Clinical trial

Relative Bioavailability Study of Subcutaneous Injection Versus Intravenous…

NCT03665597 · Merck Sharp & Dohme LLC, Industry · Completed

Key facts

NCT number NCT03665597
Title Relative Bioavailability Study of Subcutaneous Injection Versus Intravenous Infusion of Pembrolizumab (MK-3475) in Participants With Advanced Melanoma (MK-3475-555/KEYNOTE-555)
Official title A Phase 1 Randomized Clinical Study of Pembrolizumab (MK-3475) to Evaluate the Relative Bioavailability of Subcutaneous Injection Versus Intravenous Infusion in Participants With Advanced Melanoma (KEYNOTE-555)
Lead sponsor Merck Sharp & Dohme LLC, Industry
Status Completed
Phase Phase 1
Study type Interventional
Conditions Melanoma
Intervention type Biological
Interventions Pembrolizumab Dose C, Pembrolizumab Dose A, Pembrolizumab Dose B, Pembrolizumab Dose D
Enrollment 138
Start date Nov 19, 2018
Primary completion Dec 4, 2023
Completion Dec 4, 2023
First posted Sep 11, 2018
Last update posted Feb 10, 2025
Countries Australia, South Africa, Spain, Sweden

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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