
Results from the VirTus Respiratory Research Ltd Human Rhinovirus Challenge Model Used to Advance Altesa BioSciences' Lead Medicine into Advanced Clinical Trials
LONDON--(BUSINESS WIRE)--VirTus Respiratory Research Ltd, a leading respiratory-focused contract research organisation (CRO), today announced that results from their human rhinovirus challenge model in patients with chronic obstructive pulmonary disease (COPD) provided Altesa BioSciences with compelling evidence to advance their lead drug candidate, vapendavir, into large scale, late-stage clinical trials.
"These positive results underline the effectiveness of our human virus challenge model to rapidly assess clinical efficacy of novel medicines early in their clinical development pathway," said Professor Sebastian Johnston, Co-founder and CMO at Virtus.
Rhinovirus infection is the cause of at least half of the acute respiratory deteriorations experienced by the millions of patients with chronic obstructive lung disease. 'Before advancing vapendavir into clinical trials testing vapendavir on thousands of patients costing tens of millions of dollars, it was critical to demonstrate beneficial effects of the drug in a proof-of-concept study," said Dr. Brett Giroir, CEO of Altesa and former US Assistant Secretary for Health and Acting FDA Commissioner. 'After literally searching the globe, we determined that VirTus was the only place that could safely, effectively, and reliably conduct this study on actual volunteers with COPD.'
The randomised, placebo-controlled study enrolled and evaluated 40 volunteers with COPD, the 3 rd leading cause of death worldwide. Pre-screened COPD patients were challenged with a known-to-be safe strain of rhinovirus and randomized after onset of symptoms. Recruitment involved contacting over 10,000 potential volunteers primarily through targeted social media campaigns, highlighting the innovative approach VirTus employs to ensure efficient and successful participant engagement.
"These positive results underline the effectiveness of our human virus challenge model to rapidly assess clinical efficacy of novel medicines early in their clinical development pathway," said Professor Sebastian Johnston, Co-founder and Chief Medical Officer (CMO) at VirTus. "This approach allows our biotech and pharmaceutical industry partners to gain early, meaningful clinical data, helping them to make confident go/no-go decisions in their drug development pipeline."
VirTus' human virus challenge model offers sponsors the opportunity to evaluate treatments in a controlled environment, significantly reducing uncertainty, time and cost associated with much larger, traditional early clinical development studies.
'By leveraging the wealth of experience of Professor Johnston and the VirTus team, we have learned how to best deploy vapendavir so that is has the best chance of improving the lives of people with COPD – which is our ultimate goal and one that I have dedicated my career to achieving,' said Dr. Kate Knobil, CMO at Altesa and former CMO of GSK.
Dr Michael Edwards, Co-founder and Managing Director at VirTus, added, "We're delighted to support Altesa BioSciences in achieving these encouraging results with vapendavir. This successful collaboration showcases the strength and reliability of our human challenge studies, reinforcing our mission to accelerate innovative treatments for respiratory illnesses worldwide."
About VirTus Respiratory Research Ltd
VirTus Respiratory Research Ltd is a CRO co-led by Professor Sebastian Johnston and Dr. Michael Edwards, both of Imperial College London, United Kingdom. VirTus is dedicated to accelerating the development of novel therapies for the treatment and prevention of respiratory virus infections, which are the leading cause of acute attacks (exacerbations) in chronic respiratory diseases such as asthma, COPD and bronchiectasis. VirTus conducts both pre-clinical and early-phase clinical studies, specialising in human virus challenge models to generate high-quality data that supports the advancement of new therapeutics into later-stage development.
The rhinovirus challenge model
At VirTus Respiratory Research Ltd, the rhinovirus challenge model is used to generate early signals of clinical efficacy in a tightly controlled, reproducible setting. By exposing volunteers to rhinovirus infection under monitored conditions, the model provides detailed assessment of how a treatment impacts symptoms, virus load and immune/inflammatory responses. For our partners, this model acts as a critical go/no-go decision maker ahead of much larger, costlier Phase 2b/3 trials. It helps answer key questions early, including clinical efficacy, dose selection and endpoint optimisation. Sponsors benefit from accelerated timelines, early go/no-go insights, de-risking development programs by identifying promising candidates, or ruling out ineffective ones, at an earlier stage, ultimately optimising resource allocation and increasing the likelihood of downstream success.
