Investigation on Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of NN9924 in Healthy Male Subjects

• Status: Completed
• Trial end date: 2011-07-01
• Target enrollment: 0
• Participant gender: Male

Summary

This trial is conducted in Europe. The aim of the trial is to investigate safety, tolerability, pharmacokinetics (the rate at which the body eliminates the trial drug) and pharmacodynamics (the effect of the investigated drug on the body) of NN9924 in healthy male subjects

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Novo Nordisk A/S

Criteria

Inclusion Criteria:

• Healthy male subjects, based on an assessment of medical history, physical examination and

• BMI between 21 and 30 kg/m2 (21 inclusive)

Exclusion Criteria:

• Male subjects who are sexually active and unwilling to use a highly effective method of contraception for both them and their nonpregnant partner

• Any clinically significant, abnormal disease history of the following systems:

cardio-pulmonary, gastrointestinal, hepatic, neurological, renal,genitourinary, endocrine or haematological

• The receipt of any investigational product within 90 days before screening, or is currently enrolled in any other clinical trial