Clin2
NCT05280509Possibly a fitRecruiting

Test TL-895 plus ruxolitinib for myelofibrosis

MyelofibrosisPrimary MyelofibrosisPost-PV MFPost-ET Myelofibrosis

Treatments studied

Part of Blood & lymphatic clinical trials.

This trial tests whether adding TL-895 to ruxolitinib can improve outcomes in adults with myelofibrosis. It focuses on people who are not getting enough benefit from ruxolitinib or who need treatment as part of the study.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1/Phase 2
Enrollment
70 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 or older and can give informed consent
  • You have a confirmed diagnosis of primary myelofibrosis or post–polycythemia vera/essential thrombocythemia myelofibrosis
  • If you are already on ruxolitinib, your dose must be stable before starting the study
  • Your risk level must be one of the study’s higher-risk groups (DIPSS low enough to include intermediate/high risk)
  • You have an enlarged spleen (either measured by scan/volume or felt as at least 5 cm below a chest landmark)
  • Your strength/mobility is good enough for study participation (ECOG 0 to 2)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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