Ikebukuro, Toshima-ku, 171-0014, Japan
NCT Number: NCT00505973
Study Evaluating the Safety and Tolerability of SCA-136 in Healthy Japanese Male Subjects
This study is being conducted to assess the safety and tolerability of ascending multiple oral doses of SCA-136 administered to healthy Japanese male subjects.
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Notify MeKey information
Age range
20 year–45 year
Sex eligibility
Male
Study type
Interventional
Phase
Phase 1
Primary location
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Healty Japanese men willing to use a medically acceptable form of contraception.
Exclusion criteria
- Any significant disease
- Positive urine drug screen
- Increased liver function tests
- Use of prescription drugs.
Treatment and study plan
SCA-136
DrugPrimary outcomes
-
Adverse events, safety laboratory results, vital signs, and ECGs will be used to monitor subject safety.
Sponsors and collaborators
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Registry information
Official study title
An Ascending Multiple Dose Study of the Safety, Pharmacokinetics, and Pharmacodynamics of SCA-136 Administered Orally to Healthy Japanese Male Subjects
Important dates
- Study start
- 2007
- Study completion
- 2007
- First posted
- Jul 25, 2007
- Registry last updated
- Dec 5, 2007
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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