
A Hundred Experts Urge Strengthening Early Diagnosis of Pulmonary Hypertension in Latin America
BUSINESS WIRE)--The first Latin American edition of the 'IMPAHCT: International Meeting on Pulmonary Hypertension Clinical Treatment' congress gathered nearly one hundred pulmonology and cardiology experts this past weekend in Panama City. The aim: to reflect on the current state of pulmonary hypertension (PH) in Latin America. Though this serious disease affects only about 1% of the global population, it brings debilitating symptoms and a heightened risk of mortality.
The congress, organized by Ferrer, the pharmaceutical company with the highest B Corp score worldwide, facilitated connections among specialists from various disciplines and regions across Latin America.
'The challenges in Latin America begin with raising awareness among the medical community. We must understand the disease and know how to diagnose it in order to refer patients to specialized centers as soon as possible,' stated Dr. Angelo Valencia, Pediatric Cardiologist and Specialist in Congenital Diseases at the Imbanaco Clinic in Cali, Colombia.
Dr. Valencia also emphasized the importance of promoting early diagnosis of PH, which remains underdiagnosed in much of Latin America: 'The diagnosis of PH relies on measurements obtained through a cardiac catheterization, which, when properly performed in an experienced center, is low-risk and relatively straightforward.'
During the summit, the main causes of delayed diagnosis were discussed, including the non-specific nature of symptoms, a general lack of awareness about the disease among primary care physicians, and limited access to diagnostic tools.
The congress also addressed the real-life burden of the disease on patients, families, and caregivers, and highlighted the role institutions should play. 'While resources are important, decision-makers need to understand that a treated patient can be economically active. With proper treatment, they can continue to contribute socially, economically, professionally, and personally. An untreated patient deteriorates continuously, which becomes a financial burden on institutions,' stressed Dr. Nayeli Zayas, Head of the Cardiopulmonary Department at the National Institute of Cardiology Ignacio Chávez in Mexico.
According to Jorge Candia, Ferrer's Latam Region Director, 'In line with our purpose of using business to fight for social justice, we are proud to contribute to ongoing medical education in Latin America. Thanks to events like IMPAHCT, attendees will return to their countries and share the knowledge gained here, leading to improved prognosis and care for patients with pulmonary hypertension.'
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Business Wire
2 hours ago
- Business Wire
Budweiser Kicks Off New 'Celebration in the Making' Global Platform
LONDON--(BUSINESS WIRE)--Today, Budweiser (Brussel:ABI) (BMV:ANB) (JSE:ANH) (NYSE:BUD) unveils its new global platform 'Celebration in the Making' and full campaign details as the Official Global Beer Sponsor of the FIFA Club World Cup 2025™. This summer, as football supporters around the globe bring their energy to the groundbreaking tournament, Budweiser will be there to elevate celebrations at every stage – from the opening touch to the final whistle, and beyond. To inspire celebrations from the start, Budweiser is officially kicking off the platform with a new film set to an iconic score, and announces the return of its acclaimed 'Bring Home The Bud' campaign to deliver the ultimate prize of free beer for the winning club* and its supporters. Budweiser will also leverage exclusive FIFA-created 'Celebration of the Match' content featuring the top celebrations from each matchday, and has released new LTO tournament-inspired packaging and designs on its products. 'In partnership with FIFA, Budweiser has been celebrating football culture and its legions of fans for nearly 40 years, and we're proud to launch this global platform to match the energy, scale and excitement of this unique competition,' said Richard Oppy, Global President, Premium Company at AB InBev, brewer of Budweiser. 