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Last Updated: October 23, 2020

DrugPatentWatch Database Preview

CLINICAL TRIALS PROFILE FOR PROMETRIUM

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All Clinical Trials for Prometrium

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00152438 Vasomotor Symptoms (VMS) Progesterone Study: Vasomotor Symptoms and Endothelial Function - Trial of Oral Micronized Progesterone Unknown status University of British Columbia Phase 2 2005-09-01 The primary purpose of this study is to determine the effects of a full dose (300 mg at hs) of oral micronized progesterone (OMP) on vasomotor symptoms [VMS] (hot flushes/night sweats), on forearm blood flow and on lipid levels and blood pressure in menopausal women without cardiovascular disease and with moderate to severe VMS. The hypotheses are that progesterone will improve hot flushes, increase endothelium-dependent forearm blood flow and will decrease blood pressure without change in lipid levels.
NCT00154180 Kronos Early Estrogen Prevention Study (KEEPS) Unknown status Albert Einstein College of Medicine of Yeshiva University Phase 4 2005-09-01 The study will examine the effects of estrogen and progesterone on the development of atherosclerosis in menopausal women when hormone treatment is initiated within 3 years of the menopausal transition.
NCT00154180 Kronos Early Estrogen Prevention Study (KEEPS) Unknown status Brigham and Women's Hospital Phase 4 2005-09-01 The study will examine the effects of estrogen and progesterone on the development of atherosclerosis in menopausal women when hormone treatment is initiated within 3 years of the menopausal transition.
NCT00154180 Kronos Early Estrogen Prevention Study (KEEPS) Unknown status Columbia University Phase 4 2005-09-01 The study will examine the effects of estrogen and progesterone on the development of atherosclerosis in menopausal women when hormone treatment is initiated within 3 years of the menopausal transition.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Prometrium

Condition Name

Condition Name for Prometrium
Intervention Trials
Menopause 3
Suicidal Ideation 3
Infertility 2
Preterm Birth 2
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Condition MeSH

Condition MeSH for Prometrium
Intervention Trials
Amenorrhea 4
Premature Birth 3
Suicidal Ideation 3
Infertility 2
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Clinical Trial Locations for Prometrium

Trials by Country

Trials by Country for Prometrium
Location Trials
United States 49
Canada 3
Australia 1
Italy 1
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Trials by US State

Trials by US State for Prometrium
Location Trials
California 6
North Carolina 5
Arizona 3
Washington 3
Massachusetts 3
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Clinical Trial Progress for Prometrium

Clinical Trial Phase

Clinical Trial Phase for Prometrium
Clinical Trial Phase Trials
Phase 4 8
Phase 3 4
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for Prometrium
Clinical Trial Phase Trials
Not yet recruiting 10
Recruiting 7
Completed 4
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Clinical Trial Sponsors for Prometrium

Sponsor Name

Sponsor Name for Prometrium
Sponsor Trials
National Institutes of Health (NIH) 3
University of North Carolina, Chapel Hill 3
National Institute of Mental Health (NIMH) 3
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Sponsor Type

Sponsor Type for Prometrium
Sponsor Trials
Other 41
NIH 9
Industry 2
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Serving leading biopharmaceutical companies globally:

McKesson
Boehringer Ingelheim
Moodys
Johnson and Johnson
Mallinckrodt
AstraZeneca

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