logo
Epiminder Announces Publication of Landmark Clinical Trial Confirming Safety and Efficacy of the Minder® System

Epiminder Announces Publication of Landmark Clinical Trial Confirming Safety and Efficacy of the Minder® System

Business Wirea day ago

MELBOURNE, Australia & DALLAS--(BUSINESS WIRE)-- Epiminder, a pioneer in implantable continuous EEG monitoring (iCEM™), today announced the publication of results from its landmark UMPIRE (sUb-scalp Monitoring ePileptic seIzuREs) clinical trial in Epilepsia validating the safety and efficacy of its iCEM. The study, conducted across leading Australian hospitals, demonstrated Minder's ability to capture high-quality EEG data for extended periods that are comparable to current standard of care scalp-based EEG monitors.
The Minder system is a designated Breakthrough Device and has recently been granted clearance for marketing in the United States by the FDA. A world record five-year continuous EEG recording has recently been reported by Epiminder using the system.
'The UMPIRE results exceeded our expectations, proving that continuous EEG monitoring over years—not just days—is not only possible but transformative for epilepsy management,' said Professor Mark Cook, Epiminder's Founder and Chief Medical Officer.
Key Highlights of UMPIRE Clinical Trial:
The Minder system was found to be safe, with no device or procedure related Serious Adverse Events
EEG signal clarity was comparable to standard of care 10-20 scalp-based recordings
Clinically relevant findings were identified in 88% of drug-resistant epilepsy patients, including patients with frequent unreported seizures
Minder's unique bilateral recording capability revealed clinically relevant findings not possible with unilateral recordings in 23% of patients
Commercial Outlook:
Rohan Hoare, Epiminder's CEO, said, 'We are very pleased with the positive impact that Minder can have on the lives of people with epilepsy. Following the FDA authorization in April 2025, Epiminder will initiate a phased U.S. launch in Q3 2025, targeting major epilepsy centers.'
Please visit Epilepsia for open access to the UMPIRE publication.
Follow Epiminder on LinkedIn and explore Epiminder.com for more information.
About Minder
Minder is a minimally invasive device for continuous monitoring of electrographic activity of the brain, providing epilepsy patients and their doctors with detailed data on brain activity over an extended period. Patients can wear the device as they go about their normal daily activities.
Minder's long-term monitoring of patients outside of a controlled clinical environment provides data needed for better understanding and more effective treatment of underlying conditions, including determining the effectiveness of drug therapies and other potential interventions.
About Epiminder
Founded in 2017 by Professor Mark Cook together with the Bionics Institute, St Vincent's Hospital, the University of Melbourne and Cochlear Limited, Epiminder is a medical device and information solutions company focused on developing diagnostic and treatment tools for epilepsy and other seizure disorders where continuous monitoring is required. Epiminder is headquartered in Melbourne, Australia and has offices in the United States.

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

TransCon® hGH Boosts TransCon® CNP Results in Kids with Achondroplasia by Week 26
TransCon® hGH Boosts TransCon® CNP Results in Kids with Achondroplasia by Week 26

Yahoo

time39 minutes ago

  • Yahoo

TransCon® hGH Boosts TransCon® CNP Results in Kids with Achondroplasia by Week 26

Ascendis Pharma A/S (NASDAQ:ASND) is among the 13 Biotech Stocks with Huge Upside Potential. It reported interim Week 26 data from its Phase 2 COACH Trial, confirming that combining TransCon hGH (lonapegsomatropin) with TransCon CNP (navepegritide) raised annualized growth velocity (AGV) and height Z-scores in children with achondroplasia. A close-up view of a hand manipulating a syringe while delivering TransCon CNP into a tumor. A mean AGV of 9.14 cm/year and a +0.53 Z-score rise were attained by treatment-naïve youngsters (N=12). Children (N=9) treated with TransCon CNP in the past achieved an AGV of 8.25 cm/year with a +0.44 Z-score improvement. The majority of side effects were modest, and safety remained consistent with monotherapies. The COACH Trial is the first to assess this combination in kids between the ages of two and eleven. While TransCon CNP is undergoing FDA priority review, TransCon hGH is approved as SKYTROFA® for juvenile growth hormone insufficiency. The treatment focuses on the FGFR3-CNP signaling imbalance that is at the heart of achondroplasia, a disorder that affects more than 250,000 people worldwide. It is anticipated that the results of week 52 and a scheduled Phase 3 trial in Q4 2025 will further clarify efficacy and long-term benefits. The biopharmaceutical business Ascendis Pharma A/S (NASDAQ:ASND) uses its TransCon technology platform to significantly improve patient outcomes. While we acknowledge the potential of ASND as an investment, we believe certain AI stocks offer greater upside potential and carry less downside risk. If you're looking for an extremely undervalued AI stock that also stands to benefit significantly from Trump-era tariffs and the onshoring trend, see our free report on the best short-term AI stock. READ NEXT: 10 High-Growth EV Stocks to Invest In and 13 Best Car Stocks to Buy in 2025. Disclosure. None.

