Ozmosi | MDT-10013 Drug Profile
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MDT-10013

Alternative Names: mdt-10013, mdt10013, mdt 10013
Clinical Status: Inactive
Latest Update: 2017-10-13
Latest Update Note: Clinical Trial Update

Product Description

in the Treatment of Acute Postoperative Pain Following Total Knee Arthroplasty

Mechanisms of Action: Unknown

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: N/A

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: PaceMate
Company Location: Eastern America
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Pain, Postoperative

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT02263222

P13-02

P2

Withdrawn

Pain, Postoperative

2016-06-01

2019-03-20

NCT02077140

P13-01

P2

Completed

Pain, Postoperative

2015-11-01

2019-03-20

Treatments

Recent News Events

Date

Type

Title