Vaginal dryness

  • sponsor
    Teva Pharmaceuticals, USA
Updated on 25 March 2021


Vaginal dryness


A randomized, double-blinded, placebo-controlled, parallel design, multiple site study to evaluate the therapeutic equivalence of Estradiol vaginal cream USP, 0.01% (TEVA Pharmaceuticals, USA) to Estrace Estradiol vaginal cream, USP, 0.01% (Warner Chilcott) in treatment of atrophic vaginitis. There will be financial compensation for time and travel.

Condition Vaginal Atrophy
Clinical Study IdentifierTX147260
SponsorTeva Pharmaceuticals, USA
Last Modified on25 March 2021


Yes No Not Sure

Inclusion Criteria

Subject is 30-75 years old at screening
Subject is a postmenopausal woman
Last spontaneous period >12 months
Hysterectomy without oophorectomy
Bilateral oophorectomy
Report moderate to severe vaginal dryness
>40 years normal mammogram within the last nine months or one will be done for the purpose of the study
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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