Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • B-cell Non Hodgkin Lymphoma
  • Follicular Lymphoma
  • Indolent Non Hodgkin Lymphoma
  • Marginal Zone Lymphoma
Type
Interventional
Phase
Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

OUTLINE: Patients receive pembrolizumab intravenously (IV) over 30 minutes on day 1. Treatment repeats every 3 weeks for up to 18 cycles in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up for 30 days and then up to 5 years.

OUTLINE: Patients receive pembrolizumab intravenously (IV) over 30 minutes on day 1. Treatment repeats every 3 weeks for up to 18 cycles in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up for 30 days and then up to 5 years.

Tracking Information

NCT #
NCT03498612
Collaborators
  • National Cancer Institute (NCI)
  • Merck Sharp & Dohme Corp.
Investigators
Principal Investigator: Ajay K. Gopal Fred Hutch/University of Washington Cancer Consortium