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NCT07795411Recruiting

Prospective Multiomic Analysis in Small-Cell Lung Cancer

Prospective Multiomic Analysis in Small-Cell Lung Cancer to Inform Therapeutic Vulnerabilities and Predict Clinical Outcomes: Deep Phenotyping of Relapsed SCLC Cohort

Source: ClinicalTrials.gov · Last updated 2 Oct 2026

Brief summary (registry, in English)

This is an observational study to collects blood samples and tumor tissue from adults with relapsed small-cell lung cancer (SCLC) receiving standard of care commercial DLL3 T cell engager. The goal of the study is to understand the changes in tumor markers over time and examine whether these changes are associated with clinical outcomes. Participants will provide blood samples and, when clinically feasible, tumor tissue during routine care visits, treatment, and imaging assessments. The study does not assign cancer treatment.

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
26 Aug 2026
Start date
25 Nov 2026
Primary completion date
31 Dec 2028
Lead sponsor
Ohio State University Comprehensive Cancer Center
Diseases
Lung cancer
NCT number
NCT07795411

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 25 Nov 2026 to the primary completion date, 31 Dec 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • There will be no specific restrictions with respect to performance status, organ function, or prior/concurrent modes of therapy other than that the patient must be able to tolerate venipuncture and any planned interventional radiology or surgical procedures deemed necessary by their treating physicians.

Other

  • Prisoners or incarcerated patients
  • Those with cognitive impairments lacking decision-making capacity are excluded.

Who the study is looking for

  • 18 years of age or older
  • Confirmed pathologic diagnosis of active SCLC or neuroendocrine cancer.
  • Relapsed small cell lung cancer (SCLC) planning to receive commercial DLL3 bispecific T cell engager.
  • Willing to provide informed consent.
  • Willing to provide blood samples and undergo tissue biopsy at various time points throughout the study, collected in concurrence with treatment cycles and/or imaging visits
  • Patients with multiple primary malignancies, recurrent lung cancer, or mixed histology are not excluded.
  • Patients who have contraindications or are unable to receive immunotherapy will be eligible for the study, and their samples will be used for comparison and control.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Ohio State University Comprehensive Cancer Center
Coordinator of this site? Confirm its status
ColumbusUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.