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Fortrea Lança AI Innovation Studio para Galvanizar Tecnologia e Soluções Humanas para Aprimoramento da Entrega de Ensaios Clínicos

DURHAM, N.C., June 28, 2024 (GLOBE NEWSWIRE) — A Fortrea (Nasdaq: FTRE), uma organização líder global de pesquisa por contrato (CRO), anunciou hoje o lançamento do seu AI Innovation Studio, sinalizando um investimento estratégico na reformulação da execução de ensaios clínicos hoje e no futuro.

O Studio desenvolverá e implantará tecnologias de IA e aprendizado de máquina (ML) para impulsionar a velocidade, agilidade, qualidade e segurança aprimorada do paciente no processo de pesquisa clínica, equipando e capacitando as pessoas a se concentrarem no elemento humano tão essencial nos ensaios clínicos.

“Pacientes de todo o mundo estão esperando por novos tratamentos que irão mudar suas vidas. Com a IA, agora temos o poder – e a obrigação – de ajudar a fornecer soluções para esses pacientes mais rapidamente”, disse o diretor de informações da Fortrea, Alejandro Martinez Galindo.

“O AI Innovation Studio da Fortrea viabilizará os recursos tecnológicos aprimorados que permitirão que os sistemas habilitados para IA executem processos de ponta – como simulações de testes, análises preditivas e reconhecimento de padrões – além de tarefas repetitivas, administrativas e fáceis de operar. Isso permite que as pessoas possam contribuir com a criatividade humana e a conexão com o ensaio clínico futuro e se concentrar no que é o mais importante: o paciente.”

O AI Innovation Studio da Fortrea visa:

  • Estabelecer parcerias em toda a Fortrea e com nossos clientes para fornecimento de soluções tecnológicas para estratégias de inovação sob medida para locais e patrocinadores;
  • Desenvolver inovações tecnológicas novas e inovadoras que aprimorem holisticamente a entrega de ensaios clínicos para patrocinadores, locais, pacientes e nossas equipes; e
  • Apoiar a infraestrutura e as operações existentes com tecnologia aprimorada para viabilizar novas e aprimoradas maneiras de trabalho e criação das melhores experiências de usuário da categoria.

As tecnologias em desenvolvimento no Studio incluem coleta de dados habilitada para smartphones; grandes modelos de linguagens especializados para compreensão e geração de texto; IA simbólica com lógica de valor real (ou seja, criação de lógica de decisão com cenários e dados do mundo real); realidade mista e inteligência aumentada; mineração avançada de dados e análise preditiva; e geminação digital.

A aplicação estratégica dessas tecnologias deve resultar em avanços significativos no recrutamento e retenção de pacientes, criação/otimização de protocolos, monitoramento de qualidade baseado em risco e velocidade e qualidade gerais da entrega. Essas tecnologias também podem proporcionar uma melhor experiência para o paciente e maior produtividade para os clientes, locais e funcionários da Fortrea.

Os desenvolvimentos do AI Innovation Studio serão fundamentais para a plataforma de tecnologia clínica da Fortrea que está sendo projetada para integrar a tecnologia de ensaios clínicos em uma experiência de nível de consumidor, independente de localização, omnicanal e baseada em persona, acessível por meio de uma única tela.

“A Fortrea está focada em uma visão de futuro da indústria de CRO que nos permite criar Voltados para o futuro e Não para o passado”, disse Brian Dolan, Vice–Presidente de Inteligência Artificial e Aprendizado de Máquina. “Estamos sendo bem cautelosos e levando em consideração o desenvolvimento e a implantação responsáveis e éticos da IA, priorizando fazer a coisa certa pelas razões certas e protegendo a segurança e a privacidade do paciente e a propriedade intelectual dos nossos clientes.”

Sobre a Fortrea
A Fortrea (Nasdaq: FTRE) é fornecedora líder global de soluções para o desenvolvimento clínico para a indústria de ciências da vida. Fazemos parcerias com grandes e emergentes empresas biofarmacêuticas, de biotecnologia, de dispositivos médicos e de diagnóstico para impulsionar a inovação na saúde que acelera terapias que mudam a vida dos pacientes. A Fortrea fornece gerenciamento de testes clínicos de fase I–IV, farmacologia clínica e serviços de consultoria. As soluções da Fortrea utilizam suas três décadas de experiência abrangendo mais de 20 áreas terapêuticas, sua dedicação ao rigor científico, insights excepcionais e uma forte rede de pesquisadores. Nossa equipe talentosa e diversificada que trabalha em mais de 90 países é dimensionada para fornecer soluções focadas e ágeis para clientes de todo o mundo. Saiba mais sobre como a Fortrea está se tornando uma força transformadora de pipeline para pacientes na Fortrea.com e siga–nos no LinkedIn e X (antigo Twitter).

