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| Name | Class |
|---|---|
| Pfizer | INDUSTRY |
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The purpose of this study is to assess the effect of Atenolol 100 mg on the Pharmacokinetics (PK) of Apixaban and the effect of Apixaban 10 mg on the PK of Atenolol in Healthy subjects.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Treatment A: Apixaban | Experimental | Apixaban tablet by mouth on specified day |
|
| Treatment B: Atenolol | Experimental | Atenolol tablet by mouth on specified day |
|
| Treatment C: Apixaban and Atenolol | Experimental | Apixaban and Atenolol tablets by mouth on specified day |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Apixaban | Drug |
| ||
| Atenolol |
| Measure | Description | Time Frame |
|---|---|---|
| Apixaban and Atenolol plasma concentration | Blood samples for Atenolol PK were collected on days 1-3 of each period (Treatment B and C). Blood samples for Apixaban PK were collected on days 1-4 of each period (Treatment A and C) | Days 1-13 |
| Measure | Description | Time Frame |
|---|---|---|
| Safety and Tolerability based on adverse events (AE) reports and the results of vital sign measurements, electrocardiogram (ECGs), physical examinations, and clinical laboratory tests | Days 1-13 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Bristol-Myers Squibb | Bristol-Myers Squibb | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Bms Clinical Research Center | Hamilton | New Jersey | 08690 | United States |
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| ID | Term |
|---|---|
| C522181 | apixaban |
| D001262 | Atenolol |
| ID | Term |
|---|---|
| D050198 | Phenoxypropanolamines |
| D011412 | Propanolamines |
| D000605 | Amino Alcohols |
| D000438 | Alcohols |
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| Drug |
|
| D009930 |
| Organic Chemicals |
| D020005 | Propanols |
| D000588 | Amines |