About Vapendavir
Vapendavir, taken orally in pill form, is a clinical-stage antiviral medicine with potent activity against 97% of rhinoviruses tested and other respiratory enteroviruses. It prevents the virus from entering human cells as well as preventing it from reproducing. Vapendavir is currently in advanced clinical trials for the treatment of rhinovirus infections in people living with COPD. Vapendavir has a similar mechanism of action to the FDA approved HIV capsid inhibitor, lenacapavir marketed by Gilead Sciences.
About COPD
COPD is a life-limiting chronic lung condition that affects hundreds of millions of people worldwide. COPD is now the third leading cause of death globally, with prevalence continuing to rise due to aging populations and ongoing exposure to risk factors such as smoking and air pollution. COPD imposes a huge burden on individuals and healthcare systems alike, with high morbidity due to progressive lung function decline and frequent exacerbations, alongside enormous ($49 billion in the US) healthcare costs associated with long-term treatment and prolonged and frequent hospital admissions.
About Altesa
Altesa BioSciences is a clinical-stage pharmaceutical company dedicated to developing new treatments for age-old threats to human health: high-consequence viral infections. These infections are particularly severe in vulnerable people, including those with chronic health conditions, like lung diseases, as well as the elderly and many people in underserved communities.

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Yahoo
12 hours ago
- Yahoo
Neurogene Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
NEW YORK, June 06, 2025--(BUSINESS WIRE)--Neurogene Inc. (Nasdaq: NGNE), a clinical-stage company founded to bring life-changing genetic medicines to patients and families affected by rare neurological diseases, today announced that the Compensation Committee of the Company's Board of Directors approved the grant of non-qualified stock options to purchase an aggregate of 39,345 shares of the Company's common stock to four new employees (the "Inducement Grants") on June 5, 2025 (the "Grant Date"). The Inducement Grants have been granted pursuant to the Company's 2025 Inducement Plan (the "Plan"). The Inducement Grants were granted as an inducement material to these individuals entering into employment with Neurogene in accordance with Nasdaq Listing Rule 5635(c)(4). The Inducement Grants have an exercise price per share that is equal to the closing price of Neurogene's common stock on the Grant Date. The Inducement Grants will vest over four years, with 25 percent vesting on the first anniversary of the vesting commencement date and thereafter in equal portions upon the lapse of each three-month period over the following 36-month period, subject to the employee's continued employment with Neurogene through the applicable vesting dates. About Neurogene The mission of Neurogene is to treat devastating neurological diseases to improve the lives of patients and families impacted by these rare diseases. Neurogene is developing novel approaches and treatments to address the limitations of conventional gene therapy in central nervous system disorders. This includes selecting a delivery approach to maximize distribution to target tissues and designing products to maximize potency and purity for an optimized efficacy and safety profile. The Company's novel and proprietary EXACT™ transgene regulation platform technology allows for the delivery of therapeutic levels while limiting transgene toxicity associated with conventional gene therapy. Neurogene has constructed a state-of-the-art gene therapy manufacturing facility in Houston, Texas. CGMP production of NGN-401 was conducted in this facility and will support pivotal clinical development activities. For more information, visit View source version on Contacts Company Contact: Cara MayfieldVice President, Corporate Investor Contact: Melissa ForstArgot PartnersNeurogene@ 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
Yahoo
13 hours ago
- Yahoo
Neurogene Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
NEW YORK, June 06, 2025--(BUSINESS WIRE)--Neurogene Inc. (Nasdaq: NGNE), a clinical-stage company founded to bring life-changing genetic medicines to patients and families affected by rare neurological diseases, today announced that the Compensation Committee of the Company's Board of Directors approved the grant of non-qualified stock options to purchase an aggregate of 39,345 shares of the Company's common stock to four new employees (the "Inducement Grants") on June 5, 2025 (the "Grant Date"). The Inducement Grants have been granted pursuant to the Company's 2025 Inducement Plan (the "Plan"). The Inducement Grants were granted as an inducement material to these individuals entering into employment with Neurogene in accordance with Nasdaq Listing Rule 5635(c)(4). The Inducement Grants have an exercise price per share that is equal to the closing price of Neurogene's common stock on the Grant Date. The Inducement Grants will vest over four years, with 25 percent