Dianthus Therapeutics Announces Two Poster Presentations for DNTH103 at the 2024 American Association of Neuromuscular and Electrodiagnostic Medicine (AANEM) Annual Meeting
Dianthus Therapeutics (Nasdaq: DNTH) announced two poster presentations for DNTH103 at the 2024 American Association of Neuromuscular and Electrodiagnostic Medicine (AANEM) Annual Meeting in Savannah, Georgia. DNTH103 is an investigational classical pathway inhibitor specific to the active form of C1s, being evaluated for generalized Myasthenia Gravis, Multifocal Motor Neuropathy, and Chronic Inflammatory Demyelinating Polyneuropathy.
The presentations will showcase:
- Preclinical and in vitro data on DNTH103's potentially differentiated profile in disease models of gMG and CIDP
- Head-to-head affinity and pharmacodynamic potency data comparing DNTH103 to riliprubart
- DNTH103's sustainable inhibition of complement and prevention of nerve conduction velocity impairment in a CIDP preclinical model
- DNTH103 as a potentially safer and more convenient novel therapy for generalized Myasthenia Gravis
The posters will be available on the Dianthus website after presentation.
Dianthus Therapeutics (Nasdaq: DNTH) ha annunciato due presentazioni di poster per DNTH103 durante il 2024 American Association of Neuromuscular and Electrodiagnostic Medicine (AANEM) Annual Meeting a Savannah, Georgia. DNTH103 è un inibitore della via classica specifico per la forma attiva del C1s, attualmente in fase di valutazione per la Miastenia Gravis generalizzata, la Neuropatia motoria multifocale e la Polineuropatia infiammatoria demielinizzante cronica.
Le presentazioni mostreranno:
- Dati preclinici e in vitro sul potenziale profilo differenziato di DNTH103 in modelli di gMG e CIDP
- Dati di affinità e potenza farmacodinamica a confronto tra DNTH103 e riliprubart
- Inibizione sostenibile del complemento e prevenzione del deterioramento della velocità di conduzione nervosa in un modello preclinico di CIDP con DNTH103
- DNTH103 come terapia potenzialmente più sicura e conveniente per la miastenia gravis generalizzata
I poster saranno disponibili sul sito web di Dianthus dopo la presentazione.
Dianthus Therapeutics (Nasdaq: DNTH) anunció dos presentaciones de póster para DNTH103 en la Reunión Anual de la Asociación Americana de Medicina Neuromuscular y Electrodiagnóstica (AANEM) 2024 en Savannah, Georgia. DNTH103 es un inhibidor investigacional de la vía clásica específico para la forma activa de C1s, que se está evaluando para la Miastenia Gravis generalizada, la Neuropatía Motoras Multifocal y la Polineuropatía Crónica Inflamatoria Desmielinizante.
Las presentaciones mostrarán:
- Datos preclínicos e in vitro sobre el perfil potencialmente diferenciado de DNTH103 en modelos de gMG y CIDP
- Datos de afinidad y potencia farmacodinámica en comparación entre DNTH103 y riliprubart
- Inhibición sostenible del complemento y prevención del deterioro de la velocidad de conducción nerviosa en un modelo preclínico de CIDP con DNTH103
- DNTH103 como una terapia novel potencialmente más segura y conveniente para la miastenia gravis generalizada
Los pósteres estarán disponibles en el sitio web de Dianthus después de la presentación.
디안투스 테라퓨틱스 (Nasdaq: DNTH)는 조지아주 사바나에서 열리는 2024 미국 신경근육 및 전기진단 의학회(AANEM) 연례 회의에서 DNTH103에 대한 두 가지 포스터 발표를 발표했습니다. DNTH103은 C1s의 활성 형태에 특정한 고전적 경로 억제제로, 전신형 미astenia gravis, 다초점 운동 신경병증 및 만성 염증 탈수초성 다발신경병증에 대한 평가가 진행되고 있습니다.
발표 내용은 다음과 같습니다:
- gMG와 CIDP 질병 모델에서 DNTH103의 잠재적으로 차별화된 프로필에 대한 전임상 및 인비트로 데이터
- DNTH103과 릴리푸르바르트 간의 직접 비교를 통한 친화도 및 약리학적 효능 데이터
- CIDP 전임상 모델에서 DNTH103의 보완 지속적 억제 및 신경 전도 속도 손상 예방
- DNTH103이 전신형 미astenia gravis에 대한 잠재적으로 더 안전하고 편리한 새로운 치료법으로서의 가능성
포스터는 발표 후 디안투스 웹사이트에서 확인할 수 있습니다.
