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RECRUITING Phase 2

KEYMAKER-U01 Substudy 01J: A Study of Pembrolizumab Plus MK-1084 in Participants With Non-Small Cell Lung Cancer (NSCLC) With Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS) G12C Mutations (MK-3475-01J/KEYMAKER-U01J)

NCT07252739 · View on ClinicalTrials.gov ↗

Study Summary

Researchers want to learn if using a study medicine called MK-1084 can help treat NSCLC. MK-1084 is a type of treatment called targeted therapy for the Kirsten rat sarcoma viral oncogene homolog (KRAS) G12C gene change. The goal of this study is to learn about the safety of MK-1084 and to learn how many people have the cancer get smaller or go away during the study treatment.

Conditions Studied

Interventions

  • BIOLOGICAL Pembrolizumab
  • DRUG Carboplatin
  • DRUG Pemetrexed
  • BIOLOGICAL Cetuximab
  • DRUG MK-1084

Study Locations (13)

Other

  • Severance Hospital Yonsei University Health System ( Site 0080) — Seoul
  • Hacettepe Universite Hastaneleri ( Site 0140) — Ankara
  • VISION PARTNER Medical Centre ( Site 0135) — Kyiv
  • LIMITED LIABILITY COMPANY "MEDICAL CENTER "DOBROBUT-CLINIC" ( Site 0138) — Kyiv

Florida

  • Clermont Oncology Center ( Site 0041) — Clermont

Overijssel

  • Deventer Ziekenhuis ( Site 0272) — Deventer

Cherkasy Oblast

  • COMMUNAL NONPROFIT ENTERPRISE CLINICAL CENTER OF ONCOLOGY, HEMATOLOGY, TRANSPLANTOLOGY AND PALLIATI ( Site 0139) — Cherkasy

Dnipropetrovsk Oblast

  • Medical Center "Mriya Med-Service"-Clinical Research Department ( Site 0465) — Kryvyi Rih

Ivano-Frankivsk Oblast

  • Communal Non-Commercial Enterprise "Prykarpatski Clinical On-Surgery department #2 ( Site 0132) — Ivano-Frankivsk

Kirovohrad Oblast

  • Limited Liability Company Ukrainian Center of Tomotherapy-Department of Chemotherapy ( Site 0467) — Kropyvnytskyi

Lviv Oblast

  • Lviv Territorial Medical Union Multidisciplinary Clinical Hospital ( Site 0133) — Lviv

Trial Details

FieldValue
Enrollment Target 130 participants
Start Date 2025-12-19
Est. Completion 2033-01-14
Phase Phase 2

Sponsor

Merck Sharp & Dohme

741 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07252739

The ClinicalTrials.gov registry entry for NCT07252739 describes a study currently listed as recruiting. It is categorized as Phase 2, 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 130 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Merck Sharp & Dohme, which has 741 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 Malignant Neoplasm 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: NCT07252739 reports 13 study locations spanning 10 distinct geographic areas — top geographies include Other, Florida, Overijssel. 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 NCT07252739 about?

NCT07252739 is a clinical study titled "KEYMAKER-U01 Substudy 01J: A Study of Pembrolizumab Plus MK-1084 in Participants With Non-Small Cell Lung Cancer (NSCLC) With Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS) G12C Mutations (MK-3475-01J/KEYMAKER-U01J)". Researchers want to learn if using a study medicine called MK-1084 can help treat NSCLC. MK-1084 is a type of treatment called targeted therapy for the Kirsten rat sarcoma viral oncogene homolog (KRAS) G12C gene change. The goal of this study is to learn about the safety of MK-1084 and to learn how ...

What is the current status of trial NCT07252739?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 130 participants. The study started on 2025-12-19. Estimated completion is 2033-01-14.

What conditions does trial NCT07252739 study?

This clinical trial studies the following conditions: Malignant Neoplasm. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07252739?

The interventions under investigation include: Pembrolizumab (BIOLOGICAL), Carboplatin (DRUG), Pemetrexed (DRUG), Cetuximab (BIOLOGICAL), MK-1084 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07252739?

This trial is sponsored by Merck Sharp & Dohme, which has 741 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07252739 being conducted?

This trial has 13 study locations across Florida, Overijssel, Cherkasy Oblast, Dnipropetrovsk Oblast, Ivano-Frankivsk Oblast. 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