NCT06745882
Prospective Trial Assessing Real World Outcomes Response to Pembro in Black Patients w/ NSCLC
Recruiting
PHASE2Ages 18+InterventionalTreatmentH. Lee Moffitt Cancer Center and Research InstituteInvestigator-initiated
~318 participants
Updated 2026-08-26 on ClinicalTrials.gov
What's tested:CisplatinCarboplatinPemetrexedPembrolizumabAbraxanePaclitaxel
At a glance
Recruiting sites
8 of 8 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Cohort 1: Real World Overall Survival (rwOS)
Measured over Up to 36 Months
+2 more outcomes measured
Conditions
Where it's being run
8 sites across 6 statesMaryland2
Tennessee2
Florida1
Louisiana1
New York1
North Carolina1
Study leadership
- Jhanelle Gray, MD · PRINCIPAL_INVESTIGATOR · Moffitt Cancer Center
Who to contact
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Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Eligibility criteria
Inclusion
Be willing and able to provide written informed consent/assent.
Must be ≥ 18 years of age on day of signing informed consent.
Be Black / African American per self-report.
Have an ECOG performance status of 0- 2.
Have histologically or cytologically confirmed, advanced/metastatic NSCLC.
Be treatment naïve in the advanced/metastatic/recurrent disease setting.
No known EGFR/ALK/ROS1 tumor mutations. Liquid biopsies are acceptable.
Patients who received platinum-containing adjuvant chemotherapy, neoadjuvant chemotherapy or definitive chemoradiation and/or neoadjuvant and/or adjuvant immunotherapy and/or consolidation immunotherapy therapy given for locally advanced disease and developed recurrent (local or metastatic) disease ≥ 6 months of completing therapy are eligible.
Be planned/eligible to receive first-line therapy in the advanced/metastatic setting.
Have testing status for PDL1 tissue status.
Participants who have AEs due to previous anticancer therapies must have recovered to ≤Grade 1 or baseline. Participants with any grade endocrine-related AEs who are adequately treated with hormone replacement or participants who have ≤Grade 2 neuropathy are eligible.
Adequate organ function.
Female subjects of childbearing potential should have a negative urine or serum pregnancy within 72 hours prior to receiving the first dose of study medication. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
Female subjects of childbearing potential should be willing to use 2 methods of birth control or be surgically sterile or abstain from heterosexual activity for the course of the study through 180 days after the last dose if treated with pembrolizumab plus chemotherapy, or 120 days after the last dose if treated with pembrolizumab monotherapy. Subjects of childbearing potential are those who have not been surgically sterilized or have not been free from menses for \> 1 year.
Male subjects should agree to use an adequate method of barrier contraception starting with the first dose of study therapy through 180 days after the last dose if treated with pembrolizumab plus chemotherapy.
Exclusion
Does not plan or is ineligible to receive pembrolizumab with or without chemotherapy per institutional standard/treating provider.
History of allogenic tissue/solid organ transplant.
Received prior treatment chemotherapy and/or immune checkpoint inhibitor therapy in the advanced/metastatic setting for lung cancer.
Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy at doses
Has active autoimmune disease that has required active systemic treatment in the past 2 years \[i.e., with use of disease modifying agents, corticosteroids in doses greater than 10 mg of prednisone daily (or equivalent) or immunosuppressive drugs\]. Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment.
Subjects are permitted to enroll if they have vitiligo, type I diabetes mellitus, residual hypothyroidism due to autoimmune condition only requiring hormone replacement, psoriasis not requiring systemic treatment, or conditions not expected to recur in the absence of an external trigger.
Has an active infection requiring systemic therapy.
Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, that would substantially increase the risk of incurring adverse events (AEs) from the study medications, that would interfere with the subject's participation for the full duration of the study or is not in the best interest of the subject to participate, in the opinion of the treating investigator.
Has received a live vaccine within 30 days of planned start of study therapy.
Has received an investigational agent or has used an investigational device within 3 weeks prior to study intervention administration.
History of (noninfectious) pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease.
Has known untreated central nervous system (CNS) metastases and/or carcinomatous meningitis. Participants with previously treated brain metastases may participate provided they have completed radiation therapy (where applicable), are clinically stable and have not required steroid treatment at ≥ 10 mg of prednisone for at least 3 days prior to the first dose of study intervention.
Severe hypersensitivity (≥ Grade 3) to pembrolizumab and/or any of its excipients or has a known sensitivity as applicable to carboplatin, cisplatin, taxane or pemetrexed.
What this trial measures
- Cohort 1: Real World Overall Survival (rwOS)Up to 36 Months
Real-world overall survival (rwOS) is defined as the length of time from the date the patient initiates treatment to the date of death or end of follow up, whichever occurred earliest.
- Cohort 2 Arm A: Progression Free Survival (PFS)Up to 36 Months
Progression free survival is defined as the length of time from date of patient starts treatment to date of progression event or death.
- Cohort 2 Arm B: Progression Free Survival (PFS)Up to 36 Months
Progression free survival is defined as the length of time from date of patient starts treatment to date of progression event or death.