Dianthus Therapeutics (Nasdaq: DNTH) a annoncé deux présentations de posters pour DNTH103 lors de la Réunion Annuelle de l'Association Américaine de Médecine Neuromusculaire et d'Électrodiagnostic (AANEM) 2024 à Savannah, en Géorgie. DNTH103 est un inhibiteur de la voie classique en cours d'investigation, spécifique à la forme active de C1s, et est évalué pour la Myasthénie Gravis généralisée, la Neuropathie Motrice Multifocale et la Polynévropathie Inflammatoire Démyélinisante Chronique.
Les présentations mettront en avant :
- Données précliniques et in vitro sur le profil potentiellement différencié de DNTH103 dans des modèles de gMG et de CIDP
- Données d'affinité et de puissance pharmacodynamique comparant DNTH103 à riliprubart
- Inhibition durable du complément et prévention de l'altération de la vitesse de conduction nerveuse dans un modèle préclinique de CIDP avec DNTH103
- DNTH103 comme une thérapie nouvelle potentiellement plus sûre et plus pratique pour la Myasthénie Gravis généralisée
Les posters seront disponibles sur le site Web de Dianthus après la présentation.
Dianthus Therapeutics (Nasdaq: DNTH) gab zwei Posterpräsentationen für DNTH103 auf dem 2024 American Association of Neuromuscular and Electrodiagnostic Medicine (AANEM) Annual Meeting in Savannah, Georgia bekannt. DNTH103 ist ein experimenteller Inhibitor des klassischen Weges, der spezifisch für die aktive Form von C1s ist und derzeit für generalisierte Myasthenia gravis, multifokale motorische Neuropathie und chronische entzündliche demyelinisierende Polyneuropathie bewertet wird.
Die Präsentationen werden Folgendes zeigen:
- Präklinische und in vitro Daten zu DNTH103s potenziell differenziertem Profil in Krankheitsmodellen von gMG und CIDP
- Vergleichsdaten zu Affinität und pharmakodynamischer Potenz zwischen DNTH103 und Riliprubart
- Die nachhaltige Hemmung des Komplements und die Verhinderung einer Beeinträchtigung der Nervenleitgeschwindigkeit bei einem präklinischen CIDP-Modell mit DNTH103
- DNTH103 als potenziell sicherere und bequemere Neu-Therapie für generalisierte Myasthenia gravis
Die Poster werden nach der Präsentation auf der Webseite von Dianthus verfügbar sein.
- Presentation of preclinical and in vitro data for DNTH103 at a major medical conference
- Potential differentiated profile of DNTH103 in gMG and CIDP disease models
- Head-to-head comparison data with riliprubart, showcasing DNTH103's affinity and pharmacodynamic potency
- None.
NEW YORK and WALTHAM, Mass., Oct. 15, 2024 (GLOBE NEWSWIRE) -- Dianthus Therapeutics, Inc. (Nasdaq: DNTH), a clinical-stage biotechnology company dedicated to advancing the next generation of antibody complement therapeutics to treat severe autoimmune diseases, today announced two poster presentations for DNTH103 at the 2024 American Association of Neuromuscular and Electrodiagnostic Medicine (AANEM) Annual Meeting, taking place October 15-18, 2024 in Savannah, Georgia.
DNTH103 is an investigational classical pathway inhibitor that is uniquely specific to the active form of C1s, and is being evaluated for its potential as an effective, low-volume, convenient and safe treatment option for patients with generalized Myasthenia Gravis, Multifocal Motor Neuropathy, and Chronic Inflammatory Demyelinating Polyneuropathy.
Two poster presentations at AANEM will highlight preclinical and in vitro data describing the potentially differentiated profile of DNTH103 in disease models of generalized Myasthenia Gravis (gMG) and Chronic Demyelinating Polyneuropathy (CIDP), in addition to head-to-head affinity and pharmacodynamic (PD) potency data for DNTH103 compared to riliprubart.
