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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
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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