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212 Bleximenib Dose Optimization and Determination of RP2D from a Phase 1 Study in Relapsed/Refractory Acute Leukemia Patients with KMT2A and NPM1 Alterations

Program: Oral and Poster Abstracts
Type: Oral
Session: 616. Acute Myeloid Leukemias: Investigational Drug and Cellular Therapies: Menin Inhibitors in AML
Hematology Disease Topics & Pathways:
Clinical trials, Research, Lymphoid Leukemias, ALL, Acute Myeloid Malignancies, AML, Adult, Drug development, Clinical Research, Diseases, Treatment Considerations, Biological therapies, Lymphoid Malignancies, Myeloid Malignancies, Study Population, Human
Saturday, December 7, 2024: 2:15 PM

Emma Searle, MD, PhD1*, Christian Recher, MD, PhD2*, Maher Abdul-Hay, MD3*, Sameem Abedin, MD4, Ibrahim Aldoss, MD5, Ana Alfonso Pierola, MD, PhD6*, Juan M. Alonso-Dominguez, MD, PhD7*, Patrice Chevallier, MD, PhD8, Carrye Cost, MD9*, Nikki Daskalakis, MD9*, Richard Dillon, MA10, Neil Dunavin, MD, MS11*, Jordi Esteve, MD, PhD12, Amir T. Fathi, MD13, Pasquale L. Fedele, MBBS, PhD, FRACP, FRCPA14*, Lucille Ferrante, MD, MS9, Stan Gaj, MSc15*, Christina Guttke, PhD9*, Emmanuel Gyan, MD, PhD16, Brett Hiebert, MS17*, Elias Jabbour, MD18, Hagop M. Kantarjian, MD18, Min Chul Kwon, PhD15, Anita J Kumar, MD, MSCE, PhD9, Teng Fong Ng, BSc, MBBS, MRCP, FRACP, FRCPA19*, Kathryn Packman, PhD20*, Ulrike Philippar, PhD21, Arnaud Pigneux, MD, PhD22*, Olga Salamero, MD23*, Madhu Sanga, PhD24*, Prathap Nagaraja Shastri, PhD9*, Richard M. Stone, MD25, Peter T. Tan, MBBS26, Trevor Tucker, BS9*, Paresh Vyas, FMedSci, DPhil, FRCPath27* and Sylvain Garciaz, MD28*

1The Christie NHS Foundation Trust and University of Manchester, Manchester, United Kingdom
2University Cancer Institute Toulouse Oncopole, Toulouse, France
3Blood and Marrow Transplantation and Cellular Therapy, Laura and Issac Perlmutter Cancer Center at NYU Langone Health, New York, NY
4Medical College of Wisconsin, Milwaukee, WI
5City of Hope National Medical Center, Duarte, CA
6Clínica Universidad de Navarra, Navarra, Spain
7Hospital Universitario Fundacion Jimenez Diaz - IISFJD-UAM, Madrid, Spain
8Nantes University Hospital, Nantes, France
9Janssen Research & Development, LLC, Spring House, PA
10Guy's and St Thomas' NHS Foundation Trust and King's College London, London, United Kingdom
11University of California San Francisco, San Francisco, CA
12Hematology Department, Hospital Clínic de Barcelona, Barcelona, Spain
13Massachusetts General Hospital, Harvard Medical School, Boston, MA
14Monash Health and School of Clinical Sciences at Monash Health, Monash University, Clayton, VIC, Australia
15Janssen Research & Development, LLC, Beerse, Belgium
16Centre Hospitalier Universitaire de Tours, Tours, France
17IQVIA, Winnipeg, MB, Canada
18MD Anderson Cancer Center, University of Texas, Houston, TX
19Gold Coast University Hospital and Griffith University, Queensland, Australia
20Janssen Research & Development, LLC, Cambridge, MA
21Janssen Research & Development, Beerse, Belgium
22Hopital Haut Leveque, Pessac, France
23University Hospital Vall d’Hebron, and Experimental Hematology, Vall d’Hebron Institute of Oncology, Barcelona, Spain
24Janssen Research & Development, LLC, Brisbane, CA
25Dana-Farber Cancer Institute, Boston, MA
26Royal Perth Hospital, Perth, Australia
27Radcliffe Department of Medicine, Weatherall Institute of Molecular Medicine, Oxford, United Kingdom
28Aix-Marseille Université, Inserm, CNRS, Institut Paoli-Calmettes, Centre de Recherche en Cancérologie de Marseille, Marseille, France

