This is a 3-cohort, multicenter, Phase 1 study of the effect of tesetaxel, an investigational, orally administered taxane, on the corrected QT (QTc) interval and the potential effect of food, a cytochrome P450 (CYP) 3A inhibitor (itraconazole), and a CYP3A inducer (rifampin) on tesetaxel pharmacokinetics (PK) in adult patients with advanced solid tumors.
Cohort 1: Cohort 1 is a 2-period, 2-sequence, crossover study designed to assess the effect of food on the PK of tesetaxel and tesetaxel metabolites. Patients were randomized in a 1:2 ratio to receive tesetaxel on Day 1 of two 21-day cycles under fed and fasting conditions in one of two opposing sequences (Sequence 1A and Sequence 1B). Cohort 2: Cohort 2 is a 2-period, single-sequence, crossover study designed to assess the potential PK drug-drug interaction (DDI) of a strong CYP3A inhibitor (itraconazole) on tesetaxel and tesetaxel metabolites. Patients receive tesetaxel during Cycle 1 followed by a reduced dose of tesetaxel plus itraconazole during Cycle 2. Cohort 3: Cohort 3 is a 2-period, single-sequence, crossover study designed to assess the potential PK DDI of a strong CYP3A inducer (rifampin) on tesetaxel and tesetaxel metabolites. Patients receive tesetaxel during Cycle 1 followed by tesetaxel plus rifampin during Cycle 2. Patients in all cohorts also participate in a study designed to assess the effect of tesetaxel and tesetaxel metabolites on cardiac repolarization as measured by the change from baseline in the QTc interval over the first cycle of treatment. Patients who are tolerating and benefitting from treatment with tesetaxel have the opportunity to continue onto an optional treatment extension.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
93
Tesetaxel orally on Day 1 of a 21-day cycle
Tesetaxel orally on Day 1 of a 21-day cycle
Itraconazole orally once daily from Day -3 to Day 14 of a 21-day cycle
START Midwest
Grand Rapids, Michigan, United States
Mary Crowley Cancer Research
Dallas, Texas, United States
NEXT Oncology
San Antonio, Texas, United States
All Cohorts: The change from baseline in Fridericia's corrected QT (ΔQTcF) interval
Time frame: Approximately 3 weeks
Cohort 1, Sequences 1A and 1B: Maximum observed plasma concentration (Cmax) for tesetaxel under fed and fasted conditions
Time frame: Approximately 6 weeks
Cohort 1, Sequences 1A and 1B: Area under the plasma concentration-time curve from 0 to the last measurable plasma concentration (AUC0-t) for tesetaxel under fed and fasted conditions
Time frame: Approximately 6 weeks
Cohort 2: Cmax for tesetaxel in the presence and absence of itraconazole
Time frame: Approximately 6 weeks
Cohort 2: AUC from 0 to 336 hours (AUC0-336h) for tesetaxel in the presence and absence of itraconazole
Time frame: Approximately 6 weeks
Cohort 3: Cmax for tesetaxel in the presence and absence of rifampin
Time frame: Approximately 6 weeks
Cohort 3: AUC0-336h for tesetaxel in the presence and absence of rifampin
Time frame: Approximately 6 weeks
All Cohorts: Cmax for tesetaxel metabolites
Time frame: Approximately 6 weeks
All Cohorts: AUC for tesetaxel metabolites
Time frame: Approximately 6 weeks
All Cohorts: Treatment-emergent adverse events (TEAEs), including serious adverse events (SAEs)
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Rifampin orally once daily from Day -6 to Day 14 of a 21-day cycle
Time frame: Baseline through 30 days after last administration of Study treatment