Status:
COMPLETED
Comparability DE vs CD-CHO1
Lead Sponsor:
Bristol-Myers Squibb
Conditions:
Healthy Subjects
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
Study to Compare the Pharmacokinetics of CD-CHO1 Process BMS-188667 to DE Process BMS-188667 in Healthy Subjects
Eligibility Criteria
Inclusion
- Signed consent form
- Healthy subjects as determined by good health as determined by no clinically significant deviation from normal in medical history, physical examination, ECGs and clinical laboratory determinations.
- Body weight for all subjects will be \<- 100 kg.
- body Mass Index (BMI) of 18-30 kg/m2 inclusive; BMI = weight (kg)/\[height (m)\]2
- Men and women (not nursing, not prgnant), who are at least 18 years of age. Women of childbearing potential (WOCBP) must be using an adequate method of contraception to avoid pregnancy throughout the study for at least 4 weeks before and for up to 10 weeks after the infusion of BMS-188667 in such a manner that the risk of pregnancy is minimized.
Exclusion
- WOCBP and males who are unwilling or unable to use an acceptable method to avoid pregnancy for up to 10 weeks after he infusion of BMS-1886678. WOCBP must also be using an acceptable method of contraception for at least 1 month before dosing.
- Women who are pregnant ore breast-feeding.
- Women with positive pregnanacy tes on enrollment or prior to study drug administration.
- History or current evidence of any signiicant acute or chroinic medical illness
Key Trial Info
Start Date :
September 1 2002
Trial Type :
INTERVENTIONAL
End Date :
December 1 2002
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT00277199
Start Date
September 1 2002
End Date
December 1 2002
Last Update
April 13 2011
Active Locations (1)
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1
Inveresk Clinical Research
Edinburgh, United Kingdom