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Safety, Tolerability and Pharmacokinetics of S 95010 After Single Escalating Intravenous Doses in Young Healthy Male Subjects. A Randomised, Doubleblind, Placebo-controlled, Monocentre, First-In-Human Study

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Study Phase

Phase 1

Therapeutic Area

Cardiovascular Diseases

IndicationHeart failure
SponsorInstitut de Recherches Internationales Servier (I.R.I.S)
Active substance/
Medical device


Active Substance CodeS095010
Protocol CodeCL1-95010-001
EudraCT Code2017-004180-12
NCT CodeNCT03494712

Documents and links

Results summary READ MORE

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