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Active, not recruiting Phase 2 Interventional Results available

A Study of Participant Reported Preference for Subcutaneous Pembrolizumab Coformulated With Berahyaluronidase Alfa (MK-3475A) Over Intravenous Pembrolizumab (MK-3475) Formulation in Multiple Tumor Types (MK-3475A-F11)

ClinicalTrials.gov ID: NCT06099782

Public ClinicalTrials.gov record NCT06099782. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 7:44 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2 Study to Evaluate Patient Reported Preference for Subcutaneous Pembrolizumab Coformulated With Hyaluronidase (MK-3475A) Over Intravenous Pembrolizumab Formulation in Participants With Multiple Tumor Types (MK-3475A-F11)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate participant preference for coformulated hyaluronidase/pembrolizumab pembrolizumab (+) berahyaluronidase alfa \[MK-3475A\] administered subcutaneously (SC) over pembrolizumab \[MK-3475\] administered intravenously (IV) in participants with multiple tumor types. There will be no hypothesis testing in this study.

Study identification

NCT ID
NCT06099782
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
147 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 26, 2023 (Actual)
Primary completion
Apr 9, 2025 (Actual)
Completion
Feb 15, 2027 (Estimated)
Last update posted
Apr 8, 2026

2023 – 2027

United States locations

U.S. sites
8
U.S. states
7
U.S. cities
8
Facility City State ZIP Site status
Russell Medical ( Site 0160) Alexander City Alabama 35010 —
Alaska Oncology and Hematology ( Site 0121) Anchorage Alaska 99508 —
Highlands Oncology Group-Research Department ( Site 0133) Springdale Arkansas 72762 —
Marin Cancer Care ( Site 0148) Greenbrae California 94904 —
Holy Cross Hospital-Clinical Research ( Site 0159) Fort Lauderdale Florida 33308 —
Mid Florida Hematology and Oncology Center ( Site 0113) Orange City Florida 32763 —
Northwest Georgia Oncology Centers, a Service of Wellstar Cobb Hospital-Research ( Site 0112) Marietta Georgia 30060 —
Kadlec Clinic Hematology and Oncology ( Site 0103) Kennewick Washington 99336 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 37 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06099782, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 8, 2026 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06099782 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →