Study Comparing Bomedemstat and Hydroxycarbamide for Patients with Essential Thrombocythemia

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What is this study about?

This clinical trial is focused on studying a condition called Essential Thrombocythemia, which is a type of blood disorder where the body produces too many platelets. Platelets are small blood cells that help with clotting, and having too many can lead to problems like blood clots or bleeding. The study is comparing two treatments: Bomedemstat, also known by its code name MK-3543, and Hydroxycarbamide, which is also known as Hydroxyurea. These medications are being tested to see how effective and safe they are for people who have not received any previous treatment to reduce their platelet count.

The purpose of the study is to compare the effectiveness of Bomedemstat to Hydroxycarbamide in managing Essential Thrombocythemia. Participants in the study will be randomly assigned to receive either Bomedemstat, Hydroxycarbamide, or a placebo. The study will last for a period of up to 36 months, during which participants will take the medication orally in the form of capsules. Throughout the study, participants will be monitored regularly to assess their response to the treatment and to check for any side effects.

This trial aims to provide valuable information on which treatment might be more beneficial for managing Essential Thrombocythemia. By participating, individuals contribute to research that could improve future treatment options for this condition. The study is designed to ensure the safety and well-being of all participants, with regular check-ups and assessments conducted by healthcare professionals.

1 joining the study

Upon joining the study, the participant is confirmed to have a diagnosis of essential thrombocythemia based on specific criteria. The participant must not have received any prior treatment for this condition.

2 randomization

The participant is randomly assigned to receive either bomedemstat (MK-3543) or hydroxyurea. This process is double-blind, meaning neither the participant nor the researchers know which treatment is being administered.

3 treatment administration

The participant takes the assigned medication orally in the form of a hard capsule. The specific dosage and frequency are determined by the study protocol and are followed throughout the trial.

4 monitoring and assessments

Regular monitoring is conducted to assess the participant’s response to the treatment. This includes evaluating the durable clinicohematologic response and other health indicators.

Participants are also assessed for any changes in symptoms and overall health status using specific forms and questionnaires.

5 completion of the study

The study is estimated to conclude by May 14, 2029. Upon completion, the participant’s overall health and response to the treatment are thoroughly evaluated.

Who Can Join the Study?

  • Must have a diagnosis of Essential Thrombocythemia (ET), which is a condition where the body makes too many blood cells called platelets, based on specific medical guidelines.
  • Must have a bone marrow fibrosis score of Grade 0 or Grade 1. This means the bone marrow, where blood cells are made, is in a healthy or slightly affected state.
  • Must not have received any previous treatment aimed at reducing blood cell production for their ET.
  • If the participant has HIV (a virus that affects the immune system), it must be well controlled with medication.
  • If the participant has tested positive for Hepatitis B (a liver infection), they must have been on treatment for at least 4 weeks and have no detectable virus in their blood.
  • If the participant has a history of Hepatitis C (another liver infection), the virus must not be detectable in their blood.
  • Both male and female participants are eligible to join the study.

Who Cannot Join the Study?

  • Patients with medical conditions other than Essential thrombocythemia cannot participate. Essential thrombocythemia is a condition where the body produces too many blood platelets, which are cells that help with blood clotting.
  • Patients who are not within the specified age range cannot participate. The age range includes adults and older adults.
  • Patients who are part of a vulnerable population cannot participate. A vulnerable population includes groups of people who may have a higher risk of harm or exploitation.

Where you can join this trial?

