Phase 2b/3 Alzheimer’s trial enrolment expected to reach 100 this quarter, triggering an interim analysis 6 months laterSYDNEY, April 30, 2025 (GLOBE NEWSWIRE) -- Actinogen Medical Limited (ASX: ACW) announces that its Alzheimer’s disease phase 2b/3 trial has now enrolled 60 participants and expects to reach 100 by the end of this quarter. That milestone will trigger an interim analysis of available trial data by an independent Data Monitoring Committee approximately 6 months later. Final results for the fu ...

Core Insights - Silo Pharma, Inc. has filed a patent application for its neurology drug SPC-14, aimed at treating Alzheimer's disease, which is exclusively licensed from Columbia University [1][3] Patent Details - The patent titled "Compositions and Methods for the Treatment of Alzheimer's Disease and Other Neurogenerative Disease" focuses on SPC-14's mechanism of action, targeting glutamate receptor NDMAR and serotonin 5-HT4 to alleviate cognitive and neuropsychiatric symptoms in Alzheimer's disease [2][4] Drug Development - Early pre-clinical studies indicate that SPC-14 has the potential to improve cognitive memory function [3] - The drug has shown efficacy in preclinical studies against luteinizing hormone (LH) stress, reducing learned helplessness, perseverative behavior, and hyponeophagia, which is a measure of anxiety [4] Company Overview - Silo Pharma is a developmental stage biopharmaceutical company that focuses on addressing underserved conditions, including stress-induced psychiatric disorders, chronic pain, and central nervous system diseases [5] - The company's portfolio includes other innovative programs such as SPC-15 for PTSD and SP-26 for fibromyalgia and chronic pain, alongside preclinical assets targeting Alzheimer's disease and multiple sclerosis [5]

Core Viewpoint - The Davos Alzheimer's Collaborative (DAC) is launching the North African Dementia Registry (NADR) project in collaboration with PacBio, The American University in Cairo (AUC), and UCL to enhance understanding of Alzheimer's disease and dementia in diverse populations, particularly in North Africa [1][2][3] Group 1: Project Overview - The NADR is the first dementia-focused registry in North Africa, aiming to collect biosamples, conduct cognitive assessments, and perform digital phenotyping [2] - The initiative will create a comprehensive multi-omics dataset to explore genetic and environmental factors related to Alzheimer's disease [2][3] - Data generated will be accessible via the Alzheimer's Disease Data Initiative (ADDI) platform, promoting global research collaboration [3] Group 2: Technological Partnership - PacBio will provide its advanced long-read sequencing technology to generate high-quality genomic data essential for understanding the genetic landscape of Alzheimer's disease [2][3] - The collaboration aims to identify new diagnostic tools and therapeutic solutions for Alzheimer's disease [3] Group 3: Importance of Diversity in Research - The project addresses the underrepresentation of North African populations in dementia research, which is crucial given the region's genetic diversity [2][3] - Insights gained from this research are expected to inform locally relevant prevention and intervention strategies [3] Group 4: Broader Implications - DAC aims to extend global research efforts beyond traditional Western populations to include diverse populations in the Global South, where most Alzheimer's patients reside [4] - The initiative aligns with DAC's goal to implement health system solutions that are globally applicable and to promote brain health throughout the lifespan [4][5]

Core Insights - The Davos Alzheimer's Collaborative (DAC) has partnered with PacBio to support the North African Dementia Registry (NADR) project, aiming to enhance understanding of Alzheimer's disease in North African populations [1][2][3] - This initiative is the first dementia-focused registry in North Africa, addressing the underrepresentation of these populations in dementia research [2][3] - The collaboration will utilize PacBio's long-read sequencing technology to create a comprehensive multi-omics dataset, facilitating research into genetic and environmental factors related to Alzheimer's disease [2][3] Company Insights - PacBio is recognized for its advanced sequencing solutions, which are crucial for generating high-quality genomic data necessary for understanding the complex genetic landscape of Alzheimer's disease [3][12] - The partnership aligns with PacBio's commitment to enabling genomic discoveries that improve human health globally [3][12] - The data generated from this collaboration will be accessible through the Alzheimer's Disease Data Initiative (ADDI) platform, promoting further research and innovation in Alzheimer's disease [3][4] Industry Insights - The DAC initiative aims to extend global research efforts beyond traditional Western populations to include diverse populations in the Global South, where a significant number of Alzheimer's cases exist [4] - By 2050, it is projected that over 150 million families and half a billion people will be affected by dementia, highlighting the urgent need for effective research and intervention strategies [4] - The NADR project will enable the collection of biosamples, cognitive assessments, and digital phenotyping, which are essential for developing locally relevant prevention and intervention strategies [2][3]

NEW YORK, April 21, 2025 (GLOBE NEWSWIRE) -- Anavex Life Sciences Corp. (“Anavex” or the “Company”) (Nasdaq: AVXL), a clinical-stage biopharmaceutical company focused on developing innovative treatments for Alzheimer's disease, Parkinson's disease, schizophrenia, neurodevelopmental, neurodegenerative, and rare diseases, including Rett syndrome, and other central nervous system (CNS) disorders, today announced that Marwan Noel Sabbagh, MD, Professor of Neurology at Barrow Neurological Institute and Chairman ...

