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Merck Sharp & Dohme LLC

Total Trials
21
Recruiting
21
Phases
Phase 3, Phase 1, Phase 2, Phase 2, Phase 3, Phase 1, Phase 2

Merck Sharp & Dohme LLC is the United States subsidiary of Merck & Co., Inc., one of the world's largest pharmaceutical companies by revenue and clinical trial activity. MSD — as the company is known outside the US — has been a driving force in vaccine development for over a century and more recently became central to the immune-oncology revolution through the development of pembrolizumab (Keytruda), now the world's top-selling cancer drug and the most widely studied oncology agent in clinical trial history.

Keytruda's clinical program alone spans hundreds of registered trials across 30+ cancer indications, encompassing first-line and later-line treatment, monotherapy, and combinations with chemotherapy, targeted agents, and bispecific antibodies. Beyond oncology, Merck's clinical portfolio includes antiviral programs (molnupiravir for COVID-19, HIV treatment research), cardiovascular disease, diabetes (sitagliptin/Januvia and successors), and vaccines including HPV (Gardasil 9), varicella, rotavirus, and investigational mRNA and subunit vaccines for respiratory viruses.

Merck-sponsored trials operate through the company's Global Clinical Trials organization and are conducted in partnership with academic centers, cooperative research networks, and industry research sites across more than 90 countries. Clinical data from MSD trials are submitted to regulatory agencies under strict FDA and EMA guidelines. Participants are monitored throughout enrollment by qualified clinical research coordinators at each trial site.

Frequently Asked Questions — Merck Sharp & Dohme LLC

What is pembrolizumab (Keytruda) and why is it in so many clinical trials?
Pembrolizumab is a PD-1 checkpoint inhibitor — a type of immunotherapy that blocks the PD-1 receptor on T cells, preventing cancer cells from suppressing the immune response. It was first approved by the FDA in 2014 for melanoma and has since been approved in over 30 cancer indications including lung, bladder, head and neck, colorectal, cervical, and many others. Because checkpoint inhibition works across tumor types defined by biomarkers rather than solely by tissue of origin, Merck has pursued one of the most expansive clinical trial programs in history — testing pembrolizumab alone and in combination with virtually every available cancer treatment modality. Trials range from Phase 1 dose-finding studies to large Phase 3 registration trials with thousands of participants.
What non-oncology clinical trials does Merck sponsor?
Merck's non-oncology trials span several major therapeutic areas. In infectious disease, MSD has an active antiviral pipeline and runs vaccine trials for emerging pathogens. In cardiometabolic disease, Merck sponsors trials on PCSK9 inhibition for LDL reduction (MK-0616) and investigational oral GLP-1 agents. Merck's neuroscience program includes trials on MK-0777 for cognition and investigational agents for neurodegeneration. The company also sponsors trials in animal health through its MSD Animal Health division — though these are separate from human study registration.
How can I find out if I qualify for a Merck clinical trial?
Merck operates a clinical trial finder at www.merck.com/clinical-trials/ where patients can search by disease, location, and age group. Each trial entry links to the full listing on ClinicalTrials.gov, which provides detailed eligibility criteria, trial site contacts, and the principal investigator's information. Patients interested in immunotherapy trials for cancer are advised to speak with their oncologist, who can assess whether PD-1/PD-L1 testing or other biomarker screening might qualify them for a Keytruda-based study.

Clinical Trials by Merck Sharp & Dohme LLC

NCT06623422 Phase 3
Recruiting

A Study of Pembrolizumab (MK-3475) With or Without Intismeran Autogene (V940) in Participants With Non-small Cell Lung Cancer (V940-009/INTerpath-009)

Carcinoma, Non-Small-Cell Lung
NCT06395103 Phase 1, Phase 2
Recruiting

Substudy 01A: Zilovertamab Vedotin in Pediatric and Young Adult Participants With Hematologic Malignancies or Solid Tumors (MK-9999-01A/LIGHTBEAM-U01)

B-cell Acute Lymphoblastic Leukemia
NCT07570173 Phase 2, Phase 3
Recruiting

A Clinical Trial of MK-1045 in People With B-cell Acute Lymphoblastic Leukemia (MK-1045-005)

B-cell Acute Lymphoblastic Leukemia
NCT07049926 Phase 1, Phase 2
Recruiting

Substudy 03C: A Study of Combination Therapies in Participants With Renal Cell Carcinoma With Recurrent Disease During or After Anti-PD-(L)1 Therapy (MK-3475-03C/KEYMAKER-U03)

