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RecruitingNon-small Cell Lung Cancer (NSCLC)

Study to Assess the Efficacy and Safety of Rina-S in Participants With Non-small Cell Lung Cancer

Eligible age

18+ yrs

Accepts

All genders

Locations

12 states

Healthy volunteers

No

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About this study

This Phase 2 study will be conducted in different countries around the world with up to about 240 participants. The purpose of this study is to evaluate how well Rina-S works against lung cancer. The treatment in this study is Rina-S monotherapy (by itself). All participants will receive active drug; no one will be given placebo. The treatment duration will be different for every participant, but an average of 12 months is expected. Participants will be asked to attend 1 to 5 visits at the study clinic for each cycle (duration of cycle is 3 weeks). If a participant's cancer stays the same or gets better, and there are not any serious problems, participants can keep getting study treatment for as long as the study is open. Participation in the study will require visits to the study site(s). During site visits, there will be various tests (such as blood draws) and procedures (such as recording of heart activity, imaging/X-rays) to monitor whether the study treatment is safe and effective.

Sponsor: Genmab

Where it's recruiting

California

Fountain Valley · Santa Rosa

District of Columbia

Washington D.C.

Florida

Tampa

Georgia

Atlanta

Montana

Billings

Nebraska

Lincoln

New Jersey

East Brunswick

New York

Albany · The Bronx

North Carolina

Chapel Hill

Oregon

Portland · West Haven-Sylvan

Tennessee

Nashville

Virginia

Fairfax

Source: ClinicalTrials.gov · NCT07288177 · last updated 2026-08-04

Study to Assess the Efficacy and Safety of Rina-S in Participants With · TrialPath