Background: Despite improvements in treatment for acute leukemia (AL), outcomes for patients with relapsed/refractory (R/R) disease remain poor. Novel therapies are needed to treat AL with KMT2A (9–15% of adult acute myeloid leukemia [AML], 10% of acute lymphoblastic leukemia [ALL]) and NPM1 (30% of adult AML) alterations. Bleximenib (JNJ-75276617) is a potent, selective inhibitor of the menin-KMT2A interaction and is being evaluated as monotherapy in R/R AL with KMT2A or NPM1 alterations (NCT04811560). Here we report data that informed the recommended phase 2 dose (RP2D) from the ongoing Phase 1 multicenter dose-finding study of bleximenib monotherapy for KMT2A- or NPM1- altered R/R AL. The aim of this study is to determine the RP2D of bleximenib and establish the safety and tolerability at the RP2D. This study also explores the pharmacokinetics (PK), pharmacodynamics (PD), and preliminary clinical activity of bleximenib at the RP2D.

Methods: Participants (pts) in dose-escalation receive bleximenib orally on a 28-day cycle, with step-up dosing to mitigate the risk of differentiation syndrome (DS) and to optimize therapeutic exposures. Adverse events (AEs) are graded using the CTCAE v5.0. The safety dataset comprises pts who have received at least one dose of bleximenib. Efficacy responses are investigator-assessed per modified ELN 2017 in pts with R/R NPM1-mutated (NPM1m) or KMT2A-rearranged (KMT2Ar) AL.

Results: As of July 2024, 121 pts with R/R AL (AML, n=108; ALL, n=6; other AL, n=7) received study treatment (median age: 61 years [range: 18–85] years; 55% female; 82% White; 36% Eastern Cooperative Oncology Group Performance Status of 0). KMT2A and NPM1 alterations were present in 73 (60%) and 48 (40%) pts, respectively. Median number of prior lines of therapy was 2 (range: 1–7); 25% (30/121) had ≥1 prior allograft.

To determine the RP2D, data were evaluated using 3 composite treatment dose subgroups: 45 mg twice daily (BID; n=15), 90/100 mg BID (n=27), and 150 mg BID (n=28). Data from 90/100 mg BID (RP2D) pts were combined, given the similar doses and overlapping PK exposures.

Treatment-related AEs (TRAEs) of any grade (G) occurred in 70/121 (58%) pts, most commonly DS (13%), neutropenia (12%), thrombocytopenia (11%), and nausea (9%). Seventeen pts experienced DS (both KMT2A and NPM1), with 8 (7%) DS events ≥G3, including 2 fatal events. One fatal DS AE occurred in a pt with recurrent DS after rapid dose escalation. A single related AE of QTc prolongation (G3, dose-limiting toxicity [DLT]) was observed in a pt with significant cardiac comorbidities at once daily dosing without step-up. TRAEs ≥G3 were observed in 40/121 (33%) pts, most commonly neutropenia (11%), thrombocytopenia (8%), and DS (7%), with an increased incidence of ≥G3 TRAEs (11 pts [39%]) observed at 150 mg BID. G4 TRAEs of thrombocytopenia were more common at 150 mg BID (3 [11%]) versus 100 mg BID (2 [7%]) or 45 mg BID (0%), and more G4 neutropenia DLTs were reported at 150 mg BID. Bleximenib-related dose interruptions and reductions were more frequent at 150 mg BID (25% and 14%), compared to 90/100 mg BID (7% and 7%), or 45 mg BID (7% and 7%), respectively.

Overall response rate (ORR: ≥PR) was 50% (10/20) at both 90/100 mg BID and 150 mg BID, while the ORR observed at 45 mg BID was 39% (5/13). Composite complete response (cCR; CR/CRh/CRi) rates were identical at 90/100 mg BID and 150 mg BID (8/20 [40%] each) and lower at 45 mg BID (3/13 [23%]). The CR/CRh rate was higher at 90/100 mg BID (7/20 [35%]) and 150 mg BID (6/20 [30%]) versus 45 mg BID (3/13 [23%]). Median time to first response at 90/100 mg BID was 30 days (range: 27–85), and median duration of response was 6.4 months (95% CI: 0.1–NE). ORR and cCR were similar between KMT2Ar and NPM1m AML. Bleximenib exposures corresponding to 90/100 mg BID resulted in reduced hematologic toxicity, optimized PD effect with MEIS1 reduction, and maximal efficacy as evidenced by exposure safety and efficacy analyses.