Contatos da Fortrea:
Hima Inguva (Investidores) – 877–495–0816, hima.inguva@fortrea.com
Jennifer Minx (Mídia) – 919–410–4195, media@fortrea.com
Kate Dillon (Mídia) – 646–818–9115, kdillon@prosek.com


GLOBENEWSWIRE (Distribution ID 9170901)

Fortrea Launches AI Innovation Studio to Galvanize Technology and Human Solutions to Improve Clinical Trial Delivery

DURHAM, N.C., June 27, 2024 (GLOBE NEWSWIRE) — Fortrea (Nasdaq: FTRE), a leading global contract research organization (CRO), today announced the launch of its artificial intelligence (AI) Innovation Studio, signaling a strategic investment in reshaping the execution of clinical trials today and into the future.

The studio will develop and deploy AI and machine learning (ML) technologies to drive speed, agility, quality and enhanced patient safety in the clinical research process by equipping and empowering people to focus on the critical human element of clinical trials.

“Patients around the world are waiting for novel, life–changing treatments. With AI, we now have the power—and the obligation—to help deliver solutions to them faster,” said Fortrea’s Chief Information Officer Alejandro Martinez Galindo.

“Fortrea’s AI Innovation Studio will enable enhanced technological capabilities that will allow AI–enabled systems to perform cutting–edge processes—such as trial simulations, predictive analytics and pattern recognition—as well as repetitive, administrative, ‘machine–friendly tasks’. This frees up people to contribute human creativity and connection to the clinical trial of tomorrow and focus on what counts: the patient.”

Fortrea’s AI Innovation Studio aims to:

  • Partner across Fortrea and with our customers to provide technology solutions for bespoke site and sponsor innovation strategies;
  • Develop net new, greenfield technology innovations that holistically improve the delivery of clinical trials for sponsors, sites, patients and our teams; and
  • Support existing infrastructure and operations with enhanced technology to enable new, improved ways of working and create best–in–class user experiences.

Technologies under development in the studio include smartphone–enabled data collection; specialized large language models for text comprehension and generation; symbolic AI with real–valued logic (i.e., building decision logic using real–world scenarios and data); mixed reality and augmented intelligence; advanced data mining and predictive analytics; and digital twinning.

Strategic application of these technologies is expected to result in meaningful advancements in patient recruitment and retention, protocol creation/optimization, risk–based quality monitoring and overall delivery speed and quality. These technologies can also deliver an improved patient experience and greater productivity for Fortrea customers, sites and employees.

Developments from the AI Innovation Studio will be critical to Fortrea’s clinical technology platform, which is being designed to integrate clinical trial technology into a consumer–grade, location–agnostic, omni–channel, persona–based experience accessible thorough a single screen.

“Fortrea is focused on a future vision of the CRO industry, allowing us to build TO the future rather than FROM the past,” said Brian Dolan, Vice President of Artificial Intelligence & Machine Learning. “We are exercising great care and consideration to the responsible and ethical development and deployment of AI, prioritizing doing the right thing for the right reasons and protecting patient safety and privacy, and the intellectual property of our customers.”

About Fortrea
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, biotechnology, medical device and diagnostic companies to drive healthcare innovation that accelerates life–changing therapies to patients. Fortrea provides phase I–IV clinical trial management, clinical pharmacology and consulting services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com and follow us on LinkedIn and X (formerly Twitter).

Fortrea Contacts:
Hima Inguva (Investors) – 877–495–0816, hima.inguva@fortrea.com
Jennifer Minx (Media) – 919–410–4195, media@fortrea.com
Kate Dillon (Media) – 646–818–9115, kdillon@prosek.com


GLOBENEWSWIRE (Distribution ID 9170022)

OPEN Health and fusion announce partnership to deliver AI-powered healthcare communications

London, June 24, 2024 (GLOBE NEWSWIRE) — June 24, 2024, London, UK – OPEN Health, a pre–eminent global provider of scientific communications, HEOR and market access, patient engagement, and consulting, today announced a partnership with fusion, an innovative artificial intelligence (AI) and machine learning (ML) solutions provider that will work exclusively with OPEN Health. This alliance will see fusion's market–leading AI capabilities deployed across OPEN Health's extensive global client base, which includes 49 of the top 50 pharmaceutical companies.

