Overview

A Study to Evaluate the Bioavailability of Pembrolizumab (MK-3475) Via Subcutaneous (SC) Injection of MK-3475A (Pembrolizumab Formulated With MK-5180) In Advanced Solid Tumors (MK-3475A-C18)

Status:
Recruiting
Trial end date:
2024-10-18
Target enrollment:
Participant gender:
Summary
This is a study to assess the pharmacokinetics, safety, and tolerability of pembrolizumab formulated with MK-5180 when administered as a SC injection to participants with advanced solid tumors. Participants will receive SC injections of MK-3475A containing one of 2 different concentrations (Conc) of pembrolizumab, Conc1 and Conc2, which total the same overall dose of pembrolizumab (Dose Level [DL] 1).
Phase:
Phase 1
Details
Lead Sponsor:
Merck Sharp & Dohme Corp.
Treatments:
Albumin-Bound Paclitaxel
Axitinib
Carboplatin
Paclitaxel
Pembrolizumab
Pemetrexed