Posted: 29 January 2024
Starpharma today announces the results of the post-market[2] clinical study of Viraleze™ nasal spray in participants with COVID-19, demonstrating that Viraleze™ reduced SARS-CoV-2 viral load in the nose, increased the rate of virus clearance from the nose, improved key symptoms of COVID-19, including loss of smell (anosmia), and was well-tolerated.
The post-market, double-blind, placebo-controlled clinical study enrolled a total of 222 participants eligible for safety analyses, with 197 of these participants having laboratory-confirmed SARS-CoV-2 infection and eligible for efficacy analyses. Participants were randomised in a 1:1 ratio and self-administered Viraleze™ or a placebo nasal spray four times daily for seven days.
The results from this study provide significant clinical evidence of the performance of Viraleze™ in humans that will support regulatory processes for the transition to the new European Medical Device Regulations (MDR), which will come into full effect in 2029. The positive data will also support ongoing marketing and commercial activities for the product.
SARS-CoV-2 Viral Load
Viraleze™ achieved a statistically significantly lower level of SARS-CoV-2 viral load[3] in the nose over the 7-day treatment period, which was the primary endpoint of the study, than a placebo nasal spray in the cohort of participants aged 45 years and over (N=118, p=0.017).
The reduction in viral load for Viraleze™ was also statistically significant compared with placebo for the cohorts of participants aged 50 and over (N=101, p=0.018), 55 and over (N=84, p=0.024), 60 and over (N=66, p=0.003), and 65 and over (N=50, p=0.005). Notably, the magnitude of the reduction in viral load by Viraleze™ compared with placebo increased with age.
Viraleze™ reduced SARS-CoV-2 viral load in the nose by 80% from baseline in less than 24 hours after starting dosing in the group of patients aged 65 and over, whereas viral load in the placebo group remained unchanged from baseline to day 2 (p=0.008).
Viraleze™ reduced viral load compared with placebo in the full study population including all patient age groups (N=197), although this difference was not statistically significant. Of note, treatment compliance and vaccination rates were lowest in participants aged under 40.
Dr Stephen Winchester, Consultant Medical Virologist at Frimley Health NHS Foundation Trust and Principal Investigator of the Viraleze™ clinical study at Ashford and St Peter’s Hospitals NHS Foundation Trust in the UK, commented:
“I am very impressed by these clinical data demonstrating the ability of Viraleze nasal spray to accelerate SARS-CoV-2 RNA clearance and recovery from clinically important symptoms such as anosmia in these fully vaccinated participants with COVID-19.
“The positive SARS-CoV-2 RNA clearance outcomes and evidence of clinical benefit in cohorts of older participants indicate that Viraleze could potentially be of significant benefit in people over 45 years of age to support their vaccine responses.
“Viraleze was very well tolerated and demonstrated no increase in side effects compared with the placebo.
“Based on these data, Viraleze, which is a broad-spectrum nasal spray, could have clinical benefit for protection against infection and treatment of individuals, as well as infection control of populations.”
The significant reduction in viral load achieved with Viraleze™ in older age groups in this clinical study has particular relevance for older age groups in the wider population and potentially for immunocompromised groups, such as patients receiving chemotherapy or other immunosuppressive treatments and transplant recipients. Older age groups can be more susceptible to respiratory infections and disease due to the gradual weakening of the immune system with age and underlying health conditions[4],[5]. In the Viraleze™ study, 60% of participants were aged 45+, representing a significant proportion of the study population.
The study also demonstrated a more rapid rate of viral clearance for Viraleze™, leading to an approximately 66% greater reduction in viral load compared with placebo between days 2 and 6 of treatment in participants of all ages, and the difference was statistically significant (-0.66 vs -0.54 logs per day, respectively, p=0.035, N=197).
Viral load and viral clearance rate are clinically important determinants of the severity and prognosis of respiratory viral infections, including SARS-CoV-2, and have been shown to be key drivers of transmission[6],[7].
The time to recording a negative SARS-CoV-2 PCR test was faster for Viraleze™ compared with placebo in all cohorts of 45, 50, 55, 60 and 65 years of age and older, and these differences were statistically significant (p values [log rank] ranging from 0.014 to 0.048).
