MOMENTUM: momelotinib vs danazol in patients with myelofibrosis previously treated with JAKi who are symptomatic and anemic.


Journal

Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629

Informations de publication

Date de publication:
Apr 2021
Historique:
pubmed: 12 1 2021
medline: 6 11 2021
entrez: 11 1 2021
Statut: ppublish

Résumé

Hallmark features of myelofibrosis (MF) are cytopenias, constitutional symptoms and splenomegaly. Anemia and transfusion dependency are among the most important negative prognostic factors and are exacerbated by many JAK inhibitors (JAKi). Momelotinib (MMB) has been investigated in over 820 patients with MF and possesses a pharmacological and clinical profile differentiated from other JAKi by inhibition of JAK1, JAK2 and ACVR1. MMB is designed to address the complex drivers of iron-restricted anemia and chronic inflammation in MF and should improve constitutional symptoms and splenomegaly while maintaining or improving hemoglobin in JAKi-naive and previously JAKi-treated patients. The MOMENTUM Phase III study is designed to confirm and extend observations of safety and clinical activity of MMB. Lay abstract The most important features of myelofibrosis (MF) are low blood cell counts and symptoms including tiredness, night sweats and itching, along with increased size of the spleen, which may cause a feeling of fullness and pain. Low red blood cell counts (anemia) may mean regular blood transfusions are needed and this is one of the signs MF is getting worse. Drugs called JAK inhibitors (JAKi) are available to treat MF, but can have a side effect of making blood cell counts lower. Momelotinib (MMB) is a different type of JAKi to the ones currently available, and is an experimental drug for MF. MMB is designed to treat symptoms and spleen like other JAKi, but also to improve blood cell counts. MMB has already been given to more than 820 patients with MF in other clinical studies. Some of the patients in these studies had been treated with different JAKi before, and others got MMB as their first JAKi treatment. The MOMENTUM Phase III study is designed to collect more information on the safety and effectiveness of MMB in MF.

Autres résumés

Type: plain-language-summary (eng)
Lay abstract The most important features of myelofibrosis (MF) are low blood cell counts and symptoms including tiredness, night sweats and itching, along with increased size of the spleen, which may cause a feeling of fullness and pain. Low red blood cell counts (anemia) may mean regular blood transfusions are needed and this is one of the signs MF is getting worse. Drugs called JAK inhibitors (JAKi) are available to treat MF, but can have a side effect of making blood cell counts lower. Momelotinib (MMB) is a different type of JAKi to the ones currently available, and is an experimental drug for MF. MMB is designed to treat symptoms and spleen like other JAKi, but also to improve blood cell counts. MMB has already been given to more than 820 patients with MF in other clinical studies. Some of the patients in these studies had been treated with different JAKi before, and others got MMB as their first JAKi treatment. The MOMENTUM Phase III study is designed to collect more information on the safety and effectiveness of MMB in MF.

Identifiants

pubmed: 33423550
doi: 10.2217/fon-2020-1048
doi:

Substances chimiques

Benzamides 0
Janus Kinase Inhibitors 0
Pyrimidines 0
N-(cyanomethyl)-4-(2-((4-(4-morpholinyl)phenyl)amino)-4-pyrimidinyl)benzamide 6O01GMS00P
JAK1 protein, human EC 2.7.10.2
JAK2 protein, human EC 2.7.10.2
Janus Kinase 1 EC 2.7.10.2
Janus Kinase 2 EC 2.7.10.2
ACVR1 protein, human EC 2.7.11.30
Activin Receptors, Type I EC 2.7.11.30
Danazol N29QWW3BUO

Types de publication

Clinical Trial Protocol Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1449-1458

Subventions

Organisme : Sierra Oncology Ltd. (Sponsor)

Auteurs

Srdan Verstovsek (S)

Department of Leukemia at The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

Chih-Cheng Chen (CC)

Division of Hematology, Chang Gung Memorial Hospital, Chiayi, Taiwan.

Miklós Egyed (M)

Department of Hematology, Somogy County Mór Kaposi General Hospital, Kaposvár, 7400, Hungary.

Martin Ellis (M)

Hematology Institute & Blood Bank, Meir Medical Center, Kfar Saba & Sackler School of Medicine, Tel Aviv University, Tel Aviv, 6997801, Israel.

Laura Fox (L)

Department of Hematology, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Barcelona, 08035, Spain.

Yeow T Goh (YT)

Singapore General Hospital, 169608, Singapore.

Vikas Gupta (V)

Cancer Clinical Research Unit, Princess Margaret Cancer Centre, Toronto, ON, M5G 2C1, Canada.

Claire Harrison (C)

Guy's & St. Thomas' NHS Foundation Trust, London, SE1 9RS, UK.

Jean-Jacques Kiladjian (JJ)

Centre d'Investigations Cliniques (INSERM CIC 1427), AP-HP, Hopital Saint-Louis, Université de Paris, Paris, 75010, France.

Mihaela C Lazaroiu (MC)

Policlinica de Diagnostic Rapid Brasov, 500152, Romania.

Adam Mead (A)

Oxford University Hospitals NHS Foundation Trust, Oxford, OX3 9DU, UK.

Donal McLornan (D)

Guy's & Saint Thomas' NHS Foundation Trust, London, UK.

Mary F McMullin (MF)

Queen's University Belfast, Belfast, BT9 7BL, Ireland.

Stephen T Oh (ST)

Hematology Division, Washington University, St. Louis, MO 63110, USA.

Andrew Perkins (A)

The Alfred Hospital & Monash University, Melbourne 3004, Australia.

Uwe Platzbecker (U)

Leipzig University Hospital, Leipzig, 04103, Germany.

Christof Scheid (C)

Department of Internal Medicine & Center of Integrated Oncology Cologne Bonn, University of Cologne, Köln, 50923, Germany.

Alessandro Vannucchi (A)

Center Research & Innovation of Myeloproliferative Neoplasms, AOU Careggi, University of Florence, Firenze, 50139, Italy.

Sung-Soo Yoon (SS)

Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.

Mark M Kowalski (MM)

Sierra Oncology, Vancouver, BC, V6C 3E8, Canada.

Ruben A Mesa (RA)

Mays Cancer Center, UT Health San Antonio Cancer Center, San Antonio, TX 78229, USA.

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Classifications MeSH