Biomea Fusion Presents Preclinical Data Showing Icovamenib (BMF-219) Enhanced Effectiveness of GLP-1-Based Therapies and Introduces BMF-650, a Next-Generation, Oral Small-Molecule GLP-1 Receptor Agonist Candidate
Biomea Fusion presented preclinical data showing that icovamenib (BMF-219) enhanced the effectiveness of GLP-1-based therapies in diabetes treatment. Ex vivo human islet experiments demonstrated increased insulin secretion when icovamenib was combined with tirzepatide or semaglutide. The company plans to initiate a Phase II study (COVALENT-211) combining icovamenib with GLP-1-based therapy in 2025.
Additionally, Biomea introduced BMF-650, a next-generation oral small-molecule GLP-1 receptor agonist candidate, which showed promising preclinical results including improved glucose-stimulated insulin secretion, better glucose control, and appetite suppression in cynomolgus monkeys.
Biomea Fusion ha presentato dati preclinici che mostrano come icovamenib (BMF-219) aumenti l'efficacia delle terapie a base di GLP-1 nel trattamento del diabete. Esperimenti ex vivo su isole umane hanno dimostrato un aumento della secrezione di insulina quando l'icovamenib è stato combinato con tirzepatide o semaglutide. L'azienda prevede di avviare uno studio di Fase II (COVALENT-211) che combina icovamenib con terapia a base di GLP-1 nel 2025.
Inoltre, Biomea ha presentato BMF-650, un candidato agonista del recettore GLP-1 per via orale di nuova generazione, che ha mostrato risultati preclinici promettenti, tra cui un miglioramento nella secrezione di insulina stimolata dal glucosio, un migliore controllo della glicemia e soppressione dell'appetito nei macachi cynomolgus.
Biomea Fusion presentó datos preclínicos que muestran cómo icovamenib (BMF-219) mejora la efectividad de las terapias basadas en GLP-1 en el tratamiento de la diabetes. Experimentos ex vivo con islotes humanos demostraron un aumento en la secreción de insulina cuando icovamenib se combinó con tirzepatida o semaglutida. La empresa planea iniciar un estudio de Fase II (COVALENT-211) que combina icovamenib con terapia basada en GLP-1 en 2025.
Además, Biomea presentó BMF-650, un candidato agonista de receptor GLP-1 de nueva generación en forma de molécula pequeña y oral, que mostró resultados preclínicos prometedores, incluyendo una mejor secreción de insulina estimulado por glucosa, un mejor control de glucosa y supresión del apetito en monos cynomolgus.
Biomea Fusion은 icovamenib (BMF-219)가 당뇨병 치료에서 GLP-1 기반 요법의 효과를 향상시킨다는 전임상 데이터를 발표했습니다. Ex vivo 인간 췌장 섬 실험은 icovamenib이 tirzepatide 또는 semaglutide와 결합될 때 인슐린 분비가 증가함을 보여주었습니다. 회사는 2025년에 GLP-1 기반 요법과 icovamenib을 결합한 2상 연구 (COVALENT-211)를 시작할 계획입니다.
또한 Biomea는 경구용 소분자 GLP-1 수용체 작용제 후보인 BMF-650를 소개했으며, 이는 비임상 결과에서 포도당 자극 인슐린 분비 개선, 더 나은 포도당 조절 및 시노몰구스 원숭이에서 식욕 억제를 포함한 유망한 결과를 보였습니다.
Biomea Fusion a présenté des données précliniques montrant que icovamenib (BMF-219) améliore l'efficacité des thérapies basées sur le GLP-1 dans le traitement du diabète. Des expériences ex vivo sur des îlots humains ont démontré une augmentation de la sécrétion d'insuline lorsque l'icovamenib était combiné avec la tirzepatide ou la sémaglutide. L'entreprise prévoit de lancer une étude de Phase II (COVALENT-211) combinant icovamenib avec une thérapie basée sur le GLP-1 en 2025.
De plus, Biomea a présenté BMF-650, un candidat agoniste du récepteur GLP-1 de nouvelle génération sous forme de petite molécule orale, qui a montré des résultats précliniques prometteurs, y compris une amélioration de la sécrétion d'insuline stimulée par le glucose, un meilleur contrôle de la glycémie et une suppression de l'appétit chez les singes cynomolgus.
Biomea Fusion hat präklinische Daten vorgestellt, die zeigen, dass icovamenib (BMF-219) die Wirksamkeit von GLP-1-basierten Therapien zur Behandlung von Diabetes verbessert. Ex vivo Experimente mit menschlichen Inselzellen zeigten eine erhöhte Insulinsekretion, wenn icovamenib mit Tirzepatid oder Semaglutid kombiniert wurde. Das Unternehmen plant, 2025 eine Phase-II-Studie (COVALENT-211) zu starten, die icovamenib mit einer GLP-1-basierten Therapie kombiniert.
