A study of bleximenib combined with intensive chemotherapy for adults with newly diagnosed acute myeloid leukemia with specific genetic changes.

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What is this study about?

This study involves patients with Acute Myeloid Leukemia, a type of blood cancer that affects the bone marrow and blood. The study focuses on patients whose leukemia has specific genetic changes, either a change in a gene called NPM1 or rearrangements involving a gene called KMT2A. The treatment being tested is JNJ-75276617, also known as bleximenib, which is given in the form of film-coated tablets taken by mouth. Some patients will receive bleximenib while others will receive placebo.

The purpose of this study is to find out if adding bleximenib to the standard intensive chemotherapy treatment can help patients live longer without their disease getting worse compared to receiving standard chemotherapy with placebo. The standard treatment includes chemotherapy to put the disease into remission, followed by additional chemotherapy to strengthen this response, and then maintenance therapy to help keep the disease under control.

During the study, patients will receive either bleximenib or placebo together with their regular intensive chemotherapy treatment. The study follows patients through the initial treatment phase aimed at achieving remission, a consolidation phase to reinforce the response, and then a maintenance phase. Neither the patients nor their doctors will know whether they are receiving bleximenib or placebo during the study. The study will monitor how well the treatment works and track patient outcomes over time.

1 Randomization and treatment assignment

At the beginning of the study, you will be randomly assigned to receive either bleximenib or placebo. A placebo is an inactive substance that looks like the actual medication but contains no active ingredient.

Neither you nor your doctor will know which treatment you are receiving. This is called a double-blind study design.

The study medication will be given as film-coated tablets taken by mouth.

2 Remission induction chemotherapy phase

You will receive intensive chemotherapy aimed at achieving complete remission. Complete remission means that the leukemia cells are no longer detectable in your blood and bone marrow.

During this phase, you will also receive either bleximenib tablets or placebo tablets in combination with the chemotherapy.

The study medication (bleximenib or placebo) will be available in two strengths: 50 mg and 100 mg tablets.

3 Consolidation chemotherapy phase

After achieving complete remission, you will receive consolidation chemotherapy. This treatment is designed to eliminate any remaining leukemia cells and reduce the risk of the disease returning.

You will continue taking either bleximenib tablets or placebo tablets along with the consolidation chemotherapy.

4 Maintenance therapy phase

Following the completion of consolidation chemotherapy, you will enter the maintenance therapy phase.

During this phase, you will continue taking either bleximenib tablets or placebo tablets by mouth.

The purpose of maintenance therapy is to help prevent the leukemia from returning.

5 Monitoring and assessments

Throughout all phases of the study, your health will be closely monitored through regular medical examinations, blood tests, and bone marrow assessments.

Your kidney and liver function will be checked to ensure they are working adequately.

Your white blood cell count will be monitored. White blood cells are cells in your blood that help fight infections.

Your doctor will assess your overall physical condition using the WHO/ECOG performance status, which is a scale that measures how the disease affects your daily living abilities.

Who Can Join the Study?

  • You must be 18 years of age or older at the time you agree to join the study
  • You must have a new diagnosis of Acute Myeloid Leukemia, which is a type of blood cancer where abnormal white blood cells grow rapidly in the bone marrow. Your disease must show at least 10% blasts (immature blood cells) in your bone marrow (the soft tissue inside bones where blood cells are made) or blood
  • Your leukemia must have specific genetic changes: either a mutation in the NPM1 gene (a change in a specific gene) or rearrangements involving the KMT2A gene (changes in the structure of another specific gene)
  • Your doctor must determine that you are healthy enough to receive intensive chemotherapy, which is strong cancer treatment given through the vein
  • Your performance status must be 2 or less on the WHO/ECOG scale, which means you are able to care for yourself and are up and about for at least half of your waking hours
  • Your kidneys and liver must be working well enough before you are assigned to a treatment group
  • Your white blood cell count (the number of infection-fighting cells in your blood) must be less than 25 times 10 to the power of 9 per liter

Who Cannot Join the Study?