Renal Cell Carcinoma
NCT07548606 Phase 1
Recruiting

A Drug-Drug Interaction Study of Itraconazole and Opevesostat (MK-5684) in Healthy Adult Male Participants (MK-5684-017)

Healthy
NCT07405164 Phase 3
Recruiting

Extension Study for Participants in Studies That Include Belzutifan (MK-6482-043/LITESPARK-043)

Von Hippel-Lindau Disease
NCT07030712 Phase 1
Recruiting

A Clinical Study of MK-8294 in Participants With Advanced Solid Tumors (MK-8294-001)

Metastatic Neoplasm
NCT06345729 Phase 3
Recruiting

A Study of Calderasib (MK-1084) Plus Pembrolizumab (MK-3475) in Participants With KRAS G12C Mutant Non-small Cell Lung Cancer (NSCLC) With Programmed Cell Death Ligand 1 (PD-L1) Tumor Proportion Score (TPS) ≥50% (MK-1084-004/KANDLELIT-004)

Non-small Cell Lung Cancer
NCT06136559 Phase 3
Recruiting

A Study of Nemtabrutinib (MK-1026) Versus Comparator (Investigator's Choice of Ibrutinib or Acalabrutinib) in First Line (1L) Chronic Lymphocytic Leukemia (CLL)/ Small Lymphocytic Lymphoma (SLL) (MK-1026-011/BELLWAVE-011)

Chronic Lymphocytic Leukemia
NCT07463183 Phase 2
Recruiting

A Study to Evaluate Efficacy and Safety of MK-8690 in Participants With Moderately to Severely Active Ulcerative Colitis (MK-8690-002)

Colitis Ulcerative
NCT06637423 Phase 1, Phase 2
Recruiting

A Clinical Study of Sacituzumab Tirumotecan (MK-2870) in Patients With Bladder Cancer (MK-2870-027)

Non-Muscle Invasive Bladder Cancer
NCT07058077 Phase 2, Phase 3
Recruiting

A Study of Enlicitide Decanoate (MK-0616, an Oral PCSK9 Inhibitor) in Children and Adolescents With Heterozygous Familial Hypercholesterolemia (MK-0616-029)

Heterozygous Familial Hypercholesterolemia (HeFH)
NCT07199465 Phase 1
Recruiting

A Clinical Study of Letermovir (MK-8228) in Children and Adolescents Who Receive a Kidney Transplant (KT) (MK-8228-077)

Cytomegalovirus Prophylaxis
NCT06651281 Phase 3
Recruiting

Extension Study of Long-term Safety and Efficacy of Tulisokibart in Participants With Crohn's Disease or Ulcerative Colitis (MK-7240-011)

Crohn Disease
NCT04665037 Phase 2
Recruiting

Posaconazole (MK-5592) Intravenous and Oral in Children (<2 Years) With Invasive Fungal Infection (MK-5592-127)

Invasive Fungal Infection
NCT06445972 Phase 1, Phase 2
Recruiting

Substudy 06D: Combination Therapies in Second Line (2L) Gastroesophageal Adenocarcinoma (MK-3475-06D/Keymaker-U06)

Gastroesophageal Junction
NCT06925737 Phase 3
Recruiting

A Clinical Study of Ifinatamab Deruxtecan (I-DXd) in People With Metastatic Prostate Cancer (MK-2400-001)

Prostate Cancer
NCT06428409 Phase 1, Phase 2
Recruiting

A Clinical Study of MK-2870 Alone or With Other Treatments to Treat Gastrointestinal Cancers (MK-9999-02A)

Colorectal Cancer
NCT07318558 Phase 3
Recruiting

A Clinical Trial of Sac-TMT in People With Non-HRD Positive Advanced Ovarian Cancer (MK-2870-021)

Ovarian Neoplasms
NCT07227402 Phase 3
Recruiting

A Clinical Study of Belzutifan and Zanzalintinib in People With Recurrent Kidney Cancer Following Adjuvant Therapy (MK-6482-033)

Renal Cell Carcinoma
NCT07060807 Phase 3
Recruiting

A Clinical Study of Patritumab Deruxtecan to Treat Breast Cancer (MK-1022-016)

Breast Neoplasms
ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology