Multicenter, randomized, controlled, open-label, Phase 3 study designed to demonstrate that neladalkib (NVL-655) is superior to alectinib in prolonging progression-free survival (PFS) in patients with treatment-naïve, Anaplastic Lymphoma Kinase (ALK) positive, advanced Non-Small Cell Lung Cancer (NSCLC).
Patients will be randomized in a 1:1 ratio (approximately 225 in each arm) to receive either neladalkib (NVL-655) or alectinib.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
450
Oral tablet of Neladalkib (NVL-655)
Oral capsule of alectinib
Progression-free survival (PFS) per blinded independent central review (BICR)
Time from randomization to BICR-assessed radiographic disease progression or death
Time frame: Up to 5 years after first patient dosed
Overall survival (OS)
Time from randomization to death
Time frame: Up to 5 years after first patient dosed
Progression-free survival (PFS) per investigator assessment
Time from randomization to investigator-assessed radiographic disease progression or death
Time frame: Up to 5 years after first patient dosed
Time to intracranial progression per BICR
Time from randomization to the first BICR-assessed occurrence of disease progression in the central nervous system (CNS)
Time frame: Up to 5 years after first patient dosed
Intracranial objective response rate (IC-ORR)
Proportion of patients with a confirmed intracranial response (intracranial complete response \[IC-CR\] or intracranial partial response \[IC-PR\]) among patients with measurable CNS disease at baseline
Time frame: Up to 5 years after first patient dosed
Intracranial duration of response (IC-DOR)
Time from first intracranial response (IC-CR or IC-PR) to radiographic intracranial disease progression or death
Time frame: Up to 5 years after first patient dosed
Objective response rate (ORR)
Proportion of patients with a complete response or partial response
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Palo Verde Hematology Oncology
Glendale, Arizona, United States
RECRUITINGUniversity of California, Irvine Health
Orange, California, United States
RECRUITINGRocky Mountain Cancer Centers
Denver, Colorado, United States
RECRUITINGSylvester Comprehensive Cancer Center Miami
Miami, Florida, United States
RECRUITINGAdventHealth Cancer Institute
Orlando, Florida, United States
RECRUITINGH Lee Moffitt Cancer Center and Research Institute
Tampa, Florida, United States
RECRUITINGWinship Cancer Institute of Emory University
Atlanta, Georgia, United States
RECRUITINGDana-Farber Cancer Institute
Boston, Massachusetts, United States
RECRUITINGBarbara Ann Karmanos Cancer Institute
Detroit, Michigan, United States
RECRUITINGWashington University Center for Advanced Medicine
St Louis, Missouri, United States
RECRUITING...and 102 more locations
Time frame: Up to 5 years after first patient dosed
Duration of response (DOR)
Time from first response (complete or partial) to radiographic disease progression or death
Time frame: Up to 5 years after first patient dosed
Intracranial progression per investigator assessment
Time to investigator-assessed intracranial progression
Time frame: Up to 5 years after first patient dosed
Treatment-emergent adverse events (TEAEs) and changes in clinically relevant laboratory parameters
Incidence and severity of TEAEs and changes in clinically relevant laboratory parameters
Time frame: Up to 5 years after first patient dosed
Patient-reported measures in health-related quality of life (QoL)
Changes in patient-reported outcomes (PROs) assessed by the European Organization for Research and Treatment of Cancer QoL core questionnaire - Cancer (EORTC QLQ-C30)
Time frame: Up to 5 years after first patient dosed
Patient-reported measures in lung cancer symptoms and side effects of treatment
Changes in PROs assessed by the European Organization for Research and Treatment of Cancer QoL - Lung Cancer module (EORTC QLQ-LC29)
Time frame: Up to 5 years after first patient dosed
Patient-reported measures in patient functioning
Changes in PROs assessed by the European Quality of Life (EuroQol) 5-dimension questionnaire (EQ-5D-5L)
Time frame: Up to 5 years after first patient dosed