MK-6913 + 17-β estradiol + Placebo to MK-6913 + Placebo to 17-β estradiol + MK-6913 25 mg

Phase 2Terminated
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52
Hype Score

Development Stage

Pre-clinical
Phase 1
3
Phase 2
4
Phase 3
5
Approved
Indication / Disease

Moderate to Severe Vasomotor Symptoms in Postmenopausal

Conditions

Moderate to Severe Vasomotor Symptoms in Postmenopausal, Women

Trial Timeline

Dec 17, 2009 → Jul 30, 2010

About MK-6913 + 17-β estradiol + Placebo to MK-6913 + Placebo to 17-β estradiol + MK-6913 25 mg

MK-6913 + 17-β estradiol + Placebo to MK-6913 + Placebo to 17-β estradiol + MK-6913 25 mg is a phase 2 stage product being developed by Merck for Moderate to Severe Vasomotor Symptoms in Postmenopausal. The current trial status is terminated. This product is registered under clinical trial identifier NCT01015677. Target conditions include Moderate to Severe Vasomotor Symptoms in Postmenopausal, Women.

Hype Score Breakdown

Clinical
17
Activity
12
Company
10
Novelty
5
Community
5

Clinical Trials (1)

NCT IDPhaseStatus
NCT01015677Phase 2Terminated

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