Zusätzlich stellte Biomea BMF-650 vor, einen Kandidaten für einen neuartigen oralen kleinen Molekül-GLP-1-Rezeptoragonisten, der vielversprechende präklinische Ergebnisse zeigte, einschließlich verbesserter glucosestimulierten Insulinsekretion, besserer Glukosekontrolle und Appetitzügelung bei Zynomolgusaffen.
- Preclinical data showed enhanced insulin secretion when combining icovamenib with GLP-1 therapies
- BMF-650 demonstrated higher bioavailability and less variable pharmacokinetic profile
- BMF-650 showed significant appetite suppression effects in preclinical studies
- Phase II combination study planned for 2025
- Both main drug candidates are still in early development stages
- Clinical efficacy in humans yet to be demonstrated for BMF-650
Insights
The preclinical data for icovamenib (BMF-219) and BMF-650 represents a significant development in diabetes treatment. The key findings show that icovamenib enhanced GLP-1 therapy effectiveness, with insulin secretion more than doubling under hyperglycemic conditions. BMF-650's preclinical results demonstrate superior bioavailability and consistent pharmacokinetics compared to existing oral GLP-1 RAs.
The planned Phase II COVALENT-211 study combining icovamenib with GLP-1 therapy could potentially address major challenges in current diabetes treatment, including efficacy and adherence. BMF-650's estimated 100mg once-daily dosing and demonstrated appetite suppression in primate studies suggest a promising profile for both diabetes and obesity indications. These developments could significantly impact the
This development positions Biomea Fusion strategically in the rapidly growing GLP-1 market. The dual approach of enhancing existing GLP-1 therapies with icovamenib while developing BMF-650 as a next-generation oral GLP-1 RA creates multiple potential revenue streams. The oral administration advantage could capture significant market share from injectable GLP-1 RAs like Ozempic and Wegovy, which face supply constraints and adherence challenges.
The combination therapy strategy could accelerate market penetration by leveraging existing GLP-1 prescriber networks. With obesity treatment market projections exceeding
- Preclinical data from ex vivo human islet experiments showed that icovamenib (BMF-219) was able to enhance the activity of glucagon-like peptide-1 (GLP-1)-based therapies, potentially leading to increased insulin secretion and improved glycemic control in patients with diabetes
- Phase II study (COVALENT-211), combining icovamenib with a GLP-1-based therapy, planned to begin in 2025
- BMF-650, an investigational next-generation, oral small-molecule GLP-1 receptor agonist (GLP-1 RA), demonstrated positive early preclinical activity, including improved glucose-stimulated insulin secretion, reduction in blood glucose concentration, and appetite suppression in cynomolgus monkeys
REDWOOD CITY, Calif., Oct. 30, 2024 (GLOBE NEWSWIRE) -- Biomea Fusion, Inc. (“Biomea” or “the Company”) (Nasdaq: BMEA), a clinical-stage biopharmaceutical company dedicated to discovering and developing oral covalent small molecules to improve the lives of patients with diabetes, obesity, and genetically defined cancers, today presented preclinical data showing icovamenib enhanced the activity of GLP-1-based therapies, along with early preclinical efficacy and pharmacokinetic data for BMF-650, a next-generation, oral small-molecule GLP-1 RA candidate.
“Menin plays a central role in the pancreas, not only impacting the proliferation of beta cells but also the expression of GLP-1 receptors. We observed that icovamenib, when combined with either of the two most commonly used GLP-1-based therapies, tirzepatide or semaglutide, enhanced the responsiveness of human islets to the GLP-1-based therapy, leading to substantial insulin secretion under hyperglycemic conditions. The dose-dependent improvements, where glucose-stimulated insulin secretion more than doubled, are highly promising,” stated Juan Pablo Frias, MD, Biomea Fusion’s Chief Medical Officer. “Additionally, we believe the results we’ve seen with our own GLP-1 RA product candidate, BMF-650, highlight a strong potential as a next-generation, oral GLP-1 RA for both diabetes and obesity. We believe these findings open exciting new avenues for treatment.”
Icovamenib (BMF-219) in Combination with a GLP-1-Based Therapy
Key Highlights:
- Preclinical studies evaluated insulin secretion by GLP-1-based therapies (tirzepatide and semaglutide) using human islets cultured ex vivo under hyperglycemic conditions, with and without icovamenib treatment.
- We hypothesized that menin inhibition would enhance the effectiveness of GLP-1-based therapies and showcased functional data, indicating stronger insulin responses with both tirzepatide and semaglutide when combined with icovamenib treatment.
