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Clinical Trials in Canada / NCT05853367
Active, not recruiting Phase 1

Study of MK-0472 in Participants With Advanced/Metastatic Solid Tumors (MK-0472-001)

NCT05853367 · tracked via the Priya Life Science Canada tracker
Phase
Phase 1
Started
2023-07-06
Last updated
2026-08-07

Condition(s) studied

Metastatic Solid TumorsAdvanced Solid Tumors

Investigational drug(s) / intervention(s)

MK-0472Pembrolizumab →MK-1084 →

MK-0472: Oral Administration

Pembrolizumab: IV infusion

MK-1084: Oral Administration

Study summary

The purpose of this study is to assess the efficacy, safety, and tolerability of MK-0472 administered as monotherapy and in combination with pembrolizumab (MK-3475) or MK-1084 in participants with histologically or cytologically confirmed diagnosis of advanced/metastatic solid tumors.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: The main inclusion criteria include but are not limited to the following: * Has histologically or cytologically confirmed solid tumor by pathology report that is advanced/metastatic * Participants who are hepatitis B surface antigen (HBsAg) positive are eligible if they have received HBV antiviral therapy for at least 4 weeks, and have undetectable HBV viral load prior to study enrollment * Participants with history of hepatitis C virus (HCV) infection are eligible if HCV viral load is undetectable at screening * Participants with human immunodeficiency virus (HIV) infection must have well controlled HIV on stable (\>4 weeks) antiretroviral therapy (ART) * Arm 1: Oncogenic receptor tyrosine kinase (RTK) pathway alterations confirmed by a historical report or local testing (tissue or blood) and have received, or been intolerant to, all available treatment known to confer clinical benefit * Arm 2: Tumor types known to be sensitive to anti-programmed cell death 1 protein (PD-1)/ligand 1 (L1) therapies are eligible. Tumor types permitted include: melanoma, non-small cell lung cancer (NSCLC) without epidermal growth factor receptor (EGFR)/anaplastic lymphoma kinase (ALK)/ROS1 mutations, renal cell carcinoma, urothelial carcinoma, Merkel cell carcinoma, MSI-high CRC, endometrial cancer, cervical cancer, small cell lung cancer, triple negative breast cancer, esophageal cancer, gastric cancer, biliary tract cancer, hepatocellular carcinoma, head and neck squamous cancer, cutaneous squamous cancer, anal squamous cancer, and mesothelioma * Arm 3: Has histologically OR blood-based confirmation of Kirsten rat sarcoma viral oncogene homolog (KRAS) G12C mutation Exclusion Criteria: The main exclusion criteria include but are not limited to the following: * Has not recovered to common terminology criteria for adverse events (CTCAE) Grade 1 or better from any adverse events that were due to cancer therapeutics administered more than 4 weeks earlier. Participants receiving ongoing replacement hormone therapy for endocrine immune-related AEs will not be excluded from participation in this study * Has history of a second malignancy, unless potentially curative treatment has been completed with no evidence of malignancy for 2 years * History of hyperparathyroidism or hypercalcemia * Has one or more of the following ophthalmological findings/conditions: a) Intraocular pressure \>21 mm Hg and/or any diagnosis of glaucoma b) Diagnosis of central serous retinopathy, retinal vein occlusion, or retinal artery occlusion and c) Diagnosis of retinal degenerative disease * Has clinically significant cardiovascular disease * Bullous exfoliative skin disorders of any grade * Known hypersensitivity to MK-0472, MK-1084, or pembrolizumab, or any of their excipients * Received therapy with a proton-pump inhibitor or an H2 histamine blocker receptor antagonist within 7 days before the first scheduled day of study dosing * Has discontinued prior therapy with an anti-programmed cell death-1 (PD-1), anti-programmed death-ligand 1 (PD-L1), or anti-programmed death-ligand 2 (PD-L2) agent or with an agent directed to another stimulatory or coinhibitory T-cell receptor due to an adverse event * Received prior systemic anticancer therapy including investigational agents within 4 weeks before first dose * Received a live or live-attenuated vaccine within 30 days before the first dose of study intervention * Has received an investigational agent or has used an investigational device within 4 weeks prior to study intervention administration * Has diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of study medication * Has known additional malignancy that is progressing or has required active treatment within the past 2 years * Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis. Participants with previously treated brain metastases may participate provided they are radiologically stable for at least 4 weeks as confirmed by repeat imaging performed during the study screening, are clinically stable and have not required steroid treatment for at least 14 days before the first dose of study intervention * Has active autoimmune disease that has required systemic treatment in the past 2 years except replacement therapy * Has history of pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease * Has active infection requiring systemic therapy * Has history of allogeneic tissue/solid organ transplant * Have not adequately recovered from major surgery or have ongoing surgical complications

Primary outcome measure(s)

Trial sites (25)

FacilityCityRegionStatus
Northwestern Memorial Hospital ( Site 0002) Chicago Illinois
The University of Louisville, James Graham Brown Cancer Center ( Site 0004) Louisville Kentucky
John Theurer Cancer Center at Hackensack University Medical Center ( Site 0001) Hackensack New Jersey
Rutgers Cancer Institute of New Jersey ( Site 0005) New Brunswick New Jersey
Princess Margaret Cancer Centre ( Site 0101) Toronto Ontario
Centre Hospitalier de l'Université de Montréal-Unit for Innovative Therapies ( Site 0100) Montreal Quebec
Département clinique de médecine de laboratoire du CHUM ( Site 0104) Montreal Quebec
Centro de Estudios Clínicos SAGA ( Site 0701) Santiago Region M. de Santiago
Fundacion Arturo Lopez Perez ( Site 0700) Santiago Region M. de Santiago
Centro de Investigacion Clinicadela Universidad Catolica ( Site 0703) Santiago Region M. de Santiago
Bradfordhill ( Site 0702) Santiago Region M. de Santiago
Rambam Health Care Campus ( Site 0304) Haifa Israel
Shaare Zedek Medical Center ( Site 0303) Jerusalem Israel
Rabin Medical Center ( Site 0301) Petah Tikva Israel
Sheba Medical Center ( Site 0300) Ramat Gan Israel
Sourasky Medical Center ( Site 0302) Tel Aviv Israel
Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie - Panstwowy Instytut Badawczy w Warszawie ( Site 0401) Warsaw Masovian Voivodeship
Uniwersyteckie Centrum Kliniczne ( Site 0400) Gdansk Pomeranian Voivodeship
Institut Català d'Oncologia - L'Hospitalet-Medical Oncology ( Site 0501) L'Hospitalet de Llobregat Catalonia
Centro Integral Oncologico Clara Campal-Hospital HM Universitario Sanchinarro-START Madrid, ( Site 0504) Madrid Madrid, Comunidad de
Hospital Universitari Vall d'Hebron ( Site 0500) Barcelona Spain
Hospital Virgen del Rocio ( Site 0503) Seville Spain
Hôpitaux Universitaires de Genève (HUG) ( Site 0202) Geneva Canton of Geneva
Cantonal Hospital St.Gallen-Oncology & Hematology ( Site 0201) Sankt Gallen Canton of St. Gallen
Ospedale Regionale Bellinzona e Valli ( Site 0200) Bellinzona Canton Ticino

On this site

📄 Keytruda (pembrolizumab) drug profile →

More Merck Sharp & Dohme LLC trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05853367 on ClinicalTrials.gov ↗ ← All trials in Canada