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Estradiol/DRSP (Angeliq, BAY86-4891)

ApprovedCompleted
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82
Hype Score

Development Stage

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

Postmenopause

Conditions

Postmenopause

Trial Timeline

Sep 1, 2005 → Dec 1, 2006

NCT ID
NCT00185328

About Estradiol/DRSP (Angeliq, BAY86-4891)

Estradiol/DRSP (Angeliq, BAY86-4891) is a approved stage product being developed by Bayer for Postmenopause. The current trial status is completed. This product is registered under clinical trial identifier NCT00185328. Target conditions include Postmenopause.

Hype Score Breakdown

Clinical
30
Activity
20
Company
7
Novelty
10
Community
12

Clinical Trials (1)

NCT IDPhaseStatus
NCT00185328ApprovedCompleted

Competing Products

16 competing products in Postmenopause

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Comparator: placebo + Comparator: EstraceMerckPhase 1
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bazedoxifene/conjugated estrogens combination tabletPfizerPhase 1
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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 + PlaceboPfizerPre-clinical
22
PremarinPfizerPre-clinical
22
Bazedoxifene and conjugated estrogensPfizerPhase 1
32
Premarin/MPA + Premarin/MPA + Provera 10 mgPfizerPhase 1
32
Bazedoxifene/conjugated estrogensPfizerPhase 1
32
PremarinPfizerPhase 1
32
bazedoxifene BZA-20PfizerPhase 3
76
Trimegestone + 17b EstradiolPfizerApproved
84
Premarin/MPA 0.45 mg/1.5 mgPfizerPhase 1
32
Conjugated Estrogen Cream (Premarin®)PfizerPre-clinical
22
0.25mg DRSP / 0.5mg E2 (BAY86-4891) + 0.5mg NETA / 1.0mg E2 (Activella)BayerPhase 3
74
E2/LNG oral (Wellnara, BAY86-5029)BayerPre-clinical
20
Drospirenone/17ß-estradiol (Angeliq, BAY86-4891) + Drospirenone/17ß-estradiol (Angeliq, BAY86-4891) + SH K 00641 C - Medroxyprogesterone acetate / conjugated equine (Prempro TM)BayerPhase 2
49
Tibolone + Estradiol + Estradiol + Medroxy Progesterone AcetateOrganonApproved
80

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