Ozmosi | WO-3191 Drug Profile
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WO-3191

Alternative Names: wo-3191, wo3191, wo 3191
Clinical Status: Inactive
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: Unknown

Route of Administration: Vaginal

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Dr. August Wolff GmbH & Co. KG Arzneimittel
Company Location:
Company Founding Year: None
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT02687789

WOAF-11/2012

N/A

Completed

Vaginosis, Bacterial|Vaginal Diseases

2015-07-01

2019-03-20

Treatments

Recent News Events

Date

Type

Title