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An Ascending Multiple Dose Study of the Safety, Pharmacokinetics, and Pharmacodynamics of SCA-136 Administered Orally to Healthy Japanese and Non-Japanese Female Subjects
This study is being conducted to evaluate the safety and tolerability of ascending multiple oral doses of SCA-136 adminstered to healthy Japanese and non-Japanese female subjects.
Age
20 - 45 years
Sex
FEMALE
Healthy Volunteers
Yes
Glendale, California, United States
Start Date
April 1, 2007
Completion Date
September 1, 2007
Last Updated
December 5, 2007
64
ESTIMATED participants
SCA-136
DRUG
Lead Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
NCT07455929
NCT06740383
Data Source & Attribution
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