The objective of the study is to compare the efficacy, safety, and tolerance of a 50mg dose of a new antiprogestin, CDB 2914 with a 0.75mg dose of levonorgestrel as emergency contraception. This is a multicenter, randomized, double-blind phase II study intended to test a one dose regimen for emergency contraception against the current standard regimen. Subjects have two visits, enrollment and follow-up. If the subject has not had menses by her scheduled follow-up visit, she will be followed until she has her period, or it is determined that she is pregnant.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000056-39
Application #
6409163
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
1978-12-01
Project End
2003-11-30
Budget Start
Budget End
Support Year
39
Fiscal Year
2000
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Type
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
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