single Dose Study To Evaluate The Safety, Tolerability, And Pharmacokinetics Of PF-05230901 Administered Subcutaneously To Healthy Subjects
100 Clinical Results associated with PF-05230901
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100 Translational Medicine associated with PF-05230901
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100 Patents (Medical) associated with PF-05230901
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100 Deals associated with PF-05230901
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
CachexiaPhase 1
United States
Pfizer Inc.Pfizer Inc.
01 Nov 2010
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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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