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Altimmune to Present New Data on the Lipidomic Profile in Subjects Treated with Pemvidutide at The Liver Meeting® 2024

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Altimmune (Nasdaq: ALT) announced new data on the lipidomic profile of subjects treated with pemvidutide will be presented at The Liver Meeting® 2024 of the American Association for the Study of Liver Diseases (AASLD) in San Diego, CA, November 15-19, 2024. The data shows reductions in multiple classes of atherogenic and cardio-inflammatory lipids from a 12-week Phase 1b randomized, placebo-controlled study in subjects with metabolic dysfunction-associated steatotic liver disease (MASLD).

The presentation, titled "Effect of Pemvidutide, a GLP-1/Glucagon Dual Receptor Agonist, on Plasma Lipidomic Profiles in Subjects with Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)," will be given by Dr. Sarah K. Browne on Friday, November 15, 2024, at 1:00 pm PST. Altimmune has also completed enrollment in a Phase 2b efficacy trial of pemvidutide in patients with biopsy-confirmed F2/F3 MASH, with topline data expected in Q2 2025.

Altimmune (Nasdaq: ALT) ha annunciato che nuovi dati sul profilo lipidomico dei soggetti trattati con pemvidutide saranno presentati al The Liver Meeting® 2024 dell'American Association for the Study of Liver Diseases (AASLD) a San Diego, CA, dal 15 al 19 novembre 2024. I dati mostrano riduzioni in più classi di lipidi aterogeni e cardio-infiammatori da uno studio randomizzato, in doppio cieco, controllato con placebo di fase 1b su soggetti con malattia epatica steatosica associata a disfunzione metabolica (MASLD).

La presentazione, intitolata "Effetto di Pemvidutide, un Agonista Doppio del Recettore GLP-1/Glucagone, sui Profili Lipidomici Plasmi nei Soggetti con Malattia Epatica Steatosica Associata a Disfunzione Metabolica (MASLD)," sarà tenuta dalla Dott.ssa Sarah K. Browne venerdì 15 novembre 2024, alle 13:00 PST. Altimmune ha anche completato l'arruolamento in un trial di efficacia di fase 2b di pemvidutide in pazienti con MASH F2/F3 confermata da biopsia, con dati preliminari attesi nel secondo trimestre del 2025.

Altimmune (Nasdaq: ALT) anunció que nuevos datos sobre el perfil lipidómico de los sujetos tratados con pemvidutide se presentarán en The Liver Meeting® 2024 de la American Association for the Study of Liver Diseases (AASLD) en San Diego, CA, del 15 al 19 de noviembre de 2024. Los datos muestran reducciones en múltiples clases de lípidos aterogénicos y cardio-inflamatorios de un estudio aleatorio, doble ciego, controlado con placebo de fase 1b en sujetos con enfermedad del hígado graso asociada a disfunción metabólica (MASLD).

La presentación, titulada "Efecto de Pemvidutide, un Agonista Doble del Receptor GLP-1/Glucagón, sobre los Perfiles Lipidómicos Plasmáticos en Sujetos con Enfermedad Hepática Grasa Asociada a Disfunción Metabólica (MASLD)," será realizada por la Dra. Sarah K. Browne el viernes 15 de noviembre de 2024, a la 1:00 pm PST. Altimmune también ha completado la inscripción en un ensayo de eficacia de fase 2b de pemvidutide en pacientes con MASH F2/F3 confirmada por biopsia, con datos preliminares esperados para el segundo trimestre de 2025.

Altimmune (Nasdaq: ALT)는 pemvidutide로 치료받은 대상의 지질 프로필에 대한 새로운 데이터를 발표할 예정이며, 이 데이터는 2024년 11월 15일부터 19일까지 샌디에고, CA에서 열리는 미국 간 질환 연구 협회(AASLD)의 The Liver Meeting® 2024에서 발표됩니다. 이 데이터는 대사 기능 장애가 관련된 지방간 질환(MASLD)을 가진 피험자를 대상으로 한 12주 간의 1b상 임상시험에서 동맥경화성 및 심혈관 염증성 지질의 여러 클래스에서의 감소를 보여줍니다.

이번 발표는 "대사 기능 장애가 관련된 지방간 질환(MASLD) 환자에서 Pemvidutide(GLP-1/글루카곤 이중 수용체 작용제)가 혈장 지질 프로필에 미치는 영향"이라는 제목으로 Dr. Sarah K. Browne이 2024년 11월 15일 금요일 오후 1시 PST에 진행합니다. Altimmune은 또한 생검으로 확인된 F2/F3 MASH 환자를 대상으로 한 2b상 효능 시험이 완료되었으며, 주요 데이터는 2025년 2분기에 예상됩니다.

Altimmune (Nasdaq: ALT) a annoncé que de nouvelles données sur le profil lipidomique des sujets traités par pemvidutide seront présentées lors du The Liver Meeting® 2024 de l'American Association for the Study of Liver Diseases (AASLD) à San Diego, CA, du 15 au 19 novembre 2024. Les données montrent des réductions dans plusieurs classes de lipides athérogènes et cardio-inflammatoires issues d'une étude de phase 1b randomisée, contrôlée par placebo, sur des sujets souffrant de maladie hépatique grasse associée à une dysfonction métabolique (MASLD).

La présentation, intitulée "Effet de Pemvidutide, un agoniste dual des récepteurs GLP-1/glucagon, sur les profils lipidomiques plasmatiques des sujets avec maladie hépatique grasse associée à une dysfonction métabolique (MASLD)," sera donnée par le Dr. Sarah K. Browne le vendredi 15 novembre 2024, à 13h00 PST. Altimmune a également complété l'enregistrement dans un essai d'efficacité de phase 2b de pemvidutide chez des patients avec MASH F2/F3 confirmé par biopsie, avec des données préliminaires attendues pour le deuxième trimestre de 2025.

