Albus Health Device Detects Early Warning Signs of Child Asthma Attacks Up To Five Days Before Onset

Albus Health Device Detects Early Warning Signs of Child Asthma Attacks Up To Five Days Before Onset

Research presented at British Thoracic Society Winter Meeting demonstrates potential for revolutionary shift in respiratory care

Technology set to transform respiratory clinical trials: single device delivers continuous endpoint data across multiple parameters with minimal patient burden

OXFORD, UK; November 29, 2024 — Albus Health, the healthcare technology company pioneering monitoring of nocturnal health parameters including cough and breathing patterns, announces results from a clinical study at the British Thoracic Society Winter Meeting 2024 this week. The data revealed that Albus Home, the company’s AI-powered, innovative non-contact monitoring device with advanced algorithms, can detect warning signs of asthma attacks in children up to five days before they occur, potentially transforming how respiratory conditions are managed globally.

The groundbreaking study, conducted at Birmingham Children’s Hospital and Royal Brompton Hospital, demonstrated that the Albus Home device successfully identified significant changes in children’s respiratory health days before they required emergency steroid treatment for asthma attacks. This early warning window could provide crucial time for medical intervention, potentially preventing emergency hospitalisations and improving patient outcomes.

“For the first time, we have technology that can reliably monitor children while they sleep, without any disruption to their normal routine,” said Dr. Prasad Nagakumar, Director for Research at Birmingham Children’s Hospital and lead researcher on the study. “The device’s ability to detect changes up to five days before an attack represents a potential paradigm shift in asthma management, offering a window of opportunity for early intervention that simply hasn’t existed before.”

Night-time symptoms are crucial early warning signs of respiratory disease deterioration, yet until now, healthcare providers have remained blind to at-home symptoms while patients and carers often identify deterioration too late. The Childhood Home Asthma Monitoring Project (CHAMP) study recruited 100 children with asthma. The researchers analysed 47 asthma attacks across 28 children, finding that nocturnal cough frequency and respiratory rate began increasing five days before attacks occurred. In earlier studies, the device achieved clinical-grade accuracy, with 98.3% accuracy in respiratory rate measurement and 99% correlation in cough detection against gold standards.

Following insights from the study and feedback from participants and carers, Albus has developed a next-generation device that also measures heart rate, sleep parameters and air quality metrics. The device’s unique set of sensors, along with Bluetooth, Wi-Fi, and cellular connectivity, unlocks unprecedented opportunities in remote patient monitoring.

“This study validates our mission to revolutionise respiratory care through passive monitoring and early detection,” said Mikesh Udani, CEO of Albus Health. “Our technology has the potential to transform both patient care and clinical trials for several chronic diseases. By providing objective, continuous monitoring data, we can help pharmaceutical companies demonstrate response to treatment more efficiently while generating valuable insights for future drug development.”

The ability to detect and measure these subtle respiratory changes with such precision represents a major advance for both patient care and drug development. While current clinical trials rely heavily on subjective symptom reporting and limited spot-checks of respiratory function, the Albus Home device provides continuous, real-world data throughout the night – exactly when respiratory symptoms typically worsen. This has significant implications for respiratory drug development, where poor quality data collection and unreliable symptom reporting often necessitate larger, longer, and more expensive clinical trials. The Albus Home device offers pharmaceutical companies the ability to capture objective respiratory and sleep endpoints continuously, which can be used to bring new classes of therapies to asthma patients, monitor patient outcomes for post approval studies, and expand indications and labels for existing drugs.

Albus Home has already been deployed commercially to collect real world evidence on treatment response in a US-based Phase IV trial by a major pharmaceutical company. Albus is in advanced negotiations with several additional partners, highlighting strong industry confidence in the technology’s potential to transform both patient care and clinical research. Albus is now focused on expanding its clinical evidence base and set of parameters monitored, while scaling its platform to address the growing global burden of respiratory disease.