Conclusion: When compared to other dose levels explored, the data informed a bleximenib RP2D of 100 mg BID (after a 50 mg BID step-up dose) with optimal safety, PK exposure, and PD response, and promising antileukemic activity as monotherapy in R/R AML harboring KMT2Ar or NPM1m. No cardiac safety signal was observed, and mitigation measures have been implemented for DS. Phase 2 clinical trial activation is ongoing to further evaluate bleximenib monotherapy at the RP2D in R/R AML with KMT2Ar or NPM1m.

Disclosures: Searle: Janssen, Abbvie, Beigene, BMS, Nurix: Honoraria; Pfizer, Janssen, Jazz, Abbvie: Speakers Bureau; Shattuck Labs, Sanofi, BMS, DarkBlue Therapeutics: Consultancy. Recher: Abbvie, Astellas, BMS, Daiichi-Sankyo, Iqvia and Jazz Pharmaceuticals: Other: Research Funding to my institution. Abdul-Hay: Amgen, Incyte, Novartis, Takeda, Daiichi, Kite: Other: Advisory board; Amgen: Membership on an entity's Board of Directors or advisory committees, Other: Advisory Board ; Incyte: Membership on an entity's Board of Directors or advisory committees, Other: Advisory Board; Novartis: Membership on an entity's Board of Directors or advisory committees, Other: Advisory Board; Takeda: Membership on an entity's Board of Directors or advisory committees, Other: Advisory Board ; Daiichi: Membership on an entity's Board of Directors or advisory committees, Other: Advisory Board; Kite: Membership on an entity's Board of Directors or advisory committees, Other: Advisory Board ; PureTech: Consultancy, Other: Consultant; Abbvie: Consultancy, Other: Consultant . Abedin: AbbVie, Daichii Sankyo, Servier: Consultancy, Honoraria; Actinium Pharmaceutical, AltruBio, Incyte: Research Funding. Aldoss: Kite Pharma: Other: consulting fees; Pfizer: Honoraria, Other: consulting fees; Takeda Pharmaceuticals: Other: consulting fees; Syndax Pharmaceuticals, Inc.: Other: consulting fees; Jazz Pharmaceuticals: Other: consulting fees; Sobi: Other: consulting fees; AbbVie: Other: research support; Amgen: Honoraria, Other: consulting fees. Pierola: Abbvie, BMS, Jazz Pharma, Novartis, Syros: Speakers Bureau; Astellas, BMS, Jazz Pharma, Syros: Consultancy; AstraZeneca: Research Funding. Alonso-Dominguez: Astellas: Research Funding; Astellas, Servier: Other: Advisory Board. Cost: Johnson & Johnson: Current Employment. Daskalakis: Janssen: Current Employment, Current equity holder in private company; Sanofi: Current equity holder in private company. Dillon: Abbvie, Amgen: Other: Research support (paid to institution); Jazz: Other: Consultancy and educational events (paid to institution); Abbvie, Astellas, Pfizer: Consultancy, Other: Educational events. Fathi: EnClear: Consultancy; Servier: Consultancy, Research Funding; Astellas: Consultancy; Agios: Ended employment in the past 24 months; BMS/Celgene: Consultancy; ImmunoGen: Consultancy; Ipsen: Consultancy; Mablytics: Consultancy; Novartis: Consultancy; Bristol Myers Squibb: Consultancy, Research Funding; AstraZeneca: Honoraria; Remix: Consultancy; Menarini Group: Consultancy; Orum: Consultancy; Foghorn, Blueprint Medicines, Kura, Trillium: Honoraria; MorphoSys: Consultancy; Kite: Consultancy; AbbVie, BMS/Celgene, and Agios/Servier: Research Funding; Genentech: Honoraria; Gilead: Consultancy; Ispen: Consultancy; Abbvie: Consultancy, Research Funding; PureTech: Consultancy; Takeda: Consultancy; Amgen: Consultancy; Forma: Consultancy; Daiichi Sankyo: Consultancy; Pfizer: Consultancy; Rigel: Consultancy; Autolus: Consultancy. Fedele: Amgen, Pfizer, Adaptive Biosciences: Membership on an entity's Board of Directors or advisory committees; BMS: Research Funding. Ferrante: Johnson & Johnson: Current Employment. Gaj: Janssen R&D (Johnson & Johnson): Current Employment. Guttke: Johnson & Johnson Innovative Medicine: Current Employment, Current holder of stock options in a privately-held