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The purpose of this study is to study the relative bioavailability of AZD1981 when using a new tablet compared to the current tablet.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Treatment A | Experimental |
| |
| Treatment B | Experimental |
| |
| Treatment C | Experimental |
| |
| Treatment D | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| AZD1981, current small-particle tablet | Drug | 3x100 mg per oral, single dose in fasted state |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Assessment of the area under the plasma concentration time-curve from zero to infinity /AUC) and the maximum plasma concentration (Cmax) of AZD1981 | Pharmacokinetic (PK) sampling continuously for 60 h after each single dose, ie day 1-3 for each period. |
| Measure | Description | Time Frame |
|---|---|---|
| To evaluate basic systemic PK parameters as follows: |
| PK sampling continuously for 60 h after each single dose, ie day 1-3 for each period |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Wolfgang Kühn, MD | Quintiles AB, Phase 1 Services | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Research Site | Uppsala | Sweden |
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| ID | Term |
|---|---|
| C569518 | AZD1981 |
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| AZD1981, new small-particle tablet |
| Drug |
3x100 mg per oral, single dose |
|
| AZD1981, new large-particle table | Drug | 3x100 mg per oral, single dose in fasted state |
|
| To evaluate the safety and tolerability of AZD1981 by assessment of adverse events, laboratory safety parameters, vital signs, ECG, physical examination and weight | Safety will be monitored continuously and safety assessments will be made on several occasions throughout the whole study |