Mary McGregor, Founder of fusion, commented, “OPEN Health provides an unrivalled platform to expand the AI agenda globally in our sector. Our longstanding relationship with OPEN Health leadership facilitated early conversations, enabling us to quickly market–test joint solutions, which led to a swift and unanimous decision to formalize this collaboration. This partnership empowers us to redefine the boundaries of what AI can accomplish in healthcare.”

Margot Hannah,  Chief Executive Officer of Scientific Communications at OPEN Health, expressed her enthusiasm for the partnership: “We immediately recognized the need to expand our capabilities and started a dialog with fusion about an exclusive partnership to provide pioneering solutions that integrate OPEN Health’s capabilities with fusion’s cutting–edge expertise in AI and ML. Fusion’s expertise in this area is unparalleled, and we are excited about the possibilities this partnership brings for our clients.”

Steve Duryee, Chief Operating and Transformation Officer at OPEN Health, added, “We are committed to harnessing the power of cutting–edge technologies, including AI, ML, robotic process automation, and data analytics, to drive higher value and improved outcomes for our clients. With the recent launch of our Solutions Innovation Center, and the addition of fusion to our extended team of elite–level technology partners, we are now in the pole position to deliver the most innovative, technologically advanced solutions to our biopharmaceutical partners.”

By integrating with fusion’s advanced technology, OPEN Health underscores its commitment to leading the AI agenda with socially beneficial innovations to drive innovation and efficiency for clients. Contact OPEN Health to set up an interactive demonstration at www.openhealthgroup.com/contact–us.

About OPEN Health
OPEN Health unites world–class scientific, strategic, and creative expertise to solve complex challenges for global biopharma. We are a flexible, global organization, creating high–performing strategic partnerships with our clients. We embrace our different perspectives and strengths to deliver innovative solutions that have a positive impact on commercial and patient outcomes. OPEN Health unlocks possibilities across consulting, HEOR and market access, scientific communications, and patient engagement. To learn more, visit www.openhealthgroup.com.

About fusion
fusion specializes in delivering AI and ML solutions. Known for its advanced technology and innovative approach, fusion aims to transform the pharmaceutical industry by integrating AI–first solutions. To learn more, visit www.fusionagency.solutions.

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GLOBENEWSWIRE (Distribution ID 9157597)

Allecra Therapeutics and Acino Sign Exclusive Licensing and Supply Agreement for Allecra’s Novel Antibiotic EXBLIFEP® in Gulf Cooperation Council countries and South Africa

Saint–Louis, France and Weil am Rhein, Germany and Zurich, Switzerland, June 24, 2024 (GLOBE NEWSWIRE) — Allecra Therapeutics (“Allecra”) and Acino today announced the signing of an exclusive licensing agreement under which Acino gains the rights to commercialise Allecra’s antibiotic drug EXBLIFEP® (cefepime/enmetazobactam) within the Republic of South Africa and the member states of the GCC alliance, which includes Bahrain, Kuwait, Oman, Qatar, Saudi Arabia, and the United Arab Emirates, effective from 12 June 2024. In addition, the companies have signed a supply agreement under which Allecra will supply the cefepime/enmetazobactam finished product in the above territories.

“Acino has established itself as a leader in South Africa and the GCC region. They are an ideal partner to support us as we build towards commercialisation of EXBLIFEP® following our regulatory approvals in the US and EU,” stated Andreas Kranzusch, Chief Financial Officer and Managing Director at Allecra Therapeutics. “This agreement reflects the understanding that there remains a significant global need to address the dangerous increase of resistance to standard–of–care antibiotics, and we look forward to working with Acino to address this.”

“At Acino, we are dedicated to providing novel healthcare solutions to physicians and patients, aiming to alleviate the health burden in emerging markets. We are incredibly excited to partner with Allecra to offer access to this innovative product in two key geographic regions and, potentially, beyond,” said Andrew Bird, CEO (ai) at Acino. “We are committed to expediting the registration process in these designated markets to ensure hospitals’ swift access to EXBLIFEP® as they continue to fight against high–risk infectious diseases in patients.”

About EXBLIFEP® (cefepime/enmetazobactam)

EXBLIFEP® is an intravenous antibiotic fixed–dose combination of enmetazobactam, a novel extended–spectrum β–lactamase inhibitor belonging to the penicillanic acid sulfone class, with the fourth–generation cephalosporin cefepime. Enmetazobactam has been shown to restore the efficacy of cefepime against some multi–drug resistant bacteria, including ESBL–producing pathogens alone or in combination with some resistant β–lactamase mutations as OXA–48 or AmpC, which are increasing in Europe and for which there are few therapeutic alternatives.

