Luspatercept + Pacritinib for Myelofibrosis
What You Need to Know Before You Apply
What is the purpose of this trial?
This study is for participants who have been diagnosed with myelofibrosis with cytopenia. Luspatercept and Pacritinib are experimental drug combination that works by blocking certain enzymes to calm an overactive inmmune system to reduce inflammation which would allow red blood cells to mature. The purpose of this study is to find out if the combination of Luspatercept and Pacritinib can help improve hemobglobin or transfusion dependents in participants with myelofibrosis with cytopenias.
Who Is on the Research Team?
Akriti Jain, MD, FACP
Principal Investigator
The Cleveland Clinic
Are You a Good Fit for This Trial?
This trial is for people with myelofibrosis who also have low blood counts, including anemia (low red cells) and thrombocytopenia (low platelets). Participants should not have other serious health issues that would prevent them from joining.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- Luspatercept
- Pacritinib
Trial Overview
The study tests a combination of two experimental drugs, Luspatercept and Pacritinib, to see if they can improve hemoglobin levels or reduce the need for blood transfusions in people with myelofibrosis and low blood counts.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Luspatercept will be given through subcutaneous injection on Day 1of each cycle at a starting dose of 1.33 milligrams/kilogram and can go up to a maximum dose of 1.75 milligrams/kilogram. Pacritinib will be given twice daily orally at a dose of 200 milligrams. Each cycle lasts 21 days.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Case Comprehensive Cancer Center
Lead Sponsor
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