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The safety, tolerability and pharmacokinetics of a single intravenous infusion of 10, 40 and 80 ?g/kg XG-102 administered to healthy male volunteers in a randomized, double blind, placebo controlled, dose escalating Phase I study, Sponsor protocol identif
Third-party funded project |
Project title |
The safety, tolerability and pharmacokinetics of a single intravenous
infusion of 10, 40 and 80 ?g/kg XG-102 administered to healthy male
volunteers in a randomized, double blind, placebo controlled, dose
escalating Phase I study,
Sponsor protocol identifying number: SDD-1002-024
CRO protocol identifying number: BCRU560-1 |
Principal Investigator(s) |
Prünte, Christian
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Organisation / Research unit |
Bereich Spezialfächer (Klinik) / Ophthalmologie USB |
Project start |
01.07.2011 |
Probable end |
31.10.2011 |
Status |
Completed |
Abstract |
Fördergeber: Convance Clinical Research, Unit AG, Lettenweg 118, CH-4123 Allschwil, Diese Studie war eine Auftragsarbeit, daher haben wir den Betrag von 19666 CHF erhalten.
(The safety, tolerability and pharmacokinetics of a single intravenous
infusion of 10, 40 and 80 ?g/kg XG-102 administered to healthy male
Keine Fördergelder von Basel!
volunteers in a randomized, double blind, placebo controlled, dose
escalating Phase I study,
Sponsor protocol identifying number: SDD-1002-024
CRO protocol identifying number: BCRU560-1) |
Financed by |
Other sources
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05/05/2024
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