EXBLIFEP® demonstrated statistically significant superior overall treatment success in Allecra’s pivotal Phase III ALLIUM trial, which compared 1034 randomized patients receiving either cefepime 2 g/enmetazobactam 0.5 g or piperacillin 4 g/tazobactam 0.5 g every 8 h as 2 h continuous intravenous infusion in a multi–centre, randomized, controlled, double–blind, global study in 112 sites within nineteen countries.

In February 2024, the U.S. Food and Drug Administration (FDA) approved EXBLIFEP® as a treatment for complicated urinary tract infections (cUTI), including pyelonephritis, in patients 18 years and older. In March 2024 the European Commission (EC) granted marketing authorisation for EXBLIFEP® for the treatment of adult patients with cUTI, including pyelonephritis; hospital–acquired pneumonia (HAP), including ventilator–associated pneumonia (VAP); and bacteraemia that occurs in association with, or is suspected to be associated with any of the infections listed previously.

About Allecra Therapeutics

Allecra Therapeutics, founded in 2013, is a private, clinical–stage biopharmaceutical company developing novel therapies to combat antibiotic resistance by overcoming emergent resistance mechanisms. Lead product candidate EXBLIFEP® (cefepime/enmetazobactam), has successfully completed a randomized, controlled, double–blind, global Phase 3 trial compared to standard of care in patients with complicated urinary tract infections (cUTIs). Based on these results, the company has received FDA marketing approval in the U.S. and announced approval in the European Union for EXBLIFEP® earlier this year.

Allecra has significant patent protection covering proprietary enmetazobactam in major territories. Allecra’s investors include Forbion, Andera Partners, Delos Capital, Xeraya Capital, EMBL Ventures, and BioMedPartners. Allecra’s wholly owned French subsidiary is a beneficiary of financial support from Bpifrance and the Région Alsace. Please visit www.allecra.com for further information.

About Acino

Acino is a Swiss pharmaceutical company headquartered in Zurich with a clear focus on selected markets in the Middle East, Africa, Ukraine, the CIS Region, and Latin America. We deliver quality pharmaceuticals to promote affordable healthcare in these emerging markets and leverage our high–quality pharmaceutical manufacturing capabilities and network to supply leading companies through contract manufacturing and out–licensing. For more information, please visit www.acino.swiss.

Acino is part of Arcera, a global company in the life sciences sector headquartered in Abu Dhabi, United Arab Emirates. Arcera was established by ADQ, an Abu Dhabi–based investment and holding company, to build a global life sciences powerhouse poised to make significant contributions to realising the UAE’s aspiration to emerge as a frontrunner in science and technology. To learn more about Arcera, please visit www.arceralifesciences.com.

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GLOBENEWSWIRE (Distribution ID 9157528)

Adalvo erhält erste Generika-Zulassung in der EU für Liraglutid-Fertigpen

SAN ĠWANN, Malta, June 17, 2024 (GLOBE NEWSWIRE) — Adalvo gibt die erfolgreiche DCP–Zulassung für Liraglutid–Fertigpens und damit die erste Generika–Zulassung in der EU bekannt.

Als Bioäquivalent zu Victoza®, einem Fertigpen für die Behandlung von Typ–2–Diabetes, erzielte das Peptid–Präparat laut IQVIA im Jahr 2023 einen weltweiten Umsatz von mehr als 4,8 Mrd. US–Dollar.

Die erfolgreiche Entwicklung von Liraglutid verdeutlicht die Kompetenz von Adalvo als Anbieter eines vielfältigen und umfassenden Diabetes–Portfolios, das sowohl komplexe Peptid–Präparate zur Injektion als auch niedermolekulare Medikamente zur oralen Einnahme umfasst.

Die Verpflichtung von Adalvo zur Bereitstellung qualitativ hochwertiger, differenzierter Produkte bei gleichzeitiger Bewältigung komplexer Produktionsabläufe stärkt die Position des Unternehmens als zuverlässiger Marktführer in der Pharmabranche.

Klicken Sie hier, um das Diabetes–Portfolio von Adalvo anzusehen

Für Adalvo gibt es keine halben Sachen – der Erfolg steht immer im Fokus. Das Unternehmen hat sich zum Ziel gesetzt, schneller und stärker als seine Wettbewerber zu sein und seine Vision mit einem erfolgreichen Team umzusetzen.

