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Study identifier: NCT05037760 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study of Elritercept Alone or Together With Ruxolitinib in Adults With Myelofibrosis

Condition: Myelofibrosis  ·  Sponsor: Takeda

PhasePhase 2
Planned participants135
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The main aim of this study is to learn how safe elritercept is and how well it is tolerated when taken alone and in combination with the JAK inhibitor, ruxolitinib. Other aims are to learn about the effects of elritercept on the signs and symptoms of MF when taken with or without ruxolitinib and to learn how elritercept affects the body, how the body processes elritercept, and the effects of elritercept on anemia when taken with or without ruxolitinib The study will also check on how safe elritercept is and how well it is tolerated.

This description comes directly from the study's public registry record.

Talk to the study team

Takeda Contact  ·  +1-877-825-3327  ·  medinfoUS@takeda.com

Always discuss trial participation with your own doctor first.

Locations (46)

Concord HospitalConcord, New South Wales, AustraliaRecruiting
The Tweed HospitalTweed Heads, New South Wales, AustraliaRecruiting
Flinders Medical CentreWoodville South, South Australia, AustraliaRecruiting
St. Vincents Hospital MelbourneFitzroy, Victoria, AustraliaRecruiting
Royal Melbourne HospitalMelbourne, Victoria, AustraliaRecruiting
Ballarat Oncology & Haematology ServiceWendouree, Victoria, AustraliaRecruiting
Hospital de Clinicas de Porto AlegrePorto Alegre, BrazilRecruiting
IMV-Pesquisa Cardiologica Sociedade SimplesPorto Alegre, BrazilRecruiting
Albert Einstein Sociedade Beneficente Israelita BrasilieraSão Paulo, BrazilRecruiting
Hospital Beneficencia Portuguesa de Sao PauloSão Paulo, BrazilRecruiting
Hospital Das Clinicas Da Faculdade de Medicina Da U S PSão Paulo, BrazilRecruiting
Instituto de Ensino e Pesquisas Sao LucasSão Paulo, BrazilRecruiting

+ 34 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05037760