'Whether it's being in a local pub at match kickoff or being in a packed stadium cheering the return of a champion club, Budweiser will be there to ensure every moment of this FIFA Club World Cup feels like an epic celebration in the making.' Bring Home The Bud Budweiser's celebrated 'Bring Home The Bud' campaign first debuted during the FIFA World Cup 2022™ and then again for the FIFA Women's World Cup 2023™, giving fans of those winning countries a celebration fitting of a world champion: free beer for those of a legal drinking age. The 'Bring Home The Bud' football tradition continues this tournament, as the signature Budweiser-branded red beer crates are already making appearances in cities across Brazil, UK, and China to build excitement for the ultimate payoff for the winning club* and its home supporters. Details about how 'Bring Home The Bud' will come to life for the winning club will continue to unfold throughout the tournament. To learn more, visit Unleashing Celebration in the Making Budweiser channels the passion and raw energy of football fans in its new film, 'ThunderBud,' set to AC/DC's legendary 'Thunderstruck.' The spot captures the moment a Budweiser can cracks open in a crowded stadium, unleashing an electrifying anthem that raises fans and players alike toward victory. In a first-of-its-kind integration, Budweiser will celebrate standout moments on the pitch through 'Celebration of the Match' content created by FIFA for each matchday, which Budweiser will amplify across social media. Fans will have the chance to vote online for their favorite highlights — whether it's an unbelievable goal or a game-saving goalkeeper stop — tying the emotional pinnacle of each match to the idea that fans are the ones who power the game. Watch 'ThunderBud' on YouTube, and follow all the 'Celebration of the Match' action across social media at @budweiser and @budfootball on Instagram, Facebook and X during the tournament. The Beer of Celebration Unique for this year's tournament, Budweiser has launched limited-edition LTO packaging at retail for Budweiser and Budweiser Zero with an updated crest and creed, crafted to include bespoke gold elements for FIFA Club World Cup 2025™. Budweiser Zero will keep its same design while featuring FIFA Club World Cup 2025™ branding, now with a white base to signal its no-alcohol badge of honor. As the Official Beer of the FIFA Club World Cup 2025™, Budweiser continues its legacy of championing football and fan passion on the world's biggest stages, elevating celebrations wherever the game is played. About Budweiser Budweiser is a globally iconic lager born from a bold vision. In 1876, founder Adolphus Busch set out to create the United States' first truly national beer brand – brewed to be universally popular and transcend regional tastes. Today, Budweiser is recognized as the world's second most valuable beer brand in Kantar's BrandZ global 2025 rankings, enjoyed in more than 80 countries and brewed with the same unwavering commitment to quality and consistency. Each batch of Budweiser stays true to the same family recipe used by five generations of Busch family brewmasters. Budweiser is a medium-bodied, flavorful, crisp beer with layers of premium American hop aromas, brewed for the perfect balance of flavor and refreshment. Budweiser is made using time-honored methods including "kraeusening" for natural carbonation and Beechwood aging, which results in unparalleled balance and character. About AB InBev Anheuser-Busch InBev (AB InBev) is a publicly traded company (Euronext: ABI) based in Leuven, Belgium, with secondary listings on the Mexico (MEXBOL: ANB) and South Africa (JSE: ANH) stock exchanges and with American Depositary Receipts on the New York Stock Exchange (NYSE: BUD). As a company, we dream big to create a future with more cheers. We are always looking to serve up new ways to meet life's moments, move our industry forward and make a meaningful impact in the world. We are committed to building great brands that stand the test of time and to brewing the best beers using the finest ingredients. Our diverse portfolio of well over 500 beer brands includes global brands Budweiser®, Corona®, Stella Artois® and Michelob Ultra®; multi-country brands Beck's®, Hoegaarden® and Leffe®; and local champions such as Aguila®, Antarctica®, Bud Light®, Brahma®, Cass®, Castle®, Castle Lite®, Cristal®, Harbin®, Jupiler®, Modelo Especial®, Quilmes®, Victoria®, Sedrin®, and Skol®. Our brewing heritage dates back more than 600 years, spanning continents and generations. From our European roots at the Den Hoorn brewery in Leuven, Belgium. To the pioneering spirit of the Anheuser & Co brewery in St. Louis, US. To the creation of the Castle Brewery in South Africa during the Johannesburg gold rush. To Bohemia, the first brewery in Brazil. Geographically diversified with a balanced exposure to developed and developing markets, we leverage the collective strengths of approximately 144 000 colleagues based in nearly 50 countries worldwide. For 2024, AB InBev's reported revenue was 59.8 billion USD (excluding JVs and associates).


