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An External Control Arm Study in Non-Small Cell Lung Cancer

RecruitingObservational study

A Prospective Study to Generate Precision External Controls in Advanced or Metastatic Non Small Cell Lung Cancer Patients

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

1. \> 18 years of age at the time of informed consent
2. Pathologically confirmed locally advanced or metastatic NSCLC
3. ECOG Performance of less than or equal to 1 within 4 weeks prior to starting index therapy.
4. Life expectancy of more than 3 months
5. Able to understand and sign informed consent
6. Evidence of measurable disease (as assessed by the Investigator) on available imaging (e.g CT, MRI, PET)

\*see protocol for cohort specific inclusion criteria\*

Exclusion Criteria:

1. Actively on a clinical trial of an investigational agent
2. Currently receiving active systemic therapy for another malignancy
3. Eligible for treatment with curative intent

\*see protocol for cohort specific exclusion criteria\*

About the study

A study to create control arms using current and future information in patients with lung cancer.

Sponsor: N-Power Medicine · Participants: 650 · Started: Jan 7, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07174388

Locations in the U.S.

CaliforniaPacific Cancer Care, Monterey
DelawareBayhealth Medical Center, Kent Campus, Dover
Bayhealth Medical Center- Sussex Campus, Milford
IllinoisNorthwest Oncology and Hematology, Barrington
Northwest Oncology and Hematology, Elk Grove
Northwest Oncology and Hematology, Hoffman Estates
Northwest Oncology and Hematology, Rolling Meadows
New MexicoNew Mexico Oncology Hematology Consultants, Albuquerque
New YorkNew York Cancer and Blood Specialists, New York
PennsylvaniaMain Line Health, Wynnewood
TexasOncology Consultants, Houston

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.