Last update 30 May 2025

Semaglutide/Dapagliflozin

Overview

Basic Info

Drug Type
Small molecule drug, Recombinant polypeptide
Synonyms-
Target
AMPK x GLP-1R x P-gp x SGLT2
Action
agonists, inhibitors
Mechanism
AMPK agonists(AMP活化蛋白激酶激动剂), GLP-1R agonists(Glucagon-like peptide 1 receptor agonists), P-gp inhibitors(P-glycoprotein 1 inhibitors)
Therapeutic Areas-
Active Indication-
Inactive Indication-
Originator Organization
Novo Nordisk A/SNovo Nordisk A/S
Active Organization-
Inactive Organization
Novo Nordisk A/SNovo Nordisk A/S
License Organization-
Drug Highest PhasePendingPhase 1
First Approval Date-
Regulation-
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Structure/Sequence

Molecular FormulaC24H35ClO9
InChIKeyGOADIQFWSVMMRJ-UPGAGZFNSA-N
CAS Registry960404-48-2

Related

1
Clinical Trials associated with Semaglutide/Dapagliflozin
NCT05429593
/ CompletedPhase 1
A Study Comparing Exposure of Semaglutide and Dapagliflozin Dosed Orally as Mono-components Versus in a Fixed-dose Combination
100 Clinical Results associated with Semaglutide/Dapagliflozin
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100 Translational Medicine associated with Semaglutide/Dapagliflozin
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100 Patents (Medical) associated with Semaglutide/Dapagliflozin
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100 Deals associated with Semaglutide/Dapagliflozin
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R&D Status

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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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