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RecruitingLast updated:15 August 2023

This phase I trial is evaluating the safety and effectiveness of increasing doses of an immunotherapy drug (MK-1308) given in combination with another immunotherapy drug (Pembrolizumab) for the treatment of patients with advanced solid tumoursA Phase 1 Open Label, Multi-Arm, Multicenter Study of MK-1308 in Combination With Pembrolizumab for Subjects With Advanced Solid Tumors

Clinical summary

Summary

Participants eligible for this trial will be assigned to either a Dose Escalation or Dose Confirmation phase of the trial. Patients in the Dose Escalation phase of the trial will receive MK-1308 on Day 1 of the first cycle, MK-1308 and pembrolizumab of Day 1 of cycles 2-5 and pembrolizumab for on Day 1 of the remaining cycles. Patients in the Dose Confirmation phase of the trial will receive MK-1803 and pembrolizumab on Day 1 of all cycles. Patients in both trial phases will be treated for up to 35 cycles.

Age

People18+

Phase

I

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Trial Identifiers

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Commercial Sponsor

Merck

Scientific Title

A Phase 1 Open Label, Multi-Arm, Multicenter Study of MK-1308 in Combination With Pembrolizumab for Subjects With Advanced Solid Tumors

Eligibility

Inclusion

  • You have certain types of non-cancer medical conditions.
  • You have been diagnosed with a prior or secondary type of cancer.
  • You have had certain treatments, surgical procedures or drugs.
Message

Clinical trials have complex eligibility criteria.

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