vesting on the first anniversary of the vesting commencement date and thereafter in equal portions upon the lapse of each three-month period over the following 36-month period, subject to the employee's continued employment with Neurogene through the applicable vesting dates. About Neurogene The mission of Neurogene is to treat devastating neurological diseases to improve the lives of patients and families impacted by these rare diseases. Neurogene is developing novel approaches and treatments to address the limitations of conventional gene therapy in central nervous system disorders. This includes selecting a delivery approach to maximize distribution to target tissues and designing products to maximize potency and purity for an optimized efficacy and safety profile. The Company's novel and proprietary EXACT™ transgene regulation platform technology allows for the delivery of therapeutic levels while limiting transgene toxicity associated with conventional gene therapy. Neurogene has constructed a state-of-the-art gene therapy manufacturing facility in Houston, Texas. CGMP production of NGN-401 was conducted in this facility and will support pivotal clinical development activities. For more information, visit View source version on Contacts Company Contact: Cara MayfieldVice President, Corporate Investor Contact: Melissa ForstArgot PartnersNeurogene@
Yahoo
13 hours ago
- Yahoo
Wildfire smoke has caused air quality in southern Ontario and Quebec to plummet — 8 best AHAM-certified air purifiers
As wildfires continue to rage throughout Western Canada, thousands of residents of Manitoba, Alberta and Saskatchewan have been evacuated, and millions in the surrounding areas face hazardous air quality conditions. Manitoba, the epicentre of the wildfires, remains under a province-wide state of emergency as extreme fire conditions force thousands to flee. Premier Wab Kinew has called it Manitoba's "largest evacuation" in living memory. More than 17,000 Manitobans have been evacuated, along with over 4,000 people in Alberta and between 10,000 and 15,000 residents in Saskatchewan. Saskatchewan Premier Scott Moe declared a province-wide state of emergency on May 29, one day after his Manitoba counterpart, Kinew, did the same. Smoke from the Canadian wildfires has triggered air quality warnings in several provinces and surrounding U.S. states. As of Friday, June 6, much of southern Ontario and southern Quebec, including Toronto, Ottawa and Montréal, have been placed under special air quality alerts. As of 12:43 p.m. EST on Friday., IQAir, a Swiss technology company, ranked Toronto as the city with the second-worst air quality in the world and Montréal as the third-worst. On days with poor air quality, people are more likely to experience shortness of breath, difficulty breathing and coughing or wheezing — especially if they have a chronic respiratory disease like asthma or chronic obstructive pulmonary disease (COPD). The small particles in wildfire smoke can get into your eyes and bloodstream, and if you have a heart or lung problem, you may experience problems earlier and at lower smoke levels. According to Health Canada, using a portable air purifier that can filter fine particles is one way to protect your indoor environment from smoke pollution. Air purifiers, also known as air cleaners, can improve indoor air quality by removing small contaminants that can harm your health. According to the health authority, you should prioritize the following when choosing an air purifier: Look for a device certified by the Association of Home Appliance Manufacturers (AHAM). Choose an air purifier sized appropriately for the room you want to put it in. Consider the clean air delivery rate (CADR) for the room size. The CADR describes how well the device reduces tobacco smoke, dust, pollen and wildfire smoke. To reduce fine particles, select a device with the highest CADR. Choose an air purifier with a high-efficiency particulate air (HEPA) filter. Avoid devices that produce ozone. Not all air purifiers are made equal. Following Health Canada's recommendations, we've listed eight AHAM-certified air purifiers and included information about recommended room sizes and CADR ratings. Room Size: 47 ft2 Tobacco Smoke CADR: 30 Dust CADR: 41 PM2.5 CADR: 35 Pollen CADR: 52 Volts / Frequency: 120V / 60Hz Room Size: 201 ft2 Tobacco Smoke CADR: 112 Dust CADR: 112 Pollen CADR: 112 Volts / Frequency: 100V / 50Hz | 240V / 60Hz Room Size: 140 ft2 Tobacco Smoke CADR: 90 Dust CADR: 101 PM2.5 CADR: 95 Pollen CADR: 119 Volts / Frequency: 120V / 60Hz Room Size: 170 ft2 Tobacco Smoke CADR: 110 Dust CADR: 120 Pollen CADR: 130 Volts / Frequency: 120V / 60Hz Room Size: 206 ft2 Tobacco Smoke CADR: 133 Dust CADR: 141 Pollen CADR: 145 Volts / Frequency: 120V / 60Hz Room Size: 200 ft2 Tobacco Smoke CADR: 132 Dust CADR: 130 Pollen CADR: 152 Volts / Frequency: 120V / 60Hz Room Size: 250 ft2 Tobacco Smoke CADR: 161 Dust CADR: 160 Pollen CADR: 170 Volts / Frequency: 120V / 60Hz Room Size: 358 ft2 Tobacco Smoke CADR: 231 Dust CADR: 240 PM2.5 CADR: 236 Pollen CADR: 259 Volts / Frequency: 120V / 60Hz