Dianthus Presentations at AANEM:
October 16, 2024, 6:15-6:45 PM ET & October 17, 2024, 2:45-3:15 PM ET
DNTH103 Shows Sustainable Inhibition of Complement and Prevents Nerve Conduction Velocity Impairment in a Preclinical Model of CIDP
Poster #201
October 16, 2024, 6:15-6:45 PM ET & October 17, 2024, 9:30-10:00 AM ET
DNTH103, A Potentially Safer and More Convenient Novel, Investigational Therapy for Generalized Myasthenia Gravis
Poster #297
These posters will be made available in the Scientific Publications section of the Dianthus website after they are presented.
About DNTH103
DNTH103 is an investigational, clinical-stage, potent monoclonal antibody engineered to selectively target the classical pathway by inhibiting only the active form of the C1s protein, a clinically validated complement target. DNTH103 is enhanced with YTE half-life extension technology designed to enable a more convenient subcutaneous, self-administered injection dosed as infrequently as once every two weeks. Additionally, selective inhibition of the classical complement pathway may lower patient risk of infection from encapsulated bacteria by preserving immune activity of the lectin and alternative pathways. As the classical pathway plays a significant role in disease pathology, DNTH103 has the potential to be a best-in-class pipeline-in-a-product across a range of autoimmune disorders with high unmet need. Dianthus is building a neuromuscular franchise with DNTH103 following the initiation of the Phase 2 MaGic trial in generalized Myasthenia Gravis in 1Q’24 and the Phase 2 MoMeNtum trial in Multifocal Motor Neuropathy in 3Q’24, and planned initiation of a Phase 2 trial in Chronic Inflammatory Demyelinating Polyneuropathy in 2H’24.
DNTH103 is an investigational agent that is not approved as a therapy in any indication in any jurisdiction worldwide.
About Dianthus Therapeutics
Dianthus Therapeutics is a clinical-stage biotechnology company dedicated to designing and delivering novel, best-in-class monoclonal antibodies with improved selectivity and potency. Based in New York City and Waltham, Mass., Dianthus is comprised of an experienced team of biotech and pharma executives who are leading the development of next-generation antibody complement therapeutics, aiming to deliver transformative medicines for people living with severe autoimmune and inflammatory diseases.
To learn more, please visit www.dianthustx.com and follow us on LinkedIn.
Cautionary Statement Regarding Forward-Looking Statements
Certain statements in this press release, other than purely historical information, may constitute “forward-looking statements” within the meaning of the federal securities laws, including for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995, express or implied statements regarding future plans and prospects, including statements regarding the expectations or plans for discovery, preclinical studies, clinical trials and research and development programs, in particular with respect to DNTH103, and any developments or results in connection therewith, including the target product profile of DNTH103; the anticipated timing of the initiation and results from those studies and trials; expectations regarding the time period over which the Company’s capital resources are expected to be sufficient to fund its anticipated operations; and expectations regarding the market and potential opportunities for complement therapies, in particular with respect to DNTH103. The words “opportunity,” “potential,” “milestones,” “runway,” “will,” “anticipate,” “achieve,” “near-term,” “catalysts,” “pursue,” “pipeline,” “believe,” continue,” “could,” “estimate,” “expect,” “ intend,” “may,” “might,” “plan,” “possible,” “predict,” “project,” “ should,” “strive,” “would,” “aim,” “target,” “commit,” and similar expressions (including the negatives of these terms or variations of them) generally identify forward-looking statements, but the absence of these words does not mean that statement is not forward looking.
Actual results could differ materially from those included in the forward-looking statements due to various factors, risks and uncertainties, including, but not limited to, that preclinical testing of DNTH103 and data from clinical trials may not be predictive of the results or success of ongoing or later clinical trials, that the development of DNTH103 or the Company's other compounds may take longer and/or cost more than planned, that the Company may be unable to successfully complete the clinical development of the Company’s compounds, that the Company may be delayed in initiating, enrolling or completing its planned clinical trials, and that the Company's compounds may not receive regulatory approval or become commercially successful products. These and other risks and uncertainties are identified under the heading "Risk Factors" included in the Company’s Annual Report on Form 10-K for the period ended December 31, 2023, and other filings that the Company has made and may make with the SEC in the future. Nothing in this press release should be regarded as a representation by any person that the forward-looking statements set forth herein will be achieved or that any of the contemplated results of such forward-looking statements will be achieved.
The forward-looking statements in this press release speak only as of the date they are made and are qualified in their entirety by reference to the cautionary statements herein. Dianthus undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events or otherwise, except as required by law.
Contact
Jennifer Davis Ruff
Dianthus Therapeutics
jdavisruff@dianthustx.com
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