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Recruiting Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT07288177

Public ClinicalTrials.gov record NCT07288177. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 12:13 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Open-label, Multicohort Study of Rinatabart Sesutecan (Rina-S) in Participants With Non-Small Cell Lung Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT07288177
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Genmab
Industry
Enrollment
240 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 29, 2026
Primary completion
Nov 21, 2027
Completion
Nov 21, 2028
Last update posted
Aug 25, 2026

2026 – 2028

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Compassionate Cancer Care Center Fountain Valley California 92708 Recruiting
Kaiser Permanente San Diego Mission Road San Diego California 92108 Recruiting
Providence Medical Foundation (St. Joseph Heritage Healthcare) Santa Rosa California 95403 Recruiting
MedStar Georgetown University Hospital Washington D.C. District of Columbia 20007 Recruiting
Moffitt Cancer Center and Research Institute Tampa Florida 33612 Recruiting
Emory Winship Cancer Institute Atlanta Georgia 30322 Recruiting
St. Vincent Frontier Cancer Center Billings Montana 59102 Recruiting
Nebraska Hematology-Oncology Lincoln Nebraska 68506 Recruiting
Astera Cancer Care East Brunswick New Jersey 08816 Recruiting
ONE Onc: New York Oncology Hematology Albany New York 12206 Recruiting
Montefiore Medical Park The Bronx New York 10461 Recruiting
UNC Health - University of North Carolina Chapel Hill North Carolina 27514 Recruiting
Williamette Valley Cancer Institute and Research Center Eugene Oregon 97401 Recruiting
Providence Portland Medical Center Portland Oregon 97213 Recruiting
Providence Oncology & Hematology Care Clinic - Westside West Haven-Sylvan Oregon 97225 Recruiting
Tennessee Oncology - Nashville St. Thomas Midtown Clinic Nashville Tennessee 37203 Recruiting
Tennessee Oncology Nashville - SCRI Oncology Partners Nashville Tennessee 37203 Recruiting
Baylor Charles A. Sammons Cancer Center Dallas Texas 75246 Recruiting
Virginia Cancer Specialists Fairfax Virginia 22031 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 55 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07288177, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 25, 2026 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07288177 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →