RecruitingPhase 2NCT06986174

A Phase 2 Study to Evaluate the Safety and Efficacy of Pacritinib in Relapsed or Refractory Waldenström Macroglobulinemia


Sponsor

Shayna Sarosiek, MD

Enrollment

30 participants

Start Date

Nov 21, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This study is being done to examine the safety and effectiveness of pacritinib as a possible treatment for participants with Waldenström macroglobulinemia (WM). The name of the study drug involved in this study is: -Pacritinib (a type of kinase inhibitor)


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This Phase 2 study is testing whether a drug called pacritinib can safely and effectively treat Waldenström macroglobulinemia — a rare type of slow-growing blood cancer — in patients whose cancer came back or stopped responding to previous treatments. **You may be eligible if...** - You are 18 or older - You have a confirmed diagnosis of Waldenström macroglobulinemia - Your cancer has returned or stopped responding to prior treatment - You have symptoms requiring treatment (e.g., fatigue, night sweats, low blood counts, swollen lymph nodes, or other complications) - Your IgM protein level is at least twice the upper limit of normal - Your overall health and organ function meet study requirements **You may NOT be eligible if...** - You have not had prior treatment, or your disease is not yet symptomatic - Your organ function does not meet minimum requirements - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPacritinib

Kinase inhibitor, capsule, taken orally per protocol.


Locations(1)

Dana Farber Cancer Institute

Boston, Massachusetts, United States

View Full Details on ClinicalTrials.gov

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NCT06986174


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