Last update 08 May 2025

Limnetrelvir

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
Target
SARS-CoV-2 3CLpro
Action
inhibitors
Mechanism
SARS-CoV-2 3CLpro inhibitors(SARS-CoV-2-3C-like-proteinase inhibitors)
Therapeutic Areas
Infectious DiseasesRespiratory Diseases
Active Indication
COVID-19
Inactive Indication-
Originator Organization
AbbVie, Inc.AbbVie, Inc.
Active Organization
AbbVie, Inc.AbbVie, Inc.
Inactive Organization-
License Organization-
Drug Highest PhasePhase 1
First Approval Date-
Regulation-
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Structure/Sequence

Molecular FormulaC27H23F4N5O4
InChIKeyKPYQLMJUGSDJQX-MRXNPFEDSA-N
CAS Registry2923500-04-1

Related

6
Clinical Trials associated with Limnetrelvir
NCT06078202
/ WithdrawnPhase 1
Assessment of the Relative Bioavailability of Three Immediate-Release Tablet Formulations of ABBV-903 in Healthy Volunteers
NCT06009237
/ TerminatedPhase 1
A Study to Evaluate Pharmacokinetics, Safety, and Tolerability of ABBV-903 in Healthy Japanese and Han Chinese Subjects
NCT05995366
/ CompletedPhase 1
Mass Balance Study of [14C] ABBV-903 in Healthy Male Subjects Following Single Oral Dose Administration
100 Clinical Results associated with Limnetrelvir
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100 Translational Medicine associated with Limnetrelvir
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100 Patents (Medical) associated with Limnetrelvir
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100 Deals associated with Limnetrelvir
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
COVID-19Phase 1
United States
AbbVie, Inc.AbbVie, Inc.
03 Jan 2023
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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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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Regulation

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