Adalvo verpflichtet sich im Rahmen seiner Geschäftstätigkeit zur Einhaltung höchster Qualitätsstandards und freut sich darauf, auch weiterhin innovative Lösungen für das Gesundheitswesen zur weltweiten Verbesserung der Lebensqualität von Patienten bereitzustellen.

Über Adalvo

Adalvo ist ein weltweit tätiges Pharmaunternehmen und eines der führenden B2B–Pharmaunternehmen in Europa mit Handelspartnerschaften in mehr als 130 Ländern und für über 140 Handelspartner weltweit. Das erklärte Ziel des Unternehmens ist die weltweite Verbesserung der Lebensqualität von Patienten. Grundlage dafür sind unser intelligentes Kooperationsnetzwerk und die Verpflichtung, unseren Partnern differenzierte Produkte und Dienstleistungen von höchster Qualität bereitzustellen.

Besonders stolz ist Adalvo auf seine Möglichkeiten, Partner bei der Erreichung ihrer Ziele, beispielsweise der Steigerung von Umsätzen oder Erschließung neuer Märkte, zu unterstützen. Das Unternehmen setzt sich unermüdlich für herausragende Leistungen ein, getragen von einer tief verwurzelten Leidenschaft dafür, neue Maßstäbe für ihre Partner zu setzen.

Die zielgerichtete Unternehmenskultur verpflichtet sich der weltweiten Verbesserung der Lebensqualität von Patienten. Das dynamische Führungsteam von Adalvo verfügt über umfangreiche Erfahrungen und Branchenkenntnisse, die zum Erfolg des Unternehmens als zuverlässiger globaler Partner in der Branche beigetragen haben.

Kontakt: Gabrielle Cassar, gabrielle.cassar@adalvo.com

Ein Foto zu dieser Mitteilung finden Sie unter https://www.globenewswire.com/NewsRoom/AttachmentNg/e1e895aa–f689–4215–a1f8–25285851af9d


GLOBENEWSWIRE (Distribution ID 1000966644)

Adalvo obtient la première approbation générique de l’UE pour son stylo prérempli de liraglutide

SAN ĠWANN, Malte, 17 juin 2024 (GLOBE NEWSWIRE) — Adalvo annonce l’approbation par procédure décentralisée de son stylo prérempli de liraglutide, soit la toute première approbation générique dans l’UE.

En tant que version bio–équivalente du stylo prérempli Victoza®, indiqué pour le traitement du diabète de type 2, ce médicament peptidique a affiché des ventes mondiales supérieures à 4,8 milliards de dollars en 2023, comme le signale IQVIA.

Le développement réussi du liraglutide met en évidence la capacité d’Adalvo à proposer une gamme diversifiée et complète de traitements pour le diabète, intégrant à la fois des peptides complexes injectables et des traitements oraux à petites molécules.

L’engagement d’Adalvo à fournir un accès à des produits différenciés de haute qualité tout en en maîtrisant les enjeux de fabrication renforce sa position de leader reconnu au sein de l’industrie pharmaceutique.

Cliquez ici pour consulter la gamme de traitements pour le diabète conçue par Adalvo

Chez Adalvo, la notion de demi–mesure n’existe pas. À ce titre, les résultats sont toujours au rendez–vous. La mission de la Société est d’être plus rapide et plus performante que ses concurrents, à l’appui d’une équipe motivée au service de sa vision.

Adalvo s’engage à maintenir les normes d’excellence les plus strictes dans toutes ses activités et entend continuer à proposer des solutions de soins de santé novatrices qui apportent des changements positifs dans la vie des patients du monde entier.

À propos d’Adalvo

Adalvo est une entreprise pharmaceutique d’envergure mondiale et figure parmi les principales entreprises pharmaceutiques B2B d’Europe. Ses partenariats commerciaux sont actifs dans plus de 130 pays, à l’appui de plus de 140 partenaires commerciaux à l’échelle planétaire. L’objectif déclaré de l’entreprise vise l’amélioration de la vie des patients du monde entier au moyen d’un réseau de collaboration intelligent et d’un engagement à fournir des produits et services différenciés de la plus haute qualité à ses partenaires.

Adalvo est fière de sa capacité à accompagner ses partenaires dans la réalisation de leurs objectifs, qu’il s’agisse de relever leur chiffre d’affaires ou de conquérir de nouveaux marchés. Animée par un puissant désir d’apporter des résultats concrets à ses partenaires, Adalvo s’efforce sans relâche d’atteindre l’excellence dans toutes ses activités.

