A first time in man, phase I study to assess the safety, tolerability and pharmacokinetics of single ascending doses of CM3.1-AC100 in healthy male volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
56
Solution for sc injection, single ascending doses
Solution for sc injection
Parexel International GmbH
Berlin, State of Berlin, Germany
Safety measurements (Adverse events, ECG recordings, blood pressure, pulse, body temperature, laboratory variables,local tolerability, nausea questionnaire)
Time frame: Safety will be monitored continously and safety assessments will be made on several occasions throughout the whole study
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