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MK-1496

Alternative Names: mk-1496, mk1496, mk 1496
Latest Update: 2015-02-19
Latest Update Note: Clinical Trial Update

Product Description

Merck was developing mk-1496, an oral PLK1 Inhibitor for patients with locally advanced and/or metastatic solid tumors who have failed standard therapy or for whom no standard therapy exists. (Sourced from: https://clinicaltrials.gov/ct2/show/NCT00880568)

Mechanisms of Action: PLK1 Inhibitor

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Merck
Company Location: KENILWORTH NJ 07033
Company CEO: Robert M. Davis
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for MK-1496

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 1: Oncology Solid Tumor Unspecified

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

NCT00880568

P1

Completed

Oncology Solid Tumor Unspecified

2010-11-01

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