Business Wire
3 hours ago
- Business Wire
PIF 與 FIFA 攜手,共同舉辦 FIFA Club World Cup 2025™
蘇黎世 & 沙特阿拉伯利雅得--(BUSINESS WIRE)--(美國商業資訊)-- PIF 與 FIFA 今日宣佈,PIF 成為 FIFA Club World Cup 2025™ 的官方合作夥伴,賽事將於 2025 年 6 月 14 日至 7 月 13 日在美國舉行。 此次合作展現了 PIF 與 FIFA 的共同願景,即透過創造新機遇、推動創新和吸引全球球迷,來實現更廣泛的體育參與。合作將重點關注青少年,為年輕群體創造機遇,助力 FIFA 深化基層足球推廣。 FIFA Club World Cup 2025™ 是球會足球全球舞台上的新篇章,將匯聚來自 FIFA 六大洲足協的冠軍球隊,共計 32 支頂級球會,在美國 11 個城市展開為期一個月的巔峰對決。 FIFA 首席商務官 Romy Gai 表示:「我們非常高興 PIF 成為 FIFA Club World Cup 2025™ 的合作夥伴。我們期待攜手打造這場歷史性的賽事,激勵並凝聚來自世界各地的球迷。」 「首屆 32 隊制 FIFA Club World Cup 的合作夥伴與我們一樣,致力於實現足球真正全球化的願景。他們的支援不僅是賽事成功的關鍵,也為全球球會足球的發展注入強勁動力。」 PIF 企業品牌主管 Mohammed AlSayyad 表示:「PIF 正在透過多項策略合作,在體育領域打造變革性影響,為球員、球迷和主辦城市社區帶來積極和持久的成果。 「繼去年宣佈與 Concacaf 合作以及我們對足球的持續投資後,PIF 始終站在推動全球足球發展的前沿。我們正不斷開拓機遇,加速這項運動在世界範圍內的發展。」 足球在沙特阿拉伯持續轉型中扮演著關鍵角色。作為 FIFA World Cup 2034™ 的主辦國,進一步彰顯了沙特推動全球足球發展、創造新機遇,並讓這項運動的積極影響惠及本國及全球,造福後人。 FIFA Club World Cup 2025™ 將在美國 11 個城市的 12 座球場舉行,賽事共 63 場。決賽將於 7 月 13 日(星期日)在新澤西州的 MetLife Stadium 上演,屆時將誕生新的 FIFA 球會世界冠軍。 所有賽事將在 免費直播,全球球迷可網上同步觀賽。門票及包含門票的觀賽套餐可透過 購買。 關於 PIF PIF 是推動沙特阿拉伯及全球經濟轉型的投資引擎。透過實施 Vision 2030 策略,PIF 在項目、企業和合作夥伴等層面持續投入,推動沙特經濟多元化,促進各領域增長,創造投資與就業新機遇。 作為全球投資者和變革催化劑,PIF 積極與世界各地最具開創性的組織合作,助力其增長,並引進技術與知識,推動構建未來產業生態系統。 自 2017 年以來,PIF 已設立 103 家公司,並透過在沙特公共及私營領域的策略投資與合作,引領經濟可持續發展轉型。PIF 正為本地和國際合作夥伴投資沙特的經濟和社會轉型奠定基礎。 免責聲明:本公告之原文版本乃官方授權版本。譯文僅供方便瞭解之用,煩請參照原文,原文版本乃唯一具法律效力之版本。


Business Wire
5 hours ago
- Business Wire
RAD 2025: Long-Term Data on Nemluvio ® (nemolizumab) Demonstrate its Favorable Safety Profile and Sustained and Increased Improvements in Itch and Skin Lesions in Patients With Atopic Dermatitis up to Two Years
ZUG, Switzerland--(BUSINESS WIRE)--Galderma (SIX: GALD) today announced two-year data from a new interim analysis of a long-term extension study investigating the safety and efficacy of Nemluvio in moderate-to-severe atopic dermatitis. The data show that Nemluvio is well tolerated, with no new safety signals identified, reinforcing its rapid onset of action and demonstrating sustained and increased improvements in symptoms including itch and skin lesions with prolonged treatment up to two years. 1 These data will be presented in a late-breaker abstract at the Revolutionizing Atopic Dermatitis (RAD) Conference, taking place from June 6-7, 2025. BALDO SCASSELLATI SFORZOLINI, M.D., PHD. GALDERMA Expand Atopic dermatitis affects more than 230 million people worldwide. 3 Often reported as one of patients' most problematic symptoms, 87% of people with atopic dermatitis say they are seeking freedom from itch, with speed of itch relief therefore also prioritized by both patients and physicians. 4-7 Nemluvio is the first approved monoclonal antibody that specifically targets IL-31 receptor alpha, inhibiting the signaling of IL-31. 3,8,9 IL-31 is a neuroimmune cytokine that drives itch and is involved in inflammation and skin barrier dysfunction in atopic dermatitis. 8,10 Nemluvio is also the first and only biologic approved for atopic dermatitis as well as prurigo nodularis with four-week dosing intervals from the start of treatment, and the only option to move to eight-week dosing intervals for appropriate patients with atopic dermatitis. 9 'The relentless itch of atopic dermatitis is not just a symptom; it's a constant burden that disrupts sleep, concentration, and the simple joys of life. Nemolizumab has demonstrated its impact on both itch and skin lesions in atopic dermatitis extensively over the years, and these new data, demonstrating its benefit up to two years, add another layer of confidence to that.' PROFESSOR JONATHAN SILVERBERG Expand The ARCADIA long-term extension study was designed to assess the long-term safety and efficacy of Nemluvio in patients with moderate-to-severe atopic dermatitis up to five years and includes more than 1,900 patients who either completed the initial or maintenance period in ARCADIA 1 or 2, a previous phase II/IIIb study, or were newly enrolled adolescent patients. 1 Results to be presented at the RAD Conference will show that Nemluvio is associated with sustained and increased improvements in skin lesions, itch, sleep, and quality of life during prolonged treatment up to two years. 