Grâce à sa culture axée sur les objectifs, l’entreprise s’engage à améliorer la vie des patients du monde entier. Son équipe de direction dynamique apporte une expérience et un savoir–faire industriels considérables ayant contribué à faire de l’entreprise un partenaire mondial fiable dans le secteur.

Contacts : Gabrielle Cassar, gabrielle.cassar@adalvo.com

Une photo annexée à ce communiqué est disponible sur https://www.globenewswire.com/NewsRoom/AttachmentNg/e1e895aa–f689–4215–a1f8–25285851af9d


GLOBENEWSWIRE (Distribution ID 1000966644)

Adalvo obtém primeira aprovação genérica da UE para caneta pré-cheia com liraglutida

SAN ĠWANN, Malta, June 17, 2024 (GLOBE NEWSWIRE) — Adalvo anuncia a aprovação bem–sucedida do DCP para a caneta pré–cheia com liraglutida, marcando–a como a primeira aprovação genérica na UE.

Como uma versão bioequivalente da caneta pré–cheia Victoza®, indicada para o tratamento do diabetes tipo 2, este medicamento peptídico alcançou vendas globais superiores a US$ 4,8 bilhões em 2023, conforme divulgado pela IQVIA.

O desenvolvimento bem–sucedido do liraglutida destaca a capacidade da Adalvo de oferecer um portfólio diversificado e abrangente para diabetes, abrangendo tanto injetáveis de peptídeos complexos quanto tratamentos orais de moléculas pequenas.

O compromisso da Adalvo em fornecer acesso a produtos diferenciados de alta qualidade e, ao mesmo tempo, navegar pelas complexidades de fabricação, reforça a posição da empresa como líder confiável na indústria farmacêutica.

Clique aqui para ver o portfólio de diabetes da Adalvo

Na Adalvo, não há meias medidas – eles sempre atingem o objetivo. A sua missão é ser mais rápida e mais forte que os seus concorrentes, promovendo sua visão com uma equipe vencedora.

A Adalvo tem o compromisso de manter os mais altos padrões de excelência em todos os seus empreendimentos e espera continuar a fornecer soluções de saúde inovadoras que façam a diferença na vida dos pacientes em todo o mundo.

Sobre a Adalvo

A Adalvo é uma empresa farmacêutica global e uma das empresas farmacêuticas B2B líderes na Europa, com parcerias comerciais em mais de 130 países e mais de 140 parceiros comerciais em todo o mundo. O objetivo declarado da empresa é fazer a diferença para os pacientes em todo o mundo, motivado por nossa rede de colaboração inteligente e pelo compromisso de fornecer produtos e serviços diferenciados da mais alta qualidade aos nossos parceiros.

A Adalvo se orgulha de sua capacidade de ajudar os parceiros a atingir suas metas, seja para aumentar a receita ou entrar em novos mercados. Busca incansavelmente a excelência em todos os seus empreendimentos, movida por uma paixão profundamente enraizada por fazer a diferença para os parceiros.

A cultura orientada para o propósito da empresa está comprometida em melhorar a vida dos pacientes em todo o mundo. A equipe de liderança dinâmica da Adalvo traz uma experiência significativa e conhecimento do setor, o que ajudou a estabelecer a empresa como um parceiro global confiável no setor.

Contatos: Gabrielle Cassar, gabrielle.cassar@adalvo.com

Uma foto que acompanha este anúncio está disponível em https://www.globenewswire.com/NewsRoom/AttachmentNg/e1e895aa–f689–4215–a1f8–25285851af9d


GLOBENEWSWIRE (Distribution ID 1000966644)

From Awareness to Action on Global Fatty Liver Day

Global Liver Institute Unites the Field in Times of Name Changes and New Treatments

WASHINGTON, June 13, 2024 (GLOBE NEWSWIRE) — Today marks the seventh annual Global Fatty Liver Day (formerly International NASH Day), led by Global Liver Institute (GLI) with the theme “Act Now, Screen Today.” This campaign underscores the crucial need for early identification and treatment of fatty liver disease to prevent its progression to chronic liver disease, cirrhosis, or cancer.

Fatty liver disease is now estimated to affect 1 in 3 adults worldwide, and its prevalence is increasing. Fatty liver disease during childhood, once unheard of, is also on the rise. Early detection and timely intervention, whether through lifestyle changes or medical treatments, are essential in stopping and even reversing the progression of the disease. “Act Now, Screen Today'' emphasizes that liver health is achievable, but action must begin immediately. Across the globe, partners are driving awareness and educational efforts and ensuring broader access to essential screenings and care.