company, Patents & Royalties. Gyan: BMS, Sandoz: Research Funding; AstraZeneca, Abbvie, Janssen, Roche, BMS, Sanofi, Kephren Publishing, Recordati, Novartis, Incyte, Axonal, Servier, Gilead Kite: Honoraria. Hiebert: Johnson & Johnson: Other: Functional Service Provider (FSP) from IQVIA . Jabbour: AbbVie, Adaptive Biotechnologies, Amgen, Astellas Pharma, BMS, Genentech, Incyte, Pfizer, Takeda: Consultancy; AbbVie, Adaptive Biotechnologies, Amgen, Ascentage Pharma Group, Pfizer, Takeda: Research Funding. Kantarjian: AbbVie, Amgen, Ascentage, Ipsen Biopharmaceuticals, KAHR Medical, Novartis, Pfizer, Shenzhen Target Rx, Stemline,Takeda: Consultancy, Honoraria. Kwon: Janssen: Current Employment. Kumar: Johnson & Johnson: Current Employment; Flatiron Health: Ended employment in the past 24 months. Ng: Spinnaker Health Research foundation: Research Funding; WA Health: Other: Fellowship Grant; University hospital Geelong: Other: Project Grant. Packman: Janssen: Current Employment, Current equity holder in publicly-traded company. Philippar: Johnson&Johnson Innovative Medicine: Current Employment, Current holder of stock options in a privately-held company, Membership on an entity's Board of Directors or advisory committees, Patents & Royalties. Salamero: Astellas, Jazz, BMS: Consultancy; Jazz, Abbvie: Honoraria. Sanga: Alcon Laboratories, inc: Current equity holder in publicly-traded company; Janssen: Current Employment, Current equity holder in publicly-traded company, Divested equity in a private or publicly-traded company in the past 24 months. Nagaraja Shastri: Johnson & Johnson: Current Employment, Current equity holder in publicly-traded company. Stone: AvenCell: Consultancy; Syntrix: Other: DSMB; Jazz: Consultancy; Hermavant: Consultancy; Glaxosmithkline: Consultancy; Glycomimetrics: Consultancy; AMGEN: Consultancy; Rigel: Consultancy; Daiichi Sankyo: Consultancy; Janssen: Other: Research funding to my institution; Redona therapeutics: Consultancy; Epizyme: Consultancy, Other: DSMB; ENSEM: Consultancy; Novartis: Other: Research funding to my institution; Ligand Pharma: Consultancy; Lava Therapeutics: Consultancy; Kura Oncology: Consultancy; Aptevo: Consultancy; CTI Biopharma: Consultancy; Curis Oncology: Consultancy; Syndax: Other: Research funding to my institution; Cellarity: Consultancy; BerGenBio: Consultancy; Bristol Meyers Squibb: Consultancy; AbbVie: Consultancy, Other: Research funding to my institution; Takeda: Other: DSMB. Tucker: Johnson & Johnson: Current Employment, Current equity holder in publicly-traded company; Kura Oncology: Current equity holder in publicly-traded company; Guardant Health: Current equity holder in publicly-traded company; Viridian Therapeutics: Current equity holder in publicly-traded company; Cullinan Oncology: Current equity holder in publicly-traded company; Voyager Therapeutics: Current equity holder in publicly-traded company; Tracon Pharmaceuticals: Current equity holder in publicly-traded company; Erasca INC: Current equity holder in publicly-traded company; Bellicum Pharmaceuticals: Current equity holder in publicly-traded company; G1 Therapeutics: Current equity holder in publicly-traded company. Vyas: Abbvie, Servier, Rigel, Syndax, AstraZeneca, Debiopharm, Charm Therapeutics: Consultancy; Yellowstone Biosciences: Current equity holder in private company, Current holder of stock options in a privately-held company, Membership on an entity's Board of Directors or advisory committees, Research Funding; BMS: Research Funding; Auron Therapeutics: Membership on an entity's Board of Directors or advisory committees. Garciaz: Janssen: Consultancy, Honoraria; Imcheck Therapeutics: Consultancy; Servier: Consultancy, Honoraria; Sanofi: Consultancy, Other: travel grant; Abbvie: Consultancy, Honoraria, Other: Travel grant; BMS: Consultancy.

*signifies non-member of ASH