For more information about Albus Health and its unique respiratory monitoring technology, visit www.albushealth.com.

This study was funded through The Artificial Intelligence in Health and Care Award, one of the NHS AI Lab programmes. The competitive award scheme is run by DHSC. The AI Award has made funding available to accelerate the testing and evaluation of artificial intelligence technologies which meet the aims set out in the NHS Long Term Plan. In addition to Birmingham Women’s and Children’s Hospital and the Royal Brompton Hospital, partners include Imperial College London, Asthma + Lung UK, and Health Innovation Oxford.

About Albus Health

Albus Health, a spin-off from the University of Oxford, is pioneering nocturnal respiratory insights through its advanced non-contact monitoring system. The company has developed a revolutionary technology that addresses significant unmet needs in both clinical trials and respiratory care, where the inability to reliably monitor patients whilst they are in bed leads to missed early warnings of severe attacks and compromised clinical development data. The company’s bedside device combines proprietary hardware with advanced AI algorithms to deliver automated, clinical-grade insights with unprecedented accuracy in real-world settings. With its first pharmaceutical contract secured and multiple trials underway at leading institutions, Albus Health is positioned to transform respiratory care from reactive to predictive, while significantly enhancing the efficiency of global respiratory clinical trials. The company’s initial focus on respiratory conditions provides a clear path to commercial success, with potential for expansion into other chronic conditions through its established hardware and software platforms.

For Media enquires:

Sukaina Virji, Kate Hall

Albus@icrhealthcare.com

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ENA Respiratory Receives USPTO Notice of Allowance for Key Patent Covering INNA-051, a First-in-Class Antiviral Innate Immunomodulator

MELBOURNE, Australia, May 08, 2024 (GLOBE NEWSWIRE) — ENA Respiratory, a clinical-stage pharmaceutical company developing innate immune modulators for the prevention of complications associated with respiratory viral infections in at-risk populations, announces today that it has received a Notice of Allowance from the U.S. Patent and Trademark Office (USPTO) for patent application US 18/112091 entitled “Novel molecules” covering claims for its lead program, INNA-051 and its composition.

A virus-agnostic intranasal antiviral host defence immunomodulator, INNA-051 is a potent first-in-class agonist of toll-like receptor 2/6 (TLR2/6) which plays a key role in recognizing pathogens and triggering the innate immune response.

This USPTO allowance further strengthens ENA Respiratory’s strong IP portfolio related to INNA-051, with 30 granted patents and allowed applications in the major markets, including the US, Europe, the United Kingdom, Japan and China. The portfolio covers seven distinct patent families, with claims directed to the composition of matter for INNA-051 and various backup molecules, formulations and method of use protection, as part of a comprehensive lifecycle management strategy. ENA Respiratory has an additional 39 pending applications in various jurisdictions.

ENA Respiratory’s CEO, Christophe Demaison, PhD said: “Our IP portfolio provides robust and long-lasting protection with potential exclusivity for INNA-051 out to at least 2042 and likely for five years post that date. This gives us great confidence in the future global commercial value of our innate immune modulators as we continue to drive forwards in clinical development.”

Having demonstrated accelerated viral clearance and local stimulation of antiviral host defences for INNA-051 in a Phase IIa proof-of-principle study using a liquid formulation in an influenza-challenge model, ENA Respiratory has developed an improved dry powder formulation to take into further clinical development. This formulation recently received FDA IND clearance and the Company has submitted ethics approval for a Phase 1b study in Australia. This study is expected to be initiated in mid-2024 with the aim to assess the safety, tolerability, pharmacodynamics, and pharmacokinetics of the dry powder formulation of INNA-051 in older adults.

About ENA Respiratory

ENA Respiratory is a clinical-stage pharmaceutical company tackling serious respiratory viral infections through the development of host defence immune modulators which locally prime and boost the body’s innate immune response – the natural first line of defence. Being virus-agnostic, immune modulators are complementary to often virus-specific vaccines and existing direct-acting antivirals.

