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

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Wyeth

Status and phase

Completed
Phase 1

Conditions

Atrophic Vaginitis

Treatments

Drug: Premarin® oral tablets
Drug: Premarin® Vaginal Cream

Study type

Interventional

Funder types

Industry

Identifiers

NCT00167921
0713S5-414

Details and patient eligibility

About

The purpose of this study is to characterize the systemic exposure and bioavailability at steady state of Premarin® Vaginal Cream compared with Premarin® oral tablets in postmenopausal women with atrophic vaginitis.

Sex

Female

Ages

45 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Generally healthy postmenopausal women.
  • Intact uterus.
  • Clinical diagnosis of moderate to severe atrophic vaginitis.

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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