Last update 21 Nov 2024

Teslexivir

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
+ [2]
Target
HPV E1 x HPV E2
Mechanism
HPV E1 inhibitors(HPV E1 inhibitors), HPV E2 inhibitors(HPV E2 inhibitors)
Therapeutic Areas
Infectious DiseasesSkin and Musculoskeletal DiseasesUrogenital Diseases
Active Indication
Condylomata Acuminata
Inactive Indication
Recurrent Respiratory Papillomatosis
Originator Organization
Aviragen TherapeuticsAviragen Therapeutics
Active Organization
Aviragen TherapeuticsAviragen Therapeutics
Inactive Organization
Vaxart, Inc.Vaxart, Inc.Anaconda Pharma SASUAnaconda Pharma SASU
Drug Highest PhasePhase 2
First Approval Date-
Regulation-
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Structure

Molecular FormulaC35H36BrN3O4
InChIKeyIYWCUQWSZXLRNG-UHFFFAOYSA-N
CAS Registry1075798-37-6

Related

2
Clinical Trials associated with Teslexivir
NCT02724254 / CompletedPhase 2
A Double-blind Placebo Controlled, Randomized, Phase II Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of Twice Daily Topical Applications of AP611074 5% Gel for up to 16 Weeks in Condyloma Patients
NCT01532102 / CompletedPhase 1/2
A Double-blind, Placebo Controlled, Randomized, Phase IIa Study to Assess the Safety, Tolerability, Efficacy, and Pharmacokinetics of Repeated Topical Applications Over 42 Days of AP611074 5% Gel in Condyloma Patients
100 Clinical Results associated with Teslexivir
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100 Translational Medicine associated with Teslexivir
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100 Patents (Medical) associated with Teslexivir
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100 Deals associated with Teslexivir
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Condylomata AcuminataPhase 2-
Aviragen TherapeuticsAviragen Therapeutics
-
Recurrent Respiratory PapillomatosisPreclinical
US
Vaxart, Inc.Vaxart, Inc.
-
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Clinical Trial

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Approval

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Regulation

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