  • The source data does not provide specific exclusion criteria for this clinical trial
  • Exclusion criteria are reasons why a person cannot take part in a study, but these details were not included in the available information
  • This trial is studying a treatment called bleximenib for adults with a specific type of blood cancer called Acute Myeloid Leukemia, which is a cancer that affects blood cells and bone marrow
  • The study focuses on patients who have certain genetic changes in their cancer cells, specifically NPM1 mutation or KMT2A rearrangement, which are specific abnormalities in the cancer cells
  • Participants must be suitable for intensive chemotherapy, which means strong cancer-fighting medications given in high doses

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
University Hospital Jena KöR Jena Germany
Center For Pediatric And Adolescent Medicine Of The Johannes Gutenberg University Mainz Mainz Germany
Azienda Ospedaliero Universitaria Careggi Florence Italy
Technische Universitaet Dresden Dresden Germany
Katholieke Universiteit te Leuven Leuven Belgium
Oslo Universitetssykehus HF Oslo Norway
Medizinische Hochschule Hannover Hanover Germany
Frisius Heerenveen The Netherlands
University Medicine Greifswald Greifswald Germany
Rostock University Medical Center Rostock Germany
Uniwersytecki Szpital Kliniczny Im Jana Mikulicza Radeckiego We Wroclawiu Wroclaw Poland
Stichting OLVG Amsterdam The Netherlands