Diversity Gap Persists in Key Trials for Psoriatic Arthritis
Diversity Gap Persists in Key Trials for Psoriatic Arthritis

Medscape

timean hour ago

  • Medscape

Diversity Gap Persists in Key Trials for Psoriatic Arthritis

An analysis of 29 pivotal drug trials for psoriatic arthritis revealed significant racial disparities, with White individuals making up the majority of trial participants, whereas Asian, Black, and other racial groups remained underrepresented. Geographic disparities in participant inclusion were also observed, with trial sites primarily located in North America and Europe. METHODOLOGY: Researchers conducted a descriptive epidemiologic study to assess the gaps in reporting of racial, ethnic, and geographic data of participants enrolled in pivotal US clinical trials of biologic and targeted synthetic disease-modifying antirheumatic drugs for psoriatic arthritis. They collected data on 14,845 participants enrolled in 29 trials with start dates from April 2000 to April 2019, using three primary public sources: Journal publications, the Drugs@FDA database, and Overall, 16 drugs with varying mechanisms were assessed in these trials: Seven trials each of TNF inhibitors and interleukin 17A or 17A/F inhibitors, four trials each of JAK inhibitors and interleukin 23 inhibitors, three trials of phosphodiesterase 4 inhibitors, and two trials each of cytotoxic T-lymphocyte antigen immunoglobulin and interleukin 12/23 inhibitors. TAKEAWAY: Data on race were reported in 93% of trials, with the most frequent reporting in journal publications (86%), although 46% of them reported the proportion of only White participants. Among participants for whom data on race were available, 92% were White, 5% were Asian, 0.6% were Black, 0.3% were American Indian/Alaska Native, and 0.1% were Native Hawaiian/Pacific Islander individuals. Ethnicity was formally reported in only 41% of trials. The reporting of both race and ethnicity improved over time, reaching full coverage (eight of eight trials) on between 2016 and 2020. Among participants for whom data on ethnicity were available, 11% were Hispanic or Latino individuals. Within the US, the highest participation was reported from Texas (24 trials), Florida and Pennsylvania (22 each), California (20), and Alabama (18), with participation in clinical trials strongly correlated with state population size (correlation coefficient, 0.78; P < .0001). Trial sites were primarily located in North America and Europe, with limited representation in Asia, Africa, and Latin America. IN PRACTICE: 'Standardizing and mandating race and ethnicity reporting across data sources is crucial to ensure transparency and equity. Tailored and multifaceted recruitment strategies are essential to increase diversity and ensure the generalizability of trial results, ultimately aiding clinicians to provide the most effective and informed treatment options for all patients,' the authors wrote. SOURCE: This study was led by Mathieu Choufani, MD, Brigham and Women's Hospital, Boston. It was published online on May 19, 2025, in Arthritis Care & Research . LIMITATIONS: This study relied on the US-centric Office of Management and Budget categories for data on race and ethnicity, which may not have represented international populations. Definitions of categories were inconsistent across data sources. Site-level enrollment details were lacking. The analysis was focused solely on pivotal trials for FDA-approved drugs. DISCLOSURES: This study had no specific outside funding source. One author reported receiving consulting fees and grants from various pharmaceutical organizations and being a member of the board of directors for the Spondyloarthritis Research and Treatment Network. Another author reported owning stocks in UCB and Abcuro.

FDA approves label expansion of AbbVie hepatitis C therapy
FDA approves label expansion of AbbVie hepatitis C therapy

Yahoo

timean hour ago

  • Yahoo

FDA approves label expansion of AbbVie hepatitis C therapy

The US Food and Drug Administration (FDA) has approved the label expansion of AbbVie's Mavyret (glecaprevir/pibrentasvir) for treating adults and paediatric patients three years and older with acute or chronic hepatitis C virus (HCV) infection. The extended indication for this oral pangenotypic direct-acting antiviral (DAA) therapy involves those who have the infection without cirrhosis or with compensated cirrhosis. The therapy is the first and only DAA treatment approved for this patient group. HCV is a blood-borne infectious disease that can lead to serious liver complications. The agency's approval is based on data from a Phase III, single-arm, prospective multicentre trial that evaluated the efficacy and safety of an eight-week treatment of the therapy in adults with acute HCV infection. Findings from the trial demonstrated that the therapy is a highly efficacious treatment option. AbbVie research and development executive vice-president and chief scientific officer Roopal Thakkar stated: "Mavyret has treated more than one million patients with HCV, but we recognise that a significant need remains for patients with acute infection. "The label expansion for Mavyret, coupled with the implementation of 'test and treat' models of care, serves as a tool to support the public health community in treating more patients and bringing us closer to achieving the global 2030 elimination goal." Mavyret had also secured a breakthrough therapy designation from the US regulator for acute HCV. This status expedites the development and review of medicines intended to treat serious conditions when preliminary clinical evidence suggests substantial improvement over current therapies. In May 2025, AbbVie signed a partnership and licensing agreement with US-based ADARx Pharmaceuticals, committing $335m upfront to access its small interfering RNA platform. "FDA approves label expansion of AbbVie hepatitis C therapy" was originally created and published by Pharmaceutical Technology, a GlobalData owned brand. The information on this site has been included in good faith for general informational purposes only. It is not intended to amount to advice on which you should rely, and we give no representation, warranty or guarantee, whether express or implied as to its accuracy or completeness. You must obtain professional or specialist advice before taking, or refraining from, any action on the basis of the content on our site. Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store