Study Comparing Four New Formulations for Premarin in Healthy Postmenopausal Women

A Study To Compare The Amount Of Premarin Components That Is Absorbed Into The Blood Of Japanese Healthy Postmenopausal Women Following Oral Administration Of Two Different Tablets Of Premarin Under Fast and Fed Conditions.

NCT01436513 ·Status: COMPLETED ·Phase: PHASE1

Medroxyprogesterone Acetate Injection 150 mg/1 mL in Postmenopausal Women

NCT00830414 ·Status: COMPLETED ·Phase: PHASE1

Study Comparing Premarin® Vaginal Cream Versus Premarin® Oral Tablets in Atrophic Vaginitis

NCT00167921 ·Status: COMPLETED ·Phase: PHASE1

Self Administration of Subcutaneous Depot Medroxyprogesterone Acetate

NCT00770887 ·Status: COMPLETED

A Pharmacokinetic Study to Evaluate the Bioequivalence of 2 Progesterone Vaginal Rings in Postmenopausal Women

NCT02092571 ·Status: COMPLETED ·Phase: PHASE1

A Long-Term Study to Evaluate the Safety of Asoprisnil and Estrogen Administration to Postmenopausal Women

NCT00152295 ·Status: COMPLETED ·Phase: PHASE2

Investigation of 2 Different Oral Formulations of Estradiol and Norethisterone in Healthy Women

NCT01596010 ·Status: COMPLETED ·Phase: PHASE1

Bioequivalence Study of Patches With Different Equilibration Profiles

NCT00775086 ·Status: COMPLETED ·Phase: PHASE1

A Bioequivalence Study Of Ethinylestradiol + Gestodene In Female And Healthy Volunteers.

NCT01260805 ·Status: COMPLETED ·Phase: PHASE1

Depo Provera Self-Administration Study: Putting a Patient-Centered Practice to the Test at Planned Parenthood

NCT02509767 ·Status: COMPLETED ·Phase: PHASE4

Study Evaluating Estradiol/Trimegestone in Vasomotor Symptoms (VMS) in Post-Menopausal Women.

NCT00195455 ·Status: COMPLETED ·Phase: PHASE4

Efficacy and Safety Study of an Oral Contraceptive in Healthy Females

NCT00206583 ·Status: COMPLETED ·Phase: PHASE3

Study of Safety and Efficacy of an Oral Contraceptive

NCT00391807 ·Status: COMPLETED ·Phase: PHASE3

Assessing the Effect of Multiple Doses of Zibotentan on the Pharmacokinetics of Single Doses of Combined Oral Contraceptives in Healthy Female Participants of Non-childbearing Potential.

NCT05505162 ·Status: COMPLETED ·Phase: PHASE1

Effects of Angeliq and Prempro on Blood Pressure and Sodium Sensitivity in Postmenopausal Women With Prehypertension

NCT00420342 ·Status: COMPLETED ·Phase: PHASE2

A Study to Investigate the Effects of BMS-986278 on Drospirenone and Ethinyl Estradiol Drug Levels in Healthy Female Participants

NCT05985590 ·Status: COMPLETED ·Phase: PHASE1

Mirena and Estrogen for Control of Perimenopause Symptoms and Ovulation Suppression

NCT01613131 ·Status: COMPLETED ·Phase: NA

Pharmacodynamics and Pharmacokinetics Study of Existing DMPA Contraceptive Methods

NCT02456584 ·Status: COMPLETED ·Phase: PHASE1

Clinical Study Investigating the Conversion of the Contraceptive Compound Norethisterone Within the Body Towards the Contraceptive Compound Ethinylestradiol

NCT02170038 ·Status: COMPLETED ·Phase: PHASE1

Estradiol/Norethindrone Acetate Tablets, 1/0.5 mg Under Fed Conditions

NCT01181726 ·Status: COMPLETED ·Phase: PHASE1

Micronized Progesterone Versus Norethisterone Acetate in Combination With Estrogen as Menopausal Hormone Therapy

NCT05586724 ·Status: RECRUITING ·Phase: PHASE3

Bioequivalence Study of the Oral Contraceptive (OC) Tablet Containing Norgestimate (NGM)/Ethinyl Estradiol (EE) With or Without Folic Acid in Healthy Women.

NCT00709644 ·Status: COMPLETED ·Phase: PHASE1

A Bioequivalence Study of Norgestimate /Ethinyl Estradiol (NGM/EE) Tablets Manufactured at 2 Different Facilities

NCT02127593 ·Status: COMPLETED ·Phase: PHASE1

To Compare SH T00658ID Over Ortho Tri-Cyclen Lo (US/Canada)

NCT00754065 ·Status: COMPLETED ·Phase: PHASE3

Comparative Bioavailability of Two Injectable Suspension Formulations of Medroxyprogesterone Acetate+Estradiol Cypionate

NCT03443089 ·Status: COMPLETED ·Phase: PHASE1