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This is an open-label, single-dose, sequentially designed, single-period study to determine the effect of moderate renal impairment on the pharmacokinetics (PK) of CTP-543 and its major metabolites following administration of a single 12 mg oral dose of CTP-543.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| CTP-543 Treatment | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| CTP-543 | Drug | Single 12 mg oral dose administered on Day 1 |
|
| Measure | Description | Time Frame |
|---|---|---|
| Single dose PK exposure: Maximum observed concentration (Cmax) | Maximum concentration, obtained directly from the observed concentration versus time data. | 0 (pre-dose), 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 18, 24, 36, 48 hours post-dose |
| Single dose PK exposure: Area Under the Concentration-Time Curve from time zero to the time of the last observed/measured non-zero concentration (AUC0-t) | Area under the concentration-time curve from time zero (pre-dose) to time of last measurable concentration (calculated by linear-log trapezoidal summation) | 0 (pre-dose), 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 18, 24, 36, 48 hours post-dose |
| Single dose PK exposure: Area Under the Concentration-Time Curve from time 0 extrapolated to infinity (AUC0-inf) | Area under the concentration-time curve from time zero (pre-dose) extrapolated to infinity, calculated by linear-log trapezoidal summation and extrapolated to infinity by addition of the last quantifiable concentration divided by the elimination rate constant | 0 (pre-dose), 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 18, 24, 36, 48 hours post-dose |
| Measure | Description | Time Frame |
|---|---|---|
| Assessment of Safety and Tolerability following administration of CTP-543 | Number of adverse events, including abnormal clinical laboratory findings, abnormal physical examinations, abnormal ECGs and abnormal vital signs tabulated for each subject | Screening (within 21 days prior to Day 1) through follow-up (7 to 10 days after final drug) |
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Inclusion Criteria:
Additional Inclusion Criteria for Subjects with Renal Impairment:
Exclusion Criteria:
Additional Exclusion Criteria for Subjects with Renal Impairment:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Orlando Clinical Research Center | Orlando | Florida | 32809 | United States | ||
| Alliance for Multispecialty Research, LLC |
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| ID | Term |
|---|---|
| D051437 | Renal Insufficiency |
| ID | Term |
|---|---|
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
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| Knoxville |
| Tennessee |
| 37920 |
| United States |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |