Last update 31 May 2025

Recifercept

Overview

Basic Info

Drug Type
Fusion protein
Synonyms
Reciferecept, PF-07256472, TA-46
Target
Action
antagonists
Mechanism
FGFR3 antagonists(Fibroblast growth factor receptor 3 antagonists)
Active Indication-
Inactive Indication
Originator Organization
Active Organization-
Inactive Organization
License Organization-
Drug Highest PhaseDiscontinuedPhase 2
First Approval Date-
RegulationOrphan Drug (United States), Orphan Drug (European Union)
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Structure/Sequence

R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
AchondroplasiaPhase 2
United States
02 Dec 2020
AchondroplasiaPhase 2
Japan
02 Dec 2020
AchondroplasiaPhase 2
Australia
02 Dec 2020
AchondroplasiaPhase 2
Belgium
02 Dec 2020
AchondroplasiaPhase 2
Denmark
02 Dec 2020
AchondroplasiaPhase 2
Italy
02 Dec 2020
AchondroplasiaPhase 2
Portugal
02 Dec 2020
AchondroplasiaPhase 2
Spain
02 Dec 2020
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 2
60
(Recifercept 1 mg/kg QW)
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-
15 Feb 2024
(Recifercept 2 mg/kg BIW)
tdyavzoesc = wjchcpvuxo hogunsxmnf (byeuzlkboy, ollwanyakd - rlfukwqvps)
Phase 2
35
(Recifercept 1 Milligram Per Kilogram (mg/kg) Once Weekly)
fagaaiecfa = muxygijclw qlgqduanyd (ylzzuczqqb, epduocmint - yxjnlmgsgk)
-
08 Feb 2024
(Recifercept 2 mg/kg Twice Weekly)
fagaaiecfa = jcvqkwtail qlgqduanyd (ylzzuczqqb, ylqnnfwhmr - ohdifhrlaf)
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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.
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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