Other Sites

Site Name City Country Status
Karolinska University Hospital Solna Sweden
Helios Universitaetsklinikum Wuppertal Wuppertal Germany
Rheinische Friedrich-Wilhelms-Universitaet Bonn Bonn Germany
Hospital General Universitario Gregorio Maranon Madrid Spain
Hospital Del Mar Barcelona Spain
Amphia Hospital Breda The Netherlands
Otto Von Guericke Universitaet Magdeburg Magdeburg Germany
Universitätsklinikum des Saarlandes – Homburg/Saar, Klinik für Urologie und Kinderurologie Homburg Germany
Az St-Jan Brugge-Oostende A.V. Brugge Belgium
St. Antonius Ziekenhuis Nieuwegein The Netherlands
Hospital Son Llatzer Palma Spain
CHU Helora La Louviere Belgium
Cochutjho Uhobkvrofvkrzr Sgryhyckk Woluwe-Saint-Lambert Belgium
Kjfmkesd Nmbfqsdfu Nürnberg Germany
Hnbs Hvbytjfu Hague The Netherlands
Uufjmrjahxcorngntngud Nbwxudicii Hu Tromsø Norway
Iqlqlstz Jaxfs Baksqb Anderlecht Belgium
Nkexf Eufecgl Mwioepg Cozhpa Fuvwhxdvot Tallin Estonia
Bapoivxl Hvuqydbg Dublin Ireland
Ovthcd Uxpjooeiwi Hspiszvd Odense Denmark
Unxvsxkevxtwxjgswvpia Eisfkovz Aan Erlangen Germany
Fakeftkfug Iobkh Cp Grgjit Ocmiiyqp Mkapyidw Pzrhtkaucum Milan Italy
Acrn Gvhstm Ogghpljr Mhxobeqqslvoy Nltmogzh Milan Italy
Ahlakuigr Uof Amsterdam The Netherlands
Rdmqok Snofr Spcawm Uijljwzvifjfbhgkndd Lund Sweden
Uqzfblqezedx Mbzrqfn Ctfsrao Ukwfagf Utrecht The Netherlands
Uhyoczo Uvadmbpvuw Hvazgjtv Uppsala Sweden
Hjxbxxor Cvhfcn De Boayllewn Barcelona Spain
Hsuvo Batplk Hg Bergen Norway
Cnsezbv Uiwxnxbwrictpzxsixia Bgpius Kvu Berlin Germany
Vmvjmooz uimkypstnvew lltkpsgj Scqhuxsv kyoxcjwk Vhq Vilnius Lithuania
Urtrxoumcklvspimjdrku Dzddfvwintu Alb Duesseldorf Germany
Slqlfnrxwxjs Hofjwknfe Gank Heilbronn Germany
Pyidhfceuynldncjuipye Myvgutq Marburg Germany
Kosmyupm Ctgangaf grfok Chemnitz Germany
Heurpopr Uqdyarerru Cjenamr Hnbuytph Helsinki Finland
Evgodkm Uvrkbjorqndx Malitsa Cnczbpe Rsqirhfah (xhsicbp Mpi Rotterdam The Netherlands
Smmdwvgxq Rytfoit Uwucdukbey Mlenghl Ctzqno Nijmegen The Netherlands
Iypim Odvemnzg Pczvgoqzrpy Sta Mkludlw Genoa Italy
Hhndfxn Kyhqxhgpdpi Dao Wjdpag Gghehumeimxfntovlvt Vienna Austria
Uwdujhwezwlupckct Ptehifsijqm Difyd Mmrzli Ancona Italy
Aagkrnn Uigntwjrtv Hkdxxndf Aalborg Denmark
Joffp Zdknuyutpu Hasselt Belgium
Gvrgcnlotreciky Aakmyjazr Antwerp Belgium
Uioxummdaaecqdpleddfn Hicngtcqqi Aaw Heidelberg Germany
Mzhzdag Cyixpn &wyaiok Ukjxmofqrh Ov Fnosnezo Freiburg Im Breisgau Germany
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Rinybr Menkgwukvws Aarhus Denmark
Umatpdpsjq Hdxuamdu Mfuaonpapd Maastricht The Netherlands
Rjgwklcebhzndo Copenhagen Denmark
Ujszqmyspbpqvv Clkjeto Kbxhwddfm Gdansk Poland
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Sx Vojlegfxwxvhkfu Uccarhwfia Hkhcpgmi Dublin Ireland
Ukgsjvywjs Ot Amswpus Edegem Belgium
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Uaokyisega Mqfhgda Cgfozw Hrhdhjndctnttdlqp Hamburg Germany
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Ucepalkbzm Dqcca Soffd Du Rapd Lt Sfhmhjob Rome Italy
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Uphamnsfthrv Zesetficoj Gshp Gent Belgium
Ulgilcugjibh Mcrfcgj Cyjckle Gfhejbkwc Groningen The Netherlands
Usppkxamnfubvlwfcodna Abhqbi Afm Aachen Germany
Hgasw Sbncozisl Hm Stavanger Norway
Iimrvvag Cpiqzb Dqqglzpvvkxtunyls L'hospitalet De Llobregat Spain
Sfnwiu Dk Sgmrk Dh Low Izaeq Bhunkbh Palma Spain
Qvpsv Sfgfyv Cpiiprbey Hqrfggcb &fxdvgk Sirwxvppvha Ucxwzfgqua Hrnpmwai &lftcdo Vymmmat Gydmaboexcmmkirjqw Gothenburg Sweden
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Vbdxxpyksxislgyw hitmtcmticjtdvl Turku Finland
Pzpjpwuuhskcskehcd hronweiwyiadgtp Oulu Finland
Uucrblvrjudekgutrgkju Rejbjazbcj Azf Regensburg Germany
Kiknnfzb Dlr Loungdpgsmkgspne Sabpevktu goowk Stuttgart Germany
Tscex Uorwhnwaem Hguhzdvq Tartu Estonia
Vgsvudmmveth Ktvdtrkunfnhmkuqufcgrmkdcunqozjq msk Feldkirch Austria
Uxzfqsdqdv Hknxqbzl Gnfbfy Galway Ireland
Mxxbpxs Mgsxxhs Czotab Amersfoort The Netherlands
Hoqhqeuo Uozloictbqzr Acahm Da Vumwiwhp Df Lh Gsoglnhg Tobgzscdtoz Dw Lfmaqv Lleida Spain
Czv Mahhmccyy Liege Belgium
Gerlzn Ucxjwigspz Fmqzcnbtg Frankfurt Germany
Fkzhhgkq Alayxsjgeohi Dd Mxoqw Dc Tverzodi Fyu Terrassa Spain
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Piidmpyvpp hwpbdtihrwlqxxq Tampere Finland
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Sbgwugciziji Kuvbmfji Krvpwaoxt gtuhc Karlsruhe Germany
Ruwkqhkrz Zqstearikp Svieogudy Arnhem The Netherlands
Ibnvf Kvqtyqvtn Skovjnoug Zwolle The Netherlands
Vnuxvnxo Npmpbgwh fmyt Ggweqykawp Gltv Berlin Germany
Kddacpzt dph Sfgac Llocabkofsfz ao Rjcjc gsleg Ludwigshafen Am Rhein Germany
Mkjbjemhzguspadxrgsnoodagn Hjnuhbqbjyulttoy Halle (Saale) Germany
Azqdjycwz Kguoom Sa Gwujex Hamburg Germany
Hfzibxey Szxwb Mnrwo Dtgti Mcvpmduzzjap Perugia Italy
Jfekrt Bwuia Ziqqwotfqd Sqvxdmxno S-Hertogenbosch The Netherlands
Crdl Utzjwxgfud Huvxixfa Cork Ireland
Suc Opneo Hgtjgyqz Hy Trondheim Norway
Icagtuff Hziijfvyoqj I Txkyfcblxfdpfmt Warsaw Poland
Dmqztvhyggtrpccqx Snsotsqsx Dmclimusroykhyjzczmprd ubs Pzqwzquyigvuz gcfdy Stuttgart Germany
Maoewnsntspxygjrpyos Age Minden Germany
Grhth Hmmydaa Di Covvitvfr Charleroi Belgium
Gackuhwrar Ngfi gzsrk Khlbbjmxjtnqj Bmkzky Bremen Germany
Abdasn Stsfkzubhn Zmvqgxqzqc Dordrecht The Netherlands
Ujesddcqdsyohi Czdiblg Kgxdflupp Wqhynfaabaziq Ubzyrmoxsnqy Mstutebdkv Warsaw Poland
Hokbktan Ucixsaumzwsj Jtek Xcoxh Db Ttbjfgfdc Tarragona Spain
Mohbba Mgneepf Crlhpdo Veldhoven The Netherlands
Aqpvrle Slghfnnhr Lfvpzo Di Pxrlkhh Pescara Italy
Zgrljrzkmu Gxkx Geel Belgium
Kuenrcqo Pbcbvd Sbtagbv Gwfj Passau Germany
Sprtkxfcxsu Pfefjrskh Sonwykx Khrcbcxgw ilc Ac Moiyefjnfam Śta w Khphwrleog Katowice Poland