1 At week 104 in evaluable patients, the interim analysis shows that: More than 85% achieved a 75% reduction in the Eczema Area and Severity Index (EASI) 1 Approximately 85% and 70% achieved an at least four-point improvement in itch, and being itch free or nearly itch free, respectively, when assessed using the SCORing Atopic Dermatitis (SCORAD) Visual Analog Scale (VAS) Pruritus score. Improvements in sleep mirrored those in itch 1 Approximately 60% reached clearance or almost-clearance of skin lesions when assessed using the Investigator's Global Assessment (IGA) score 1 Patients' quality of life improved over time, as measured by the Dermatology Life Quality Index (DLQI) 1 Results also reinforce Nemluvio's rapid onset of action on itch and skin at Week 4, with 49% of patients who entered the long-term extension study naïve to Nemluvio achieving a 75% reduction in the EASI, and 69% achieving an at least four-point improvement in itch when assessed using the SCORAD VAS Pruritus score. 1 Nemluvio was well tolerated in the long-term treatment of atopic dermatitis and no new safety signals were identified. 1 Additional data from both the ARCADIA program in atopic dermatitis, as well as from the OLYMPIA open-label extension study in prurigo nodularis will be presented at RAD 2025, reinforcing Nemluvio's rapid impact on key symptoms of atopic dermatitis, and its long-term efficacy in prurigo nodularis. 11,12 Nemluvio was first approved in August 2024 by the United States Food and Drug Administration (U.S. FDA) for the treatment of adults with prurigo nodularis. 9 In December 2024, it was also approved by the U.S. FDA for the treatment of patients 12 years and older with moderate-to-severe atopic dermatitis, in combination with topical corticosteroids and/or calcineurin inhibitors when the disease is not adequately controlled with topical prescription therapies. 9 To date, Nemluvio is approved for both moderate-to-severe atopic dermatitis and prurigo nodularis by multiple regulatory authorities around the world, including the European Commission. Additional regulatory submissions and reviews are ongoing. More details on Galderma's scientific presentations at RAD can be found here. About Nemluvio Nemluvio was initially developed by Chugai Pharmaceutical Co., Ltd. In 2016, Galderma obtained exclusive rights to the development and marketing of nemolizumab worldwide, except in Japan. In Japan, nemolizumab is marketed as Mitchga ® and is approved for the treatment of prurigo nodularis, as well as pruritus associated with atopic dermatitis in pediatric, adolescent, and adult patients. 13,14 About atopic dermatitis Atopic dermatitis is a common, chronic, and flaring inflammatory skin disease, characterized by persistent itch and recurrent skin lesions. 3,15,16 It affects more than 230 million people worldwide. 3 It is the most common inflammatory skin disease, impacting almost four times more people than psoriasis. 17 Important Safety Information Indications: NEMLUVIO ® (nemolizumab-ilto) is a prescription medicine used: to treat adults and children 12 years of age and older with moderate-to-severe eczema (atopic dermatitis or AD) in combination with prescription therapies used on the skin (topical) when the eczema is not well controlled by topical therapies alone. It is not known if NEMLUVIO is safe and effective in children with atopic dermatitis under 12 years of age. to treat adults with prurigo nodularis. It is not known if NEMLUVIO is safe and effective in children with prurigo nodularis under 18 years of age. Do not take NEMLUVIO if you are allergic to nemolizumab-ilto or to any ingredients in NEMLUVIO. Before taking NEMLUVIO, tell your healthcare provider about all of your medical conditions, including if you: are scheduled to receive any vaccination. You should not receive a live vaccine right before or during treatment with NEMLUVIO. are pregnant or plan to become pregnant. It is not known whether NEMLUVIO will harm your unborn baby. are breastfeeding or plan to breastfeed. It is not known whether NEMLUVIO passes into your breast milk and if it can harm your baby. Tell your doctor about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. NEMLUVIO may cause serious side effects, including: allergic reactions (hypersensitivity). Stop using NEMLUVIO and tell your healthcare provider or get emergency help right away if you get any of the following symptoms: Breathing problems or wheezing Swelling of the face, lips, mouth, tongue, or throat Fainting, dizziness, feeling lightheaded Fast pulse Swollen lymph nodes Joint pain Fever Skin rash (red or rough skin) Nausea or vomiting General ill feeling Cramps in your stomach area The most common side effects of NEMLUVIO include: Eczema: headache, joint pain, hives (itchy red rash or wheals), and muscle aches Prurigo Nodularis: headache and skin rashes: atopic dermatitis (a type of eczema), eczema, and eczema nummular (scattered circular patches) These are not all of the possible side effects of NEMLUVIO. