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Study to evaluate the effect of lapatinib, a breast cancer resistance protein (BCRP) inhibitor, on the pharmacokinetics (PK) of JTZ-951 and to evaluate the safety and tolerability of JTZ-951 when administered alone and one hour after the administration of lapatinib.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Experimental: JTZ-951 and Lapatinib | Experimental | Tablets; JTZ-951, single dose on non-dialysis Days 1 and 5; Lapatinib, single dose on non-dialysis Day 5 |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| JTZ-951 | Drug |
| ||
| Lapatinib |
| Measure | Description | Time Frame |
|---|---|---|
| Cmax (maximum concentration) | 10 days | |
| tmax (time to reach maximum concentration) | 10 days | |
| AUC (area under the concentration-time curve) | 10 days | |
| t1/2 (elimination half-life) | 10 days | |
| Number of adverse events | 10 days |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Minneapolis | Minnesota | United States |
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| ID | Term |
|---|---|
| C000656654 | enarodustat |
| D000077341 | Lapatinib |
| ID | Term |
|---|---|
| D011799 | Quinazolines |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
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