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| ID | Type | Description | Link |
|---|---|---|---|
| U1111-1173-7678 | Other Identifier | WHO |
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This trial is conducted in Asia. The aim of this trial is to investigate the pharmacokinetic (the exposure of the trial drug in the body) properties of insulin degludec/insulin aspart in healthy Chinese subjects.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| IDegAsp | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| insulin degludec/insulin aspart | Drug | A single dose of IDegAsp will be administered subcutaneously (s.c., under the skin). |
|
| Measure | Description | Time Frame |
|---|---|---|
| Area under the serum insulin degludec concentration-time curve | From 0 to 120 hours after single dose | |
| Area under the serum insulin aspart concentration-time curve | From 0 to 12 hours after single dose |
| Measure | Description | Time Frame |
|---|---|---|
| Maximum observed serum insulin degludec concentration | After single dose (within 0 to 120 hours after dosing) | |
| Maximum observed serum insulin aspart concentration | After single dose (within 0 to 12 hours after dosing) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Global Clinical Registry (GCR, 1452) | Novo Nordisk A/S | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Novo Nordisk Investigational Site | Beijing | 100730 | China |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| Background | Aixin S, Yang L, Panpan X, Qi W , Lei Y, Hongfei X, Ran LZ, Haahr H. A study investigating the pharmacokinetic properties of insulin degludec/insulin aspart in healthy Chinese subjects. Diabetes Manag. 2019; 9 (2): 48-56. |
| Label | URL |
|---|---|
| Clinical Trials at Novo Nordisk | View source |
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| ID | Term |
|---|---|
| C578220 | insulin degludec, insulin aspart drug combination |
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| Time to maximum observed serum insulin degludec concentration | After single dose (within 0 to 120 hours after dosing) |
| Time to maximum observed serum insulin aspart concentration | After single dose (within 0 to 12 hours after dosing) |