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NCT06568939 | RECRUITING | Non-Small Cell Lung Cancer

A Study to Assess Adverse Events and How Intravenously (IV) Infused Telisotuzumab Vedotin (ABBV-399) Moves Through the Body as a Monotherapy in Adult Participants With Previously Treated Non-Squamous Non-Small Cell Lung Cancer (NSCLC)
Sponsor:

AbbVie

Brief Summary:

Cancer is a condition where cells in a specific part of body grow and reproduce uncontrollably. Non-small cell lung cancer (NSCLC) is a solid tumor, a disease in which cancer cells form in the tissues of the lung. The purpose of this study is to assess how safe telisotuzumab vedotin is in adult participants with NSCLC. Change in disease activity and adverse events will be assessed. Telisotuzumab vedotin is an investigational drug being developed for the treatment of NSCLC. Participants will be randomly assigned a treatment of Teliso-V in 1 of 2 arms at an 1:1 ratio. Each group receives intravenous (IV) infusion of telisotuzumab vedotin. Approximately 100 adult participants with c-Met overexpressing NSCLC will be enrolled in the study at approximately 40 sites worldwide. Participants will receive IV telisotuzumab vedotin at 1 of 2 doses as part of a 3 year study duration. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.

Condition or disease

Non-Small Cell Lung Cancer

Intervention/treatment

Telisotuzumab Vedotin

Phase

PHASE2

Study Type : INTERVENTIONAL
Estimated Enrollment : 100 participants
Masking : NONE
Primary Purpose : TREATMENT
Official Title : A Phase 2, Open-Label, Randomized, Global Study of Two Telisotuzumab Vedotin Regimens in Subjects With Previously Treated c-Met Overexpressing, EGFR Wildtype, Locally Advanced/Metastatic Non-Squamous Non-Small Cell Lung Cancer
Actual Study Start Date : 2025-01-20
Estimated Primary Completion Date : 2028-02
Estimated Study Completion Date : 2028-02

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Projected life expectancy of at least 12 weeks.
  • * Must have c-Met overexpressing non-small cell lung cancer (NSCLC) as assessed by an AbbVie designated immunohistochemistry (IHC) laboratory
  • * Must have histologically or cytologically documented NSCLC that is locally advanced or metastatic.
  • * Must have a known epidermal growth factor receptor (EGFR) activating mutation status.
  • * Actionable alterations in genes other than EGFR are permitted.
  • * Must have measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
  • * Must have an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 1.
  • * Must have received no more than 1 line of prior systemic cytotoxic chemotherapy in the locally advanced or metastatic setting, as stated in the protocol.
  • * Must have progressed on at least 1 line of prior therapy for locally advanced/metastatic NSCLC, as stated in the protocol.
Exclusion Criteria
  • * Adenosquamous or neuroendocrine histology, or sarcomatoid features.
  • * Actionable EGFR activating mutations.
  • * Received prior c-Met-targeted antibodies, prior telisotuzumab vedotin, or prior antibody-drug conjugates either targeting c-Met or consisting of monomethylauristatin E.
  • * Received prior docetaxel therapy.
  • * Metastases to the central nervous system (CNS) are eligible only after adequate treatment (such as surgery or, radiotherapy, or drug therapy) is provided, as stated on the protocol.
  • * History of other malignancies except those stated in the protocol.
  • * History of idiopathic pulmonary fibrosis, organizing pneumonia (e.g., bronchiolitis obliterans), drug-induced pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis on screening chest computed tomography (CT) scan, as noted in the protocol.
  • * Unresolved clinically significant adverse event (AE) \>= Grade 2 from prior anticancer therapy, except for alopecia or anemia. Participants with hormone deficiencies caused by prior anticancer therapy who are asymptomatic and on a stable dose of replacement hormone are eligible for study.
  • * Major surgery within 21 days prior to randomization.
  • * Clinically significant condition(s) including but not limited to those listed in the protocol.
  • * Clinically significant liver disease, including hepatitis, current alcohol abuse, or cirrhosis.
  • * Grade \>= 2 edema or lymphedema.
  • * Grade \>= 2 ascites or pleural effusion.
  • * Grade \>= 2 neuropathy.
  • * Active uncontrolled bacterial or viral infection.
  • * Active corneal disorder.
A Study to Assess Adverse Events and How Intravenously (IV) Infused Telisotuzumab Vedotin (ABBV-399) Moves Through the Body as a Monotherapy in Adult Participants With Previously Treated Non-Squamous Non-Small Cell Lung Cancer (NSCLC)

Location Details

NCT06568939

Please Choose a site

How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations

RECRUITING

United States, Florida

Cancer Specialists of North Florida - Jacksonville - AC Skinner Parkway /ID# 270899

Jacksonville, Florida, United States, 32256

RECRUITING

United States, Florida

Comprehensive Hematology Oncology /ID# 270422

Saint Petersburg, Florida, United States, 33701-4732

RECRUITING

United States, Illinois

Springfield Clinic /ID# 272576

Springfield, Illinois, United States, 62702-3749

RECRUITING

United States, New Jersey

Asterra Cancer which /ID# 272359

East Brunswick, New Jersey, United States, 08816-4096

RECRUITING

United States, New York

Clinical Research Alliance - Westbury /ID# 270455

Westbury, New York, United States, 11590

RECRUITING

United States, North Carolina

FirstHealth of the Carolinas- Speciality Center /ID# 272924

Pinehurst, North Carolina, United States, 28374

RECRUITING

United States, Ohio

Genesis Healthcare System /ID# 273361

Zanesville, Ohio, United States, 43701

RECRUITING

United States, Pennsylvania

Guthrie Robert Packer Hospital /ID# 270316

Sayre, Pennsylvania, United States, 18840

RECRUITING

United States, Washington

Northwest Medical Specialties Tacoma /ID# 270534

Tacoma, Washington, United States, 98405

RECRUITING

Israel, H_EFA

Rambam Health Care Campus /ID# 270078

Haifa, H_efa, Israel, 3525408

RECRUITING

Israel, Hamerkaz

Meir Medical Center /ID# 270071

Beyon Kfar Saba, Hamerkaz, Israel, 4428164

RECRUITING

Israel,

Shaare Zedek Medical Center /ID#

Jerusalem, Israel, 9103102

RECRUITING

Israel,

Rabin Medical Center /ID# 270087

Heels of a tip, Israel, 4941492

RECRUITING

Singapore, Central Singapore

National Cancer Centre Singapore /ID# 271499

Singapore, Central Singapore, Singapore, 169611