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Propiolactone

Alternative Names: propiolactone, betaprone, afluria quadrivalent, imovax rabies, flucelvax quadrivalent (multi-dose vial), flucelvax quadrivalent (pre-filled syringe)
Latest Update: 2024-03-20
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: DNA Adduct

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Topical,Nasal,Intramuscular

FDA Designation: None *

Approval Status: Approved

Approved Countries: Denmark | European Medicines Agency | Finland | Iceland | Ireland | Lithuania | Pakistan | Peru | Poland | Turkey | United States

Approved Indications: None

Known Adverse Events: None

Company: Seqirus
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Propiolactone

Countries in Clinic:

Active Clinical Trial Count: 2

Highest Development Phases

Phase 3: COVID-19|Influenza, Human

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

2021-003953-43

P3

Completed

Influenza, Human|COVID-19

2022-11-15

2016-004753-33

P3

Active, not recruiting

Influenza, Human

2021-02-22

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