Renal Impairment
Conditions
Keywords
CTP-543
Brief summary
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.
Interventions
DRUGCTP-543
Single 12 mg oral dose administered on Day 1
Sponsors
Concert Pharmaceuticals
Study design
Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes
Inclusion criteria
* Adult males or females aged 18-75 * Body mass index (BMI) ≥ 18.0 and ≤ 42.0 kg/m2 at the time of screening * If of reproductive age, willing and able to use a medically highly effective form of birth control 30 days prior to first dose, during the study and for 30 days following last dose of study medication * Capable of giving informed consent and complying with study procedures Additional Inclusion Criteria for Subjects with Renal Impairment: * eGFR of 30-59 mL/minute/1.73 m2 as calculated by the MDRD equation * No clinically significant change in disease status within the last 30 days before screening * The subject must have a condition consistent with renal impairment and associated symptoms, but otherwise be determined to be in good health in the opinion of the Investigator * Concomitant medications to treat underlying disease states or medical conditions related to renal impairment are allowed with the exception of strong CYP3A4 inhibitors and inducers
Exclusion criteria
* History of any clinically significant medical condition, psychiatric disease, social condition, or illness that might confound the results of the study or poses an additional risk to the subject by their participation in the study * Known history of any gastrointestinal surgery or any condition possibly affecting drug absorption * History of prolonged QT syndrome or a QTc interval with Fridericia's correction (QTcF) \> 470 msec for males or QTcF \> 480 msec for females at Screening visit * Positive for human immunodeficiency virus, Hepatitis B virus, or Hepatitis C virus * Females who are nursing or pregnant prior to drug administration * Positive results for coronavirus infection (COVID-19) at screening or check-in * Positive drugs of abuse or alcohol results at screening or check in (Day -1) Additional
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Single dose PK exposure: Maximum observed concentration (Cmax) | 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 | Maximum concentration, obtained directly from the observed concentration versus time data. |
| 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) | 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 | Area under the concentration-time curve from time zero (pre-dose) to time of last measurable concentration (calculated by linear-log trapezoidal summation) |
| Single dose PK exposure: Area Under the Concentration-Time Curve from time 0 extrapolated to infinity (AUC0-inf) | 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 | 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 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Assessment of Safety and Tolerability following administration of CTP-543 | Screening (within 21 days prior to Day 1) through follow-up (7 to 10 days after final drug) | Number of adverse events, including abnormal clinical laboratory findings, abnormal physical examinations, abnormal ECGs and abnormal vital signs tabulated for each subject |
Countries
United States
Outcome results
None listed