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

Trial status

Country Status Recruitment Start
Austria Austria
Not yet recruiting
15.12.2025
Belgium Belgium
Recruiting
15.12.2025
Denmark Denmark
Not yet recruiting
15.12.2025
Estonia Estonia
Recruiting
15.12.2025
Finland Finland
Recruiting
15.12.2025
Germany Germany
Recruiting
15.12.2025
Ireland Ireland
Not yet recruiting
15.12.2025
Italy Italy
Not yet recruiting
15.12.2025
Lithuania Lithuania
Not yet recruiting
15.12.2025
Norway Norway
Not yet recruiting
15.12.2025
Poland Poland
Not yet recruiting
15.12.2025
Spain Spain
Not yet recruiting
15.12.2025
Sweden Sweden
Recruiting
15.12.2025
The Netherlands The Netherlands
Recruiting
15.12.2025

Trial locations

Investigated Drugs:

Bleximenib is an investigational medication being studied in this trial. It is given in combination with standard chemotherapy during the initial treatment phase to help fight leukemia, and then continued as maintenance therapy. The purpose is to see if adding this medication to standard treatment can help prevent the cancer from coming back or getting worse in patients with certain types of acute myeloid leukemia.

Standard induction chemotherapy refers to the initial intensive treatment used to put the leukemia into remission. This means using powerful medications to kill as many cancer cells as possible and help the patient achieve a state where the disease is no longer detectable.

Consolidation chemotherapy is additional treatment given after the initial therapy to eliminate any remaining cancer cells and reduce the chance of the leukemia returning. This helps to strengthen and maintain the remission achieved with the induction treatment.

Investigated Diseases:

Acute Myeloid Leukemia – Acute Myeloid Leukemia is a type of cancer that affects the blood and bone marrow. It occurs when the bone marrow begins to produce abnormal white blood cells called myeloblasts, which do not function properly. These abnormal cells multiply rapidly and crowd out healthy blood cells in the bone marrow. As the disease progresses, the number of normal red blood cells, white blood cells, and platelets decreases. This leads to symptoms such as fatigue, frequent infections, easy bruising, and bleeding. The condition develops quickly and requires prompt medical attention.

Trial ID:
2025-522767-15-00
Protocol code:
HOVON 181 AML
Trial Phase:
Therapeutic confirmatory (Phase III)

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