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:

  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

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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Page 1 of 35 (137 locations)

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