Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

ACTIVE NOT RECRUITING Phase 3

Zimberelimab and Domvanalimab in Combination With Chemotherapy Versus Pembrolizumab With Chemotherapy in Patients With Untreated Metastatic Non-Small Cell Lung Cancer

NCT05502237 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to compare the effect of zimberelimab (ZIM) and domvanalimab (DOM) in combination with chemotherapy relative to pembrolizumab (PEMBRO) in combination with chemotherapy on overall survival (OS) in patients with untreated metastatic non-small cell lung cancer with no actionable genomic alteration.

Conditions Studied

Interventions

  • DRUG Pembrolizumab
  • DRUG Carboplatin
  • DRUG Cisplatin
  • DRUG Zimberelimab
  • DRUG Domvanalimab

Study Locations (20)

Other

  • Investigaciones CORI S.R.L. — Capital
  • Centro Médico Privado Centro de Especialidades Médicas Ambulatorias e Investigación Clínica — Cardoba
  • Sanatorio Allende — Córdoba
  • Sanatorio Britanico de Rosario — Rosario
  • Sanatorio Parque de Rosario — Rosario
  • Hospital Provincial del Centenario — Rosario
  • Instituto Medico de la Fundacion Estudios Clinicos — Rosario
  • Clínica Viedma — Viedma
  • Ordensklinikum Linz GmbH, Elisabethinen — Linz

California

  • Innovative Clinical Research Institute — Whittier

District of Columbia

  • George Washington Medical Faculty Associates — Washington D.C.

Florida

  • Moffitt Cancer Center — Tampa

Illinois

  • Illinois Cancer Care — Peoria

North Carolina

  • Messino Cancer Centers — Asheville

Ohio

  • Oncology Hematology Care, Inc. — Cincinnati

Oregon

  • Hematology & Oncology Associates — Eugene

Trial Details

FieldValue
Enrollment Target 1,021 participants
Start Date 2022-10-12
Est. Completion 2029-01
Phase Phase 3

Sponsor

Gilead Sciences

190 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05502237

The ClinicalTrials.gov registry entry for NCT05502237 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,021 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Gilead Sciences, which has 190 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Non-small Cell Lung Cancer appearing as the primary indexed condition, and to 5 interventions — of which Pembrolizumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05502237 reports 20 study locations spanning 12 distinct geographic areas — top geographies include Other, California, District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05502237 about?

NCT05502237 is a clinical study titled "Zimberelimab and Domvanalimab in Combination With Chemotherapy Versus Pembrolizumab With Chemotherapy in Patients With Untreated Metastatic Non-Small Cell Lung Cancer". The primary objective of this study is to compare the effect of zimberelimab (ZIM) and domvanalimab (DOM) in combination with chemotherapy relative to pembrolizumab (PEMBRO) in combination with chemotherapy on overall survival (OS) in patients with untreated metastatic non-small cell lung cancer wit...

What is the current status of trial NCT05502237?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 1,021 participants. The study started on 2022-10-12. Estimated completion is 2029-01.

What conditions does trial NCT05502237 study?

This clinical trial studies the following conditions: Non-small Cell Lung Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05502237?

The interventions under investigation include: Pembrolizumab (DRUG), Carboplatin (DRUG), Cisplatin (DRUG), Zimberelimab (DRUG), Domvanalimab (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05502237?

This trial is sponsored by Gilead Sciences, which has 190 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05502237 being conducted?

This trial has 20 study locations across California, District of Columbia, Florida, Illinois, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial