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MDT-10013

Alternative Names: mdt-10013, mdt10013, mdt 10013
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: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Medtronic
Company Location: DUBLIN L2 2
Company CEO: Geoffrey S. Martha
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for MDT-10013

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 2: Pain, Postoperative

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success
P13-02

P2

Withdrawn

Pain, Postoperative

2016-06-01

P13-01

P2

Completed

Pain, Postoperative

2015-11-01

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