COVID-19 Symptoms
Although most participants in the study had a mild form of COVID-19, likely as a result of being vaccinated, the proportion of participants with resolution of COVID-19 symptoms was higher for Viraleze™ compared to placebo across all categories of symptoms assessed (i.e., nose, throat, eyes, chest/respiratory, gastrointestinal and systemic)[8], but not statistically significant.
Loss of smell (anosmia), a common side effect of COVID-19 that also occurs in some other respiratory infections, such as influenza, is related to damage to the olfactory sensory neurons following viral infection[9]. Loss of smell resolved more rapidly in participants using Viraleze™ compared with placebo. The percentage of participants reporting a loss of smell at any time after starting study treatment was also markedly lower in the Viraleze™ group compared with placebo. These differences were statistically significant in participants aged 55 and over (28.9% vs 51.1%, p=0.047) and 65 and over (18.2% vs 51.9%, p=0.019). Differences were borderline significant in the age groups 45+, 50+ and 60+.
After 7 days of using Viraleze™, the percentage of participants reporting continued loss of smell at Day 8 was markedly lower in the Viraleze™ group compared with the placebo group (see Figure 1).
%20before%20treatment%20and%20at%20Day%208%20by%20age%20group.PNG)
Figure 1. Percentage of participants with loss of smell (anosmia) before treatment and at Day 8 by age group
In participants aged 55 and over and 60 and over who had throat-related symptoms (scratchy or itchy throat, sore or painful throat and difficulty swallowing) at baseline, the proportion of Viraleze™ participants with resolution of these symptoms at day 8 was significantly higher compared to placebo (55+: 83.9% vs 56.4%, p=0.020; 60+: 86.4% vs 54.8%, p=0.019).
Professor George Kinghorn OBE MD FRCP, retired Consultant Physician and Clinical Research Director in Communicable Diseases, and Starpharma’s independent medical representative for the Viraleze™ study, commented:
“These clinical data for Viraleze are very promising and indicate a consistent antiviral effect most significant in people aged 45 years and over. The antiviral effects of Viraleze, including reduced viral load and more rapid viral clearance, are of potential importance in reducing the transmission of infections. The study results also provide evidence of clinical benefit of Viraleze in terms of reduced duration of symptoms, particularly in the older age groups. The safety results indicate that Viraleze is very well tolerated and without significant adverse events.
“While Viraleze has the potential to help protect people from becoming infected with SARS-CoV-2 and other respiratory infections, the demonstration of a significant treatment benefit in participants already infected with COVID-19 is encouraging.
“Collectively, the efficacy and safety results indicate a favourable risk-benefit profile for Viraleze.”
Safety Results
The study also confirmed the favourable safety profile of Viraleze™. Adverse events (AEs) were reported in 16/109 (14.7%) of Viraleze™ participants and 15/113 (13.3%) of placebo participants. The vast majority of AEs in each group were of mild severity, and very few participants (4/222, 1.8%) had AEs that were considered possibly related to study treatment with either Viraleze™ or placebo.
Starpharma’s Chief Executive Officer, Cheryl Maley, commented:
“The clinical study on Viraleze™ has shown positive antiviral efficacy in participants with COVID-19. These results are consistent with Starpharma’s nonclinical studies, which also demonstrated that Viraleze™ protected against infection in a humanised mouse challenge model of COVID-19.
“SPL7013 in Viraleze™ has also been shown to have virucidal effects against all tested strains of SARS-CoV-2, including recently identified variants, with reductions of over 99.9% of infectious virus in laboratory studies. Viraleze™ has also demonstrated significant antiviral effects in vitro against a wide range of other respiratory viruses, including influenza viruses, respiratory syncytial virus (RSV), and common cold viruses, including human coronaviruses. Starpharma is grateful to the Principal Investigator of the study, Dr Stephen Winchester, and the Research and Development team at St Peter’s Hospital in the UK for their efforts in conducting the study, as well as all the participants who took part in the study, for their time and effort in contributing to valuable scientific research.”
