Premarin/MPA 0.45 mg/1.5 mg

Phase 1Completed

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Hype Score

Development Stage

✓

Pre-clinical

Phase 1

Phase 2

Phase 3

Approved

Indication / Disease

Postmenopause

Conditions

Postmenopause

Trial Timeline

May 1, 2007 → Aug 1, 2007

NCT ID

NCT00472927

About Premarin/MPA 0.45 mg/1.5 mg

Premarin/MPA 0.45 mg/1.5 mg is a phase 1 stage product being developed by Pfizer for Postmenopause. The current trial status is completed. This product is registered under clinical trial identifier NCT00472927. Target conditions include Postmenopause.

Hype Score Breakdown

Clinical

Activity

Company

Novelty

Community

Clinical Trials (1)

NCT ID	Phase	Status	Start	Completion	Indication
NCT00472927	Phase 1	Completed	May 1, 2007	Aug 1, 2007	Postmenopause

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16 competing products in Postmenopause

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Product	Company	Stage	Hype Score
Comparator: placebo + Comparator: Estrace	Merck	Phase 1	33
bazedoxifene/conjugated estrogens combination tablet	Pfizer	Phase 1	32
Bazedoxifene 10 mg/CE 0.625 mg + Bazedoxifene 20 mg/CE 0.625 mg + Bazedoxifene 40 mg/CE 0.625 mg + Bazedoxifene 10 mg/CE 0.45 mg + Bazedoxifene 20 mg/CE 0.45 mg + Bazedoxifene 40 mg/CE 0.45 mg + Raloxifene 60 mg + Placebo	Pfizer	Pre-clinical	22
Premarin	Pfizer	Pre-clinical	22
Bazedoxifene and conjugated estrogens	Pfizer	Phase 1	32
Premarin/MPA + Premarin/MPA + Provera 10 mg	Pfizer	Phase 1	32
Bazedoxifene/conjugated estrogens	Pfizer	Phase 1	32
Premarin	Pfizer	Phase 1	32
bazedoxifene BZA-20	Pfizer	Phase 3	76
Trimegestone + 17b Estradiol	Pfizer	Approved	84
Conjugated Estrogen Cream (Premarin®)	Pfizer	Pre-clinical	22
Estradiol/DRSP (Angeliq, BAY86-4891)	Bayer	Approved	82
0.25mg DRSP / 0.5mg E2 (BAY86-4891) + 0.5mg NETA / 1.0mg E2 (Activella)	Bayer	Phase 3	74
E2/LNG oral (Wellnara, BAY86-5029)	Bayer	Pre-clinical	20
Drospirenone/17ß-estradiol (Angeliq, BAY86-4891) + Drospirenone/17ß-estradiol (Angeliq, BAY86-4891) + SH K 00641 C - Medroxyprogesterone acetate / conjugated equine (Prempro TM)	Bayer	Phase 2	49
Tibolone + Estradiol + Estradiol + Medroxy Progesterone Acetate	Organon	Approved	80

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