Global Fatty Liver Day, observed annually on the second Thursday of June, is a rallying cry for collective action to address the growing prevalence of fatty liver disease, the most common liver disease worldwide. “Act Now, Screen Today” reminds everyone that liver health is within reach. Here are specific actions you can take today:

  • Take advantage of liver health screening events happening globally to get assessed for fatty liver disease or schedule a check–up with your doctor, especially if you are managing closely associated metabolic conditions like obesity or diabetes
  • Increase physical activity, as maintaining an active lifestyle can improve liver health
  • Learn about fatty liver disease and its risk factors to take proactive steps towards prevention and management yourself or learn more about the latest research and guidelines for your patients.

With a robust pipeline of pharmaceutical treatments that address diverse mechanisms of action in progress, it is important to identify individuals’ position within the progression of fatty liver disease so that they are poised to receive the most appropriate care possible. Notably, pharmaceutical treatments are available (for certain groups with advanced disease) in two countries, the United States (resmetirom) and India (saroglitazar).

“As a community, we stand at a critical time for the broader global health system to act now to support patients,” shares Donna R. Cryer, JD, Founder and CEO of GLI. “As pharmaceutical treatment options gain approval in different geographies, health payers and systems must listen to the call from global advocates and not place undue obstacles to care – whether that be required biopsy, ambiguous lifestyle requirements, or other hurdles – so that patients are able to access the care they require, no matter who or where they are.”

Recognizing the importance of early detection, a diverse range of partners, including healthcare providers, patient advocacy groups, and community organizations, have joined forces to “Act Now, Screen Today” and launch screening events around the world. From Chile to Nigeria to the Netherlands, the Philippines, and beyond, these events aim to raise awareness, provide education, and offer screening services to individuals at risk of fatty liver disease or the providers who care for them. Global Fatty Liver Day activities are driving positive change at the grassroots level.

“Global Fatty Liver Day is an urgent call–to–action to unite our global efforts to confront the scourge of fatty liver disease,” shares Cat Evans, Director of Program Operations at GLI. “We must act now. By working together, we have the power to create significant change in preventing and managing this pressing health issue through our collaborative efforts.”

Although the challenge of fatty liver disease to the well–being of communities around the globe is great, the power of locally–rooted, collective efforts can turn the tide towards positive change by heightening awareness, equipping people and their healthcare providers with prevention and management tools, expanding understanding of the disease through research, and protecting future liver health through effective policies.

About Global Liver Institute

Global Liver Institute (GLI) is a 501(c)3 nonprofit organization founded in the belief that liver health must take its place on the global public health agenda commensurate with the prevalence and impact of liver illness. GLI promotes innovation, encourages collaboration, and supports the scaling of optimal approaches to help eradicate liver diseases. Operating globally, GLI is committed to solving the problems that matter to liver patients and equipping advocates to improve the lives of individuals and families impacted by liver disease. Follow GLI on Facebook, Instagram, LinkedIn, and YouTube, or visit www.globalliver.org. GLI is the host of Global Fatty Liver Day.

Christine Maalouf 
Global Liver Institute
cmaalouf@globalliver.org


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Adalvo Secures First EU Generic Approval for Liraglutide Pre-Filled Pen

SAN ĠWANN, Malta, June 13, 2024 (GLOBE NEWSWIRE) — Adalvo announces the successful DCP approval for Liraglutide pre–filled pen, marking it as the first generic approval in the EU.

As a bioequivalent version of Victoza® pre–filled pen, indicated for the treatment of type 2 diabetes, this peptide drug achieved global sales exceeding $4.8 billion in 2023, as reported by IQVIA.

The successful development of Liraglutide highlights Adalvo's capability to offer a diverse and comprehensive diabetes portfolio, encompassing both complex peptide injectables and small molecule oral treatments.

Adalvo’s commitment to providing access to high–quality differentiated products while simultaneously navigating manufacturing complexities reinforces Adalvo's position as a trusted leader in the pharmaceutical industry.

Click Here To View Adalvo’s Diabetes Portfolio

At Adalvo, there are no half–measures – they are always on target. Their mission is to be faster and stronger than their competitors, driving their vision forward with a winning team.

Adalvo is committed to maintaining the highest standards of excellence in all their endeavors and looks forward to continuing to deliver innovative healthcare solutions that make a difference in the lives of patients worldwide.

