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Neladalkib (NVL-655) for TKI-naive Patients With Advanced ALK-Positive NSCLC

RecruitingPhase 3

A Phase 3 Study of the Selective Anaplastic Lymphoma Kinase (ALK) Inhibitor NVL-655 Compared to Alectinib in First-Line Treatment of Patients With ALK-Positive Advanced Non-Small Cell Lung Cancer (ALKAZAR)

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

1. Histologically or cytologically confirmed locally advanced (not amenable for multimodality treatment) or metastatic Non-small Cell Lung Cancer (NSCLC)
2. Documented Anaplastic Lymphoma Kinase (ALK) rearrangement via testing of tissue or blood
3. 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)
4. Measurable disease (1 or more target lesions per Response Evaluation Criteria in Solid Tumors \[RECIST\] 1.1)
5. Pretreatment tumor tissue

Exclusion Criteria:

1. Patient's cancer has a known oncogenic driver alteration other than ALK.
2. Known allergy/hypersensitivity to excipients of neladalkib or alectinib.
3. Ongoing or recent radiotherapy as per protocol-specified timeframes prior to randomization
4. Major surgery within 4 weeks prior to randomization
5. Uncontrolled clinically relevant infection requiring systemic therapy
6. Known active tuberculosis, or active Hepatitis B or C
7. QT corrected for heart rate by Fridericia's formula (QTcF) \> 470 msec on repeated assessments
8. Clinically significant cardiovascular disease
9. Brain metastases associated with progressive neurological symptoms or requiring increasing doses of corticosteroids to control CNS disease
10. Active malignancy requiring therapy within 2 years prior to randomization

About the study

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).

What is being tested

Sponsor: Nuvalent Inc. · Participants: 450 · Started: Jul 17, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT06765109

Locations in the U.S.

ArizonaPalo Verde Hematology Oncology, Glendale
CaliforniaHoag Hospital Newport Beach, Newport Beach
University of California, Irvine Health, Orange
ColoradoRocky Mountain Cancer Centers, Boulder
FloridaSylvester Comprehensive Cancer Center Miami, Miami
AdventHealth Cancer Institute, Orlando
H Lee Moffitt Cancer Center and Research Institute, Tampa
GeorgiaWinship Cancer Institute of Emory University, Atlanta
MassachusettsDana-Farber Cancer Institute, Boston
MissouriWashington University Center for Advanced Medicine, St Louis
New YorkMemorial Sloan Kettering Cancer Center, New York
NYU Langone's Perlmutter Cancer Center, New York
Optum Medical Care, PC, Westbury
North CarolinaCarolinas Medical Center, Charlotte
Duke Cancer Center, Durham
OhioUniversity of Cincinnati Cancer Center, Cincinnati
The Ohio State University, Columbus
PennsylvaniaAlliance Cancer Specialists, Sellersville
TennesseeSCRI Oncology Partners, Nashville
VirginiaVirginia Cancer Specialists, Fairfax
WashingtonUniversity of Washington - Fred Hutchinson Cancer Center, Seattle
Compass Oncology, Vancouver

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.