The purpose of this phase 3 multicenter double-blind randomized study is to assess the use of taletrectinib in the early-stage non-small cell lung cancer (NSCLC). The study compares taletrectinib (study drug) versus placebo (sugar pill) in patients with ROS1-fusion positive stage IB, II, IIIA NSCLC. The study will evaluate if taletrectinib is better than placebo at preventing the participant's disease from coming back after the participant's lung tumor was removed.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
180
Intervention Label: Taletrectinib Intervention Name: Taletrectinib Dosage Formulation: Capsule Unit Dose Strength(s): 200 mg Dosage Level (s): 400 mg QD Route of Administration: Oral Use: Experimental IMP and NIMP/AxMP : IMP Former Name(s) or Alias(es): AB-106.
Intervention Label: Placebo Intervention Name: Placebo Type: Drug Dosage Formulation: Capsule Unit Dose Strength(s): 200 mg Dosage Level(s): 400 mg QD Route of Administration: Oral Use: Placebo Comparator IMP and NIMP/AxMP: IMP Former Name(s) or Alias(es): Placebo
UCLA
Los Angeles, California, United States
RECRUITINGGeorgetown University Medical Cener (GUMC)
Washington D.C., District of Columbia, United States
RECRUITINGPrimary Outcome Measure: To compare the efficacy of taletrectinib with that of placebo, as measured by disease-free survival (DFS) by investigator assessment.
Measure Description: Defined as the time from the date of randomization until the date of disease recurrence or death (by any cause in the absence of recurrence) by investigator's assessment.
Time frame: Time Frame: Up to approximately 5 years after the first patient is randomized (maximum follow-up of 70 months).
Secondary Outcome Measure: DFS rates by investigator assessment at 2, 3, 4, and 5 years.
Measure Description: The percentage of participants disease free and alive as determined by investigator assessment at 2, 3, 4, and 5 years after date of randomization.
Time frame: Time Frame: Up to approximately 5 years after the first patient is randomized (maximum follow-up of 70 months). DFS rate 2 years (%), 3 years (%), 4 years (%), and 5 years (%) are presented.
Secondary Outcome Measure: Overall Survival (OS).
Measure Description: Defined as the time from the date of randomization until date of death due to any cause.
Time frame: Time Frame: Up to approximately 7 years after the first patient is randomized (maximum follow-up of 86 months).
Secondary Outcome Measure: DFS by blinded independent central review (BICR).
Measure Description: Defined as the time from the date of randomization until the date of disease recurrence of death (by any cause in the absence of recurrence) by blinded independent central review.
Time frame: Time Frame: Up to approximately 5 years after the first patient is randomized (maximum follow-up of 70 months).
Secondary Outcome Measure: OS rates at 2, 3, 4, and 5 years.
Measure Description: The percent of participants that are alive at 2, 3, 4, and 5 years after date of randomization.
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Saint Alphonsus Health System
Boise, Idaho, United States
RECRUITINGDana Farber Cancer Institute
Boston, Massachusetts, United States
RECRUITINGMayo Clinic
Rochester, Minnesota, United States
RECRUITINGMemorial Sloan Kettering Cancer Center
New York, New York, United States
RECRUITINGSarah Cannon Research Institute (SCRI) - Texas Oncology-Central South
Austin, Texas, United States
RECRUITINGMD Anderson
Houston, Texas, United States
RECRUITINGVirginia Cancer Specialists
Fairfax, Virginia, United States
RECRUITINGPrincess Margaret Cancer Centre-University Health Network
Toronto, Ontario, Canada
RECRUITINGTime frame: Time Frame: Up to approximately 7 years after the first patient is randomized (maximum follow-up of 86 months). DFS rate 2 years (%), 3 years (%), 4 years (%), and 5 years (%) are presented.
Secondary Outcome Measure: Central nervous system (CNS) DFS by Investigator assessment and by BICR.
Measure Description: Defined as the time from the date of randomization until the date of disease recurrence within the CNS or death (by any cause in the absence of recurrence) by investigator's assessment and blinded independent central review.
Time frame: Time Frame: Up to approximately 5 years after the first patient is randomized (maximum follow-up of 70 months).
Secondary Outcome Measure: Plasma concentrations of taletrectinib.
Measure Description: The pharmacokinetics exposure parameters derived from plasma concentrations of taletrectinib.
Time frame: Time Frame: Collected between 1-3 hours post-dose on Cycle1 Day 1, and pre-dose and 1-3 hours post-dose at Cycle 2 Day 1, and pre-dose at Cycle 4 Day 1, and Cycle 7 Day 1. The length of each cycle is 28 days.
Secondary Outcome Measure: Incidence of adverse events (AEs).
Measure Description: Defined as the number of patients reporting adverse events within one study arm compared to the overall number of patients within the same study arm.
Time frame: Time Frame: Up to approximately 5 years after the first patient is randomized (maximum follow-up of 70 months).