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WO-3191

Alternative Names: wo-3191, wo3191, wo 3191
Latest Update: 2016-02-22
Latest Update Note: Clinical Trial Update

Product Description

The vaginal suppository is used for the reduction and/or inhibition of vaginal biofilms that were shown to be related to recurrent bacterial vaginosis. (Sourced from: https://clinicaltrials.gov/ct2/show/study/NCT02687789)

Mechanisms of Action: Unknown

Novel Mechanism: No

Modality: N/A

Route of Administration: Vaginal

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Dr. August Wolff & KG Arzneimittel
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for WO-3191

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

WOAF-11/2012

N/A

Completed

Vaginosis, Bacterial|Vaginal Diseases

2015-07-01

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