Core Insights - Lecanemab has received Marketing Authorization in the EU, marking it as the first therapy targeting the underlying cause of Alzheimer's disease to be approved in this region [1][2] - The treatment is specifically indicated for adult patients with mild cognitive impairment and mild dementia due to Alzheimer's disease who are ApoE ε4 non-carriers or heterozygotes with confirmed amyloid pathology [1][2] - The approval applies to all 27 EU Member States, as well as Iceland, Liechtenstein, and Norway [1][3] Company Overview - Eisai Co., Ltd. and Biogen Inc. are collaborating on the development and commercialization of lecanemab, with Eisai leading the global development and regulatory submissions [2][8] - The approval of lecanemab in the EU is the thirteenth approval globally, following its benefits to thousands of patients in the U.S., Japan, and other regions [2][6] - Eisai aims to work with national reimbursement authorities and healthcare providers to ensure access to lecanemab for eligible patients as soon as possible [2] Clinical Data - The authorization was based on Phase 3 data from the Clarity AD clinical trial, which involved 1,795 patients with early Alzheimer's disease [4][6] - In the trial, lecanemab reduced clinical decline on the CDR-SB scale by 31% at 18 months compared to placebo [4][6] - The secondary endpoint showed a 33% less decline in daily living activities for patients treated with lecanemab compared to placebo [4][6] Market Context - Alzheimer's disease currently affects an estimated 15.2 million people with mild cognitive impairment and 6.9 million with mild dementia in Europe, indicating a significant unmet need for effective treatments [1][6] - Lecanemab is the only approved Aβ monoclonal antibody that preferentially binds and clears toxic protofibrils, which are key contributors to neuronal injury in Alzheimer's disease [1][4] - The approval of lecanemab represents a landmark advancement in a field that has seen little innovation over the past two decades [2][6]

Core Insights - The Ad Council and Alzheimer's Association launched new PSAs to raise awareness of early signs of Alzheimer's, particularly targeting Black Americans who are at a higher risk of developing the disease [1][2] - The campaign aims to encourage families to discuss potential signs of Alzheimer's earlier, as early detection is crucial for effective care and management [2][5] Campaign Details - The PSAs are part of the "Some Things Come with Age" campaign and focus on educating pre-care partners about the differences between normal aging and early signs of Alzheimer's [1][4] - Recent data indicates that 19% of Black Americans aged 65 and older are diagnosed with Alzheimer's, compared to 10% of white Americans, highlighting the need for targeted outreach [2][5] - The campaign includes resources available at 10signs.org, which provides information on early warning signs and tips for initiating conversations about cognitive health [7] Creative Approach - The creative content emphasizes familial love and the importance of recognizing subtle cognitive changes that may indicate Alzheimer's, such as difficulty completing familiar tasks [4][6] - A three-minute long-form video is included to further illustrate the relational bonds and the role of pre-care partners in recognizing early signs [4] Media and Outreach - The PSAs will be distributed nationally through donated media, with support from various platforms including LatiNation, Meta, and SiriusXM Media [6] - Research from the Ad Council shows that individuals aware of the campaign are three times more likely to understand the difference between aging signs and Alzheimer's signs [5] Background Information - The Alzheimer's Association is dedicated to Alzheimer's care, support, and research, aiming to accelerate global research and improve early detection and quality care [8] - The Ad Council has a long history of creating impactful social campaigns and collaborates with various organizations to address pressing health issues [9]

Core Insights - Roche Holdings AG presented new data on trontinemab at the AD/PD 2025 International Conference, highlighting its potential in Alzheimer's disease treatment and the Elecsys pTau181 plasma test's ability to rule out amyloid pathology [1][4]. Group 1: Trontinemab Study Results - The ongoing Phase 1b/2a Brainshuttle AD study of trontinemab showed dose-dependent rapid amyloid depletion from the brain [1]. - Preliminary results indicated that trontinemab reduced amyloid levels below the 24 centiloid threshold in 81% of participants (21 out of 26) in the 3.6 mg/kg dose group after 28 weeks [6]. - The study reported a favorable safety profile, with amyloid-related imaging abnormalities (ARIA-E) observed in less than 5% of participants, and only one case associated with mild symptoms [3]. Group 2: Elecsys pTau181 Plasma Test - Results from a multicenter study involving 604 participants demonstrated the Elecsys pTau181 plasma test's potential to accurately rule out amyloid pathology in individuals with cognitive impairment [4]. - Roche anticipates that the Elecsys pTau181 test will be available in Europe by late 2025, followed by the U.S. [4]. Group 3: Future Developments - Roche plans to initiate a Phase 3 program for trontinemab later this year [4]. - The company continues to reinforce its commitment to advancing research in Alzheimer's disease through ongoing studies and new testing methods [4]. Group 4: Market Reaction - Following the presentation of the new data, Roche's stock (RHHBY) closed lower by 4.37% to $37.65 [5].

Acumen Pharmaceuticals, Inc. (NASDAQ:ABOS) Q4 2024 Earnings Conference Call March 27, 2025 8:00 AM ET Company Participants Alex Braun - Head, Investor Relations Dan O???Connell - Chief Executive Officer Matt Zuga - Chief Financial Officer and Chief Business Officer Jim Doherty - President and Chief Development Officer Eric Siemers - Chief Medical Officer Conference Call Participants Jason Zemansky - Bank of America Pete Stavropoulos - Cantor Fitzgerald Ting Liu - UBS Tom Shrader - BTIG Ananda Ghosh - H. C. ...

InMed Pharmaceuticals (INM) Update / Briefing November 12, 2024 02:00 PM ET Speaker0 Hello, everyone. Thank you for attending today's Fierce Biotech webinar, Alzheimer's Outlook, The Next Step. I understand we have a great number of attendees on today's webinar, and I want to thank InMed Pharmaceuticals for sponsoring this presentation. My name is Phyllis Fearle, and I will be moderating today's conversation. But before we get started, here's a few quick housekeeping notes. You can access closed captions fr ...