This trial is conducted in Asia. The aim of this clinical trial is to investigate the pharmacokinetic properties (the rate at which the trial drug is eliminated from the body) after a single subcutaneous (under the skin) injection of biphasic insulin aspart 50 (BIAsp 50). In addition, the safety and tolerability of BIAsp 50 will be observed
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
24
A single dose of 0.3 U/kg BIAsp 50 for subcutaneous (under the skin) injection
Unnamed facility
Beijing, Beijing Municipality, China
Area under the serum insulin aspart concentration-time curve from 0 to 24hours
Time frame: 24 hours profile after single dose of trial drug
Area under the serum insulin aspart concentration-time curve between different time intervals
Time frame: 24 hours profile after single dose of trial drug
Maximum observed serum insulin aspart concentration
Time frame: 24 hours profile after single dose of trial drug
Number of adverse events.
Time frame: After 3-10 days of treatment
Number of hypoglycaemic events
Time frame: After 3-10 days of treatment
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