Status:
RECRUITING
Neladalkib (NVL-655) for TKI-naive Patients With Advanced ALK-Positive NSCLC
Lead Sponsor:
Nuvalent Inc.
Conditions:
Non-small Cell Lung Cancer
Anaplastic Lymphoma Kinase-positive
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
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...
Detailed Description
Patients will be randomized in a 1:1 ratio (approximately 225 in each arm) to receive either neladalkib (NVL-655) or alectinib.
Eligibility Criteria
Inclusion Criteria:
- Histologically or cytologically confirmed locally advanced (not amenable for multimodality treatment) or metastatic Non-small Cell Lung Cancer (NSCLC)
- Documented Anaplastic Lymphoma Kinase (ALK) rearrangement via testing of tissue or blood
- No prior systemic anticancer treatment for NSCLC (adjuvant/neoadjuvant chemotherapy allowed if 12 months prior to randomization; prior ALK tyrosine kinase inhibitor [TKI] such as alectinib is not allowed in any setting)
- Measurable disease (1 or more target lesions per Response Evaluation Criteria in Solid Tumors [RECIST] 1.1)
- Pretreatment tumor tissue
Exclusion Criteria:
- Patient's cancer has a known oncogenic driver alteration other than ALK.
- Known allergy/hypersensitivity to excipients of neladalkib or alectinib.
- Ongoing or recent radiotherapy as per protocol-specified timeframes prior to randomization
- Major surgery within 4 weeks prior to randomization
- Uncontrolled clinically relevant infection requiring systemic therapy
- Known active tuberculosis, or active Hepatitis B or C
- QT corrected for heart rate by Fridericia's formula (QTcF) > 470 msec on repeated assessments
- Clinically significant cardiovascular disease
- Brain metastases associated with progressive neurological symptoms or requiring increasing doses of corticosteroids to control CNS disease
- Active malignancy requiring therapy within 2 years prior to randomization
Key Trial Info
Start Date :
July 17 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2029
Estimated Enrollment :
450 Patients enrolled
Trial Details
Trial ID
NCT06765109
Start Date
July 17 2025
End Date
December 1 2029
Last Update
March 24 2026
Active Locations (137)
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1
Palo Verde Hematology Oncology
Glendale, Arizona, United States, 85304
2
Hoag Hospital Newport Beach
Newport Beach, California, United States, 92663
3
University of California, Irvine Health
Orange, California, United States, 92868
4
Rocky Mountain Cancer Centers
Boulder, Colorado, United States, 80218