Altimmune (Nasdaq: ALT) gab bekannt, dass neue Daten zum lipidomischen Profil von mit pemvidutide behandelten Probanden auf The Liver Meeting® 2024 der American Association for the Study of Liver Diseases (AASLD) in San Diego, Kalifornien, vom 15. bis 19. November 2024 präsentiert werden. Die Daten zeigen Reduktionen in mehreren Klassen von atherogenen und kardiovaskulär-entzündlichen Lipiden aus einer 12-wöchigen, randomisierten, placebokontrollierten Phase-1b-Studie bei Probanden mit metabolisch bedingter fettiger Lebererkrankung (MASLD).

Die Präsentation mit dem Titel "Wirkung von Pemvidutide, einem Dual-Agonisten des GLP-1/Glukagon-Rezeptors, auf lipidomisches Profil im Plasma bei Probanden mit metabolisch bedingter fettiger Lebererkrankung (MASLD)" wird am Freitag, den 15. November 2024, um 13:00 Uhr PST von Dr. Sarah K. Browne gehalten. Altimmune hat zudem die Rekrutierung in einer Phase-2b-Effizienzstudie von Pemvidutide bei Patienten mit biopsiebestätigtem F2/F3 MASH abgeschlossen, und die ersten Ergebnisse werden im 2. Quartal 2025 erwartet.

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GAITHERSBURG, Md., Oct. 15, 2024 (GLOBE NEWSWIRE) -- Altimmune, Inc. (Nasdaq: ALT), a clinical-stage biopharmaceutical company, today announced that new data showing reductions of multiple classes of atherogenic and cardio-inflammatory lipids in subjects treated with pemvidutide will be presented in a poster session at The Liver Meeting® 2024 of the American Association for the Study of Liver Diseases (AASLD) in San Diego, CA taking place November 15-19, 2024. The data were derived from Altimmune’s 12-week Phase 1b randomized, placebo-controlled study in subjects with metabolic dysfunction-associated steatotic liver disease (MASLD), a precursor to the more serious metabolic dysfunction-associated steatohepatitis (MASH). The Company has completed enrollment in a Phase 2b efficacy trial of pemvidutide in patients with biopsy-confirmed F2/F3 MASH, with topline data expected in the second quarter of 2025.

Details of the presentation are as follows:

Title:Effect of Pemvidutide, a GLP-1/Glucagon Dual Receptor Agonist, on Plasma Lipidomic Profiles in Subjects with Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)
Presenter:Dr. Sarah K. Browne, Vice President, Clinical Development, Altimmune
Date/Time:Friday, November 15, 2024, at 1:00 pm PST
  

The poster will be available on the Events section of the Altimmune website at the time of the presentation.

About Pemvidutide 

Pemvidutide is a novel, investigational, peptide-based GLP-1/glucagon dual receptor agonist in development for the treatment of obesity and MASH. Activation of the GLP-1 and glucagon receptors is believed to mimic the complementary effects of diet and exercise on weight loss, with GLP-1 suppressing appetite and glucagon increasing energy expenditure. Glucagon is also recognized as having direct effects on hepatic fat metabolism, which is believed to lead to rapid reductions in levels of liver fat and serum lipids. In clinical trials to date, once-weekly pemvidutide has demonstrated compelling weight loss, robust reductions in triglycerides, LDL cholesterol, liver fat content and blood pressure, while preserving lean mass. The U.S. FDA has granted Fast Track designation to pemvidutide for the treatment of MASH. Pemvidutide recently completed the MOMENTUM Phase 2 obesity trial and is being studied in the ongoing IMPACT Phase 2b MASH trial. 

About Altimmune

Altimmune is a clinical-stage biopharmaceutical company focused on developing innovative next-generation peptide-based therapeutics. The Company is developing pemvidutide, a GLP-1/glucagon dual receptor agonist for the treatment of obesity and MASH. For more information, please visit www.altimmune.com.

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Company Contact:
Vipin Garg
President and Chief Executive Officer
Phone: 240-654-1450
ir@altimmune.com

Media Contact:
Danielle Cantey
Inizio Evoke, Biotech
Phone: 619-826-4657
Danielle.cantey@inizioevoke.com

Investor Contacts:
Lee Roth
Burns McClellan
Phone: 646-382-3403
lroth@burnsmc.com

Julia Weilman
Burns McClellan
Phone: 646-732-4443
jweilman@burnsmc.com

This press release was published by a CLEAR® Verified individual.


FAQ

What new data will Altimmune (ALT) present at The Liver Meeting® 2024?

Altimmune will present new data showing reductions of multiple classes of atherogenic and cardio-inflammatory lipids in subjects treated with pemvidutide. This data comes from a 12-week Phase 1b study in subjects with metabolic dysfunction-associated steatotic liver disease (MASLD).

When and where will Altimmune (ALT) present its pemvidutide data at The Liver Meeting® 2024?

Altimmune will present the pemvidutide data on Friday, November 15, 2024, at 1:00 pm PST during The Liver Meeting® 2024 in San Diego, CA, which takes place from November 15-19, 2024.

What is the title of Altimmune's (ALT) presentation at The Liver Meeting® 2024?

The title of Altimmune's presentation is "Effect of Pemvidutide, a GLP-1/Glucagon Dual Receptor Agonist, on Plasma Lipidomic Profiles in Subjects with Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)".

What is the current status of Altimmune's (ALT) Phase 2b trial for pemvidutide?

Altimmune has completed enrollment in a Phase 2b efficacy trial of pemvidutide in patients with biopsy-confirmed F2/F3 MASH. Topline data from this trial is expected in the second quarter of 2025.

Altimmune, Inc.

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