The company’s lead product, INNA-051, is a potent agonist of toll-like receptor 2/6 (TLR2/6) which plays a key role in recognising pathogens and triggering the innate immune response. With a safe profile supporting prophylaxis use, it has demonstrated accelerated viral clearance and stimulation of antiviral host defences, including IFN Type I & III responses, in a Phase IIa proof-of-principle study using an influenza-challenge model. INNA-051 is being developed as a convenient, once-a-week nasal dry powder product to prevent complications associated with respiratory viral infections in at-risk populations, including the elderly, those with an underlying medical condition (including chronic lung conditions, diabetes, kidney disease, and cardiovascular disease) and individuals with occupational risk (e.g. first responders, military or essential services personnel).

Headquartered in Melbourne, Australia, the company has raised US$26M (AU$44million) in equity financing from Brandon Capital, The Minderoo Foundation and Uniseed. It is partnered with the COPD Foundation to support the clinical development of INNA-051 in COPD and has been awarded a US$8.18million contract from the U.S. Department of Defence. It is a member BLUE KNIGHT™, a joint initiative between Johnson & Johnson Innovation and BARDA designed to accelerate next-gen potential solutions for future pandemics.

For more information, please visit https://enarespiratory.com

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Biophytis – therapeutics to slow down the degenerative processes associated with aging

Biophytis is a clinical-stage biotechnology company specialized in the development of therapeutics that are aimed at slowing the degenerative processes associated with aging and improving functional outcomes for patients suffering from age-related diseases, including severe respiratoy failure in patients suffering from COVID-19.

Biophytis - therapeutics to slow down the degenerative processes associated with aging

Biophytis SA, founded in 2006, develops drug candidates targeting diseases of aging. Using its technology and know-how, Biophytis has begun clinical development of innovative therapeutics to restore the muscular and visual functions in diseases with significant unmet medical needs. Specifically, the company is advancing two proprietary drug candidates into mid-stage clinical testing this year: Sarconeos (BIO101) to treat sarcopenic obesity and Macuneos (BIO201) to treat dry age-related macular degeneration (AMD). The business model of BIOPHYTIS is to ensure the conduct of the project until clinical activity in the patient is proven, then to license the technologies in order to continue the development in partnership with a pharmaceutical laboratory. The company was founded in partnership with researchers at the UPMC (Pierre and Marie Curie University) and collaborates with scientists at the Institute of Myology, and the Vision Institute

Its lead drug candidate, Sarconeos (BIO101), is an orally administered small molecule in development for the treatment of neuromuscular diseases, including sarcopenia and Duchenne muscular dystrophy (DMD). Our second drug candidate, Macuneos (BIO201), is an orally administered small molecule in development for the treatment of retinal diseases, including dry AMD and Stargardt disease.

Biophytis also has preclinical efficacy data for Sarconeos (BIO101) in Spinal Muscular Atrophy (SMA), a rare neuromuscular disease. Spinal Muscular Atrophy is a rare progressive neurodegenerative disease that robs an individual of the ability to walk, eat and breathe. SMA is the leading genetic cause of death in infants. Symptoms may appear in the first 6 months of life (type 1, the most severe and common), in infancy (types 2 and 3) or in adulthood (type 4, the least common form). SMA affects 1 in 11,000 births in the United States each year, and about 1 in 50 Americans is a genetic carrier.

More info : www.biophytis.com

Keywords for Biophytis :

neuromuscular diseases, dry age-related macular degeneration, AMD, ophthalmology, infectious diseases, COVID19, Asthma, COPD, small molecule, sarcopenia, Stargardt disease, Duchenne muscular dystrophy , DMD, preclinical stage pharma company, clinical stage pharma company , Spinal Muscular Atrophy , rare diseases , aging

Celon Pharma had the largest IPO on the Polish capital market in 2016

Celon Pharma

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