About Adalvo

Adalvo is a global pharmaceutical company, and one of the leading B2B pharmaceutical companies in Europe, with commercial partnerships in more than 130 countries and over 140 commercial partners globally. The company’s declared purpose is to make a difference for patients all over the world, driven by our smart collaboration network and commitment to delivering the highest quality differentiated products and services to our partners.

Adalvo takes pride in their ability to help partners reach their goals – be those increasing revenues or pushing into new markets. Tirelessly strives for excellence in all of its endeavours, driven by a deep–rooted passion for making a difference for partners.

The company’s purpose–driven culture is committed to improving the lives of patients around the world. Adalvo’s dynamic leadership team brings significant experience and industry know–how, which has helped to establish the company as a reliable global partner in the industry.

Contacts: Gabrielle Cassar, gabrielle.cassar@adalvo.com

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/e1e895aa–f689–4215–a1f8–25285851af9d


GLOBENEWSWIRE (Distribution ID 1000966220)

Myriad Genetics Collaborates with GSK to Improve Access to HRD Testing in 9 Countries

SALT LAKE CITY, June 11, 2024 (GLOBE NEWSWIRE) — Myriad Genetics, Inc. (NASDAQ: MYGN), a leader in genetic testing and precision medicine, today announced a collaboration with GSK aimed at improving access to homologous recombination deficiency (HRD) diagnostic testing for high–grade serous ovarian cancer (HGSOC) patients. A new sponsored testing program leveraging Myriad’s MyChoice HRD Plus and MyChoice CDx Plus Tests (collectively referred to as Myriad’s MyChoice Tests) is now available in Argentina, Brazil, Chile, Colombia, Egypt, Netherlands, Saudia Arabia, Singapore, and United Arab Emirates.

HRD testing is an important predictive and prognostic biomarker for patients who have ovarian cancer. Myriad’s MyChoice Tests determine HRD status in women with ovarian cancer. Clinicians can order this test through their local pathology labs and samples are sent to Myriad Genetics.

This collaboration delivers on both companies’ shared commitment to improve care for patients with advanced ovarian cancer by facilitating access to genetic testing and demonstrates a mutual dedication to meeting an unmet need for patients who otherwise may not have access to testing.

“Our collaboration with GSK is an important step forward in providing critical genetic insights that can help clinicians guide more personalized ovarian cancer treatment decisions,” said Patrick Burke, PhD, EVP of Strategy and Innovation, Myriad Genetics. “In the pursuit of advancing healthcare equity, Myriad is committed to extending the reach of our diagnostic solutions, like Myriad’s MyChoice Tests into additional markets to support more targeted patient care based on their genomic profile.”

About Myriad’s MyChoice Test
Myriad’s MyChoice® test is the most comprehensive tumor test for determining HRD status based on the assessment of genomic alterations in genes such as BRCA1 and BRCA2 and Genomic Instability Score (GIS) status using Myriad’s proprietary algorithm.  It enables healthcare professionals to identify patients with advanced ovarian cancer who are more likely to respond to treatment with targeted therapies.

About Myriad Genetics
Myriad Genetics is a leading genetic testing and precision medicine company dedicated to advancing health and well–being for all. Myriad develops and offers genetic tests that help assess the risk of developing disease or disease progression and guide treatment decisions across medical specialties where genetic insights can significantly improve patient care and lower healthcare costs. For more information, visit www.myriad.com. 

Safe Harbor Statement
This press release contains “forward–looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including that this collaboration will increase access to HRD testing and can help clinicians guide more personalized ovarian cancer treatment decisions for patients. These “forward–looking statements” are management’s expectations of future events as of the date hereof and are subject to known and unknown risks and uncertainties that could cause actual results, conditions, and events to differ materially and adversely from those anticipated. Such factors include those risks described in the company’s filings with the U.S. Securities and Exchange Commission, including the company’s Annual Report on Form 10–K filed on February 28, 2024, as well as any updates to those risk factors filed from time to time in the company’s Quarterly Reports on Form 10–Q or Current Reports on Form 8–K. Myriad is not under any obligation, and it expressly disclaims any obligation, to update or alter any forward–looking statements, whether as a result of new information, future events or otherwise except as required by law. 

Investor Contact
Matt Scalo
(801) 584–3532
IR@myriad.com

Media Contact
Glenn Farrell
(385) 318–3718
PR@myriad.com


GLOBENEWSWIRE (Distribution ID 9151576)