Study S001326
A Randomised, Double-blind, Placebo-controlled, Dose Escalation Trial of Single Subcutaneous Doses of NNC 0113-0217 to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics in Healthy Male Subjects
Registration
Registered primary outcomes
- Number of Adverse Events [After 24-33 days]
Linked records (0)
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