- Further studies with orforglipron also indicated that icovamenib pretreatment improved insulin secretion, approximately doubling the effect-size depending on the dose.
- Additionally, BMF-650, Biomea’s next-generation, oral small molecule GLP-1 RA product candidate, used alone or in combination with icovamenib, yielded even further improved results supporting the potential for therapeutic benefits.
- The initiation of a Phase II study, COVALENT-211, to evaluate the combination of icovamenib with a GLP-1-based therapy, is planned for 2025.
In addition, the Company announced additional details about its investigational, next-generation, oral small-molecule GLP-1 RA candidate, BMF-650.
BMF-650 - an Investigational, Next-Generation, Oral Small Molecule GLP-1 Receptor Agonist - Key Highlights:
- We conducted preclinical studies to evaluate the properties of BMF-650 in comparison to a leading oral GLP-1 RA. BMF-650 exhibited higher bioavailability and a less variable pharmacokinetic profile, which may translate to improved tolerability and support successful dose escalation in patients. The estimated human dose will be approximately 100 mg once daily.
- In human donor islet studies, BMF-650 significantly enhanced glucose-stimulated insulin secretion.
- In cynomolgus monkey studies, BMF-650 showed significant improvements in glucose stimulated insulin secretion, in line with findings from the human donor islet experiments. BMF-650 also demonstrated superior glucose control.
- Appetite suppression studies revealed that daily oral BMF-650 dosing significantly reduced food intake during peak drug concentration, with sustained effects throughout the day for a six-day study period.
- These findings highlight BMF-650’s potential as an oral treatment for diabetes and obesity.
“Our preclinical findings about the inhibition of menin in the GLP-1 pathway, announced today, may support the profile of icovamenib as a potential combination agent for GLP-1-based therapies. With the combination of icovamenib, less GLP-1 RA dosing may be required, which may support the overall benefits of these therapeutics. We believe, icovamenib may contribute to improved efficacy, tolerability and adherence, which ultimately will lead to more patients having longer benefits from these agents. We plan to clinically evaluate icovamenib as an adjunct to GLP-1-based therapies,” stated Thomas Butler, Biomea Fusion’s Chief Executive Officer and Chairman of the Board. “We are equally excited with the early results of our newest asset, BMF-650, which demonstrated clear advantages, including when compared to a leading GLP-1 RA in our preclinical studies. BMF-650 has shown superior insulin secretion, better glucose control, a smoother pharmacokinetic profile and higher bioavailability; all of which point to the potential for a greater therapeutic window and support our plans to evaluate BMF-650 as a next-generation oral treatment for diabetes. The appetite suppression results were particularly exciting, as they signal a new and impactful profile which we believe may support an impact on obesity.”
Conference Call and Webcast Details
Webcast, and related presentation, of Biomea’s investor update on Wednesday, October 30 at 4:30 pm ET will be available to registered attendees under the Investors and Media section of the company’s website at https://investors.biomeafusion.com/news-events/events. A replay of the presentation will be available on Biomea’s site following the event.
About Obesity
Obesity is a chronic disease necessitating long-term management, associated with diminished life expectancy and a spectrum of severe health complications. These include metabolic disorders such as type 2 diabetes and non-alcoholic fatty liver disease; cardiovascular diseases like heart attack, stroke, and hypertension; and increased risks of chronic kidney disease, certain cancers, and chronic inflammation. The CDC estimates that over
About GLP-1 Receptor Agonists
Glucagon-like peptide-1 (GLP-1) is a naturally occurring incretin hormone that plays a vital role in glucose homeostasis and appetite regulation. GLP-1 receptor agonists (GLP-1 RAs) are a class of medications that bind to and activate GLP-1 receptors, mimicking the effects of native GLP-1. These agents have demonstrated robust clinical efficacy in improving glycemic control, promoting weight loss, and enhancing insulin sensitivity in individuals with type 2 diabetes and obesity.
About Biomea Fusion
Biomea Fusion is a clinical-stage biopharmaceutical company focused on the discovery and development of oral covalent small molecules to improve the lives of patients with diabetes, obesity, and genetically defined cancers. A covalent small molecule is a synthetic compound that forms a permanent bond to its target protein and offers a number of potential advantages over conventional non-covalent drugs, including greater target selectivity, lower drug exposure, and the ability to drive a deeper, more durable response.
We are utilizing our proprietary FUSION™ System to discover, design and develop a pipeline of next-generation covalent-binding small-molecule medicines designed to maximize clinical benefit for patients. We aim to have an outsized impact on the treatment of disease for the patients we serve. We aim to cure.
Visit us at biomeafusion.com and follow us on LinkedIn, X and Facebook.
Forward-Looking Statements
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Contact:
Investor & Media Relations
Ramses Erdtmann
re@biomeafusion.com
FAQ
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