CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 10 enrolled
Drug / intervention
Pembrolizumabdrug
Likely dose
Pembrolizumab 200 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03065400
NCT03065400Phase 2Completed

PD-1 Inhibition in Advanced Myeloproliferative Neoplasms

John Mascarenhas·interventional·Posted Feb 27, 2017·Updated Jun 21, 2021

In Brief

A Phase 2 clinical trial evaluating Pembrolizumab for Chronic Phase Myelofibrosis and 3 related conditions. Completed, enrolled 10 participants across 3 sites.

Detailed Summary

The purpose of this study is to test the effectiveness of a drug called pembrolizumab in patients with Myeloproliferative Neoplasm (MPN); chronic phase (MF-CP), accelerated phase (MPN-AP), or blast phase (MF-BP). Myelofibrosis neoplasm (MPN) is a group of diseases of the bone marrow in which excessive cells are produced. Pembrolizumab also known as Keytruda is a drug that has recently been approved in the United Stated by the Food and Drug Administration (FDA) for the treatment of patients with unresectable or metastatic melanoma and disease progression. Pembrolizumab is experimental in the treatment of MPN. The researchers want to find out what effects, good and /or bad it has on participants and the disease. Participants qualify to take part in this research study if have been diagnosed with a MPN blood disorder called myelofibrosis (MF). Accelerated (10-19% blasts in the blood or bone marrow) and blast phase (\>20% blasts in the blood or bone marrow) MPN has been a difficult disease to treat. The term "blasts" refers to immature cells found in the bone marrow. They are not fully developed, and therefore, do not yet carry out any particular function within the body. Funds for conducting this research are provided by Merck and Company, the manufacturer of the study drug pembrolizumab.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedFeb 27, 2017
Enrollment StartJun 14, 2017
Primary CompletionMay 28, 2020
TodayJul 2, 2026
Enrollment to primary: 3.0 yearsPosted 9.3 years ago

Interventions

Pembrolizumabdrug

200 mg of Pembolizumab administered via intravenous infusion over 30 mins given every 3 weeks