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800- FDA-1088. Please see full Prescribing Information including Patient Information. About Galderma Galderma (SIX: GALD) is the pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ – the skin – meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin we are in shapes our lives, we are advancing dermatology for every skin story. For more information: References Silverberg, JI, et al. Nemolizumab long-term safety and efficacy up to 104 weeks in the ARCADIA open-label extension study in adolescents and adults with moderate-to-severe atopic dermatitis. Presented at Revolutionizing Atopic Dermatitis Conference 2025; June 6-7; Nashville, United States. Silverberg J, et al. Nemolizumab with concomitant topical therapy in adolescents and adults with moderate-to-severe atopic dermatitis (ARCADIA 1 & 2): results from two replicate double-blinded, randomised controlled phase 3 trials. Lancet. 2024;404(10451):445-460. doi: 10.1016/S0140-6736(24)01203-0 Langan SM, et al. Atopic dermatitis [published correction appears in Lancet. 2020;396(10253):758]. Lancet. 2020;396(10247):345-360. doi: 10.1016/S0140- 6736(20)31286-1 Silverberg JI, et al. Patient burden and quality of life in atopic dermatitis in US adults: a population-based cross-sectional study. Ann Allergy Asthma Immunol. 2018;121(3):340-347. doi: 10.1016/ Augustin M, et al. Real-World Treatment Patterns and Treatment Benefits among Adult Patients with Atopic Dermatitis: Results from the Atopic Dermatitis Patient Satisfaction and Unmet Need Survey. Acta Derm Venereol. 2022;7:102:adv00830. doi: 10.2340/actadv.v102.3932 Durno N, et al. Biologics and oral systemic treatment preferences in patients and physicians for moderate-to-severe atopic dermatitis: a discrete choice experiment in the United Kingdom and Germany. J Derm Treatment. 2024;35(1). doi: 10.1080/09546634.2024.2417966 Penton H, et al. Assessing Response in Atopic Dermatitis: A Systematic Review of the Psychometric Performance of Measures Used in HTAs and Clinical Trials. Dermatol Ther (Heidelb). 2023;13(11):2549-2571. doi: 10.1007/s13555-023-01038-3 Silverberg JI, et al. Phase 2B randomized study of nemolizumab in adults with moderate-to-severe atopic dermatitis and severe pruritus. J Allergy Clin Immunol. 2020;145(1):173-182. doi: 10.1016/ Nemluvio U.S. Prescribing Information. Available online. Accessed May 2025 Kwatra SG, Misery L, Clibborn C, Steinhoff M. Molecular and cellular mechanisms of itch and pain in atopic dermatitis and implications for novel therapeutics. Clin Transl Immunology. 2022;11(5):e1390. doi: 10.1002/cti2.1390 Silverberg JI, et al. Nemolizumab was associated with rapid and significant improvements in itch and sleep in patients with moderate-to-severe atopic dermatitis: Results from two global phase 3 pivotal studies (ARCADIA 1 and ARCADIA 2). Presented at Revolutionizing Atopic Dermatitis Conference 2025; June 6-7; Nashville, United States. Yosipovitch G, et al. Nemolizumab long-term efficacy and safety up to 52 weeks in the OLYMPIA open-label extension study in patients with prurigo nodularis: An interim analysis. Presented at Revolutionizing Atopic Dermatitis Conference 2025; June 6-7; Nashville, United States. Chugai Pharmaceutical Co., Ltd. Maruho Obtained Regulatory Approval for Mitchga, the first Antibody Targeting IL-31 for Itching Associated with Atopic Dermatitis. Available online. Accessed May 2025 Chugai Pharmaceutical Co., Ltd. Mitchga Approved for Itching in Pediatric Atopic Dermatitis and Prurigo Nodularis, for its Subcutaneous Injection 30mg Vials. Available online. Accessed May 2025 Ständer S. Atopic dermatitis. N Engl J Med. 2021;384(12):1136-1143. doi:10.1056/NEJMra2023911 Yang G, et al. Skin Barrier Abnormalities and Immune Dysfunction in Atopic Dermatitis. Int J Mol Sci. 2020;21(8):2867. doi: Raharja A, et al. Psoriasis: a brief overview. Clin Med (Lond)