Verified and Recommended Sites

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Verified Sites

Other Sites

Site Name City Country Status
Karolinska University Hospital Solna Sweden
Centre Hospitalier Universitaire De Nice Nice France
Utkstzzuek On Dqiznfjo Debrecen Hungary
Hxzvounr Vraf dembavjc Barcelona Spain
Roktqs Sraipksen Holbæk Denmark
Oltbwg Uddrnpithr Hzqxknpa Odense Denmark
Fvtteelxow Imaip Cy Gcijzr Owqivjse Mmlrbptt Pwizjktxwyc Milan Italy
Fapecppoie Iwdwv Pyajuczjmpm Smr Mshfyc Pavia Italy
Adlabixmxc Prsmpwjd Hhyxtbrq Dh Mzndiqwjt Marseille France
Rtlgti Sjxcp Seehcq Uqvpcenliecwgoxqpoj Lund Sweden
Ujteuwl Uvttnuqyxr Hlvtsncj Uppsala Sweden
Hzstffmi Cgshdc Dn Beunqdaxk Barcelona Spain
Czjnnv Hqdnkujjred Rkwinejf Ucsqunnmcmvpt Dk Tbrhs Tours France
Rgrlvi Mvgszqgadas Aarhus Denmark
Ueaglhpsou Ob Sgaxps Szeged Hungary
Rerppvwnzvandr Copenhagen Denmark
Apultiv Uevqr Sjjznbpnb Lfqykk Dl Bmsbcag Bologna Italy
Ubwuuzzgvtmatbjwxiajn Ejuan Axt Essen Germany
Rltxlj Oclkayv Lros Orebro Sweden
Oazujatulphugs Lsfg Gluq Linz Austria
Uqzvsohbkdtjvvtddubmr Aqhdlb Alz Aachen Germany
Captto Hvywcudewej Lkhe Spb Pierre Benite France
Haygprhr Uiwqhgwxbohwe 1u Dh Ozynaim Madrid Spain
Hnvjgtyp Unrsqbiilabop Mqzoxdw Do Vmfhnrkeyj Santander Spain
Ixyggfyw Cnqctk Deoaojnonfqiynghr L'hospitalet De Llobregat Spain
Qvabl Slraea Crbtwzlgs Hbdssofe &sxcoel Stbphblpgxv Ulpbjjwzzo Hhgcnrsy &mrtole Vahbofq Gtztwejlbugzfciyso Gothenburg Sweden
Alaokyp Skjgq Stfddzsdg Taxiqkskqfnq Ddq Smuox Lgamy Varese Italy
Pouppe Hyoxnmevyyl Saj z ooor Katowice Poland
Sxpdwb Vbvmvizdg Klxnkf Mwe Ofwfzq Kdmggh Kaposvar Hungary
Iraknbmts Dt Irhzmpctmqafp Ek Cdlikkfs Dv Lx Sgsxx Gqzjojh Tgpnz I Pwabc Barcelona Spain
Ancmehhwmc Ppmqaxay Hfykdfly Ds Pmnma Paris France
Sjzvxctkwqjmhmauvksvah Vaihhdivv Oiccozwrwizn Nyiregyhaza Hungary
Gkwygbousqagzgsga Vaimqpcdj Pbqf Aefdzd Ezlnjmxt Omfhxp Khjygt Gyor Hungary
Azcgsjv Ocvdqhuvxxl Nslcwadrw Sy Abplusj E Buqwhx E C Aezibs Alpykcjdjbr Alexandria Italy
Sbgtvusddqy Pejvtgjij Sdfjhje Kabdbntnw Nz 1 W Ltrchuqt Lublin Poland
Dhf Vrntxvwsavmynp Mcn Gglz Landshut Germany
Sqijfddzczofko Cenyxau Opdgxvfvq Szoozdqddge Pxemjsvgz Zjxjho Owvium Znsxlzeuvw W Kcmmyocw Kielce Poland
Mpyuvqgllwgouapczvyqpnjbbk Hhiqxtsayxpwozhw Halle (Saale) Germany
Hqupftng Cksgz dxb Swa Marbella Spain

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
07.10.2024
Denmark Denmark
Not recruiting
07.10.2024
France France
Not recruiting
07.10.2024
Germany Germany
Not recruiting
07.10.2024
Hungary Hungary
Not recruiting
07.10.2024
Italy Italy
Not recruiting
07.10.2024
Poland Poland
Not recruiting
07.10.2024
Spain Spain
Not recruiting
07.10.2024
Sweden Sweden
Not recruiting
07.10.2024

Trial locations

Bomedemstat (MK-3543) is a medication being studied for its effectiveness and safety in treating essential thrombocythemia, a condition characterized by an overproduction of platelets in the blood. This medication is being compared to another treatment to see how well it works in managing the disease.

Hydroxyurea is a medication commonly used to treat essential thrombocythemia. It helps to reduce the number of platelets in the blood, which can help prevent complications associated with the condition. In this study, it serves as a comparison to evaluate the effectiveness of bomedemstat.

Investigated Diseases:

Essential thrombocythemia – This is a chronic blood disorder characterized by the overproduction of platelets by the bone marrow. It often progresses slowly and may not cause symptoms initially. Over time, individuals may experience headaches, dizziness, or vision changes due to increased blood viscosity. Some people may also develop blood clots or bleeding issues. The condition can lead to complications such as an enlarged spleen or changes in blood cell counts. It is considered a type of myeloproliferative neoplasm, which involves the abnormal growth of blood cell precursors.

Trial ID:
2023-505232-36-00
Protocol code:
MK-3543-007
Trial Phase:
Therapeutic confirmatory (Phase III)

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