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Xylitol Based Nasal Spray for COVID-19 Treatment

Primary Purpose

Respiratory Viral Infection

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Nasal Spray
Sponsored by
Xlear, Inc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Respiratory Viral Infection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Capable of understanding and providing signed informed consent and ability to adhere to the requirements and restrictions of this protocol; Adult aged ≥18 years old with at least two comorbidities: diabetes (type 1 &2), obesity (BMI >30), hypertension, chronic heart disease, chronic pulmonary disease, chronic liver disease. Internet access and capability and willingness to participate in audio or audio/video engagements with medical professionals, receive texts, emails, and phone calls from study staff and have a device and reasonable cellular data or other internet access to submit daily study required information using a smart phone, tablet, laptop, or desktop computer during the study period; COVID-19 infection confirmed with a laboratory SARS-CoV-2 RT-PCR nasal swab; Specimen collected within the past 48 hours; Mild COVID-19 symptoms which may include fever, cough, sore throat, malaise, headache, muscle pain, gastrointestinal symptoms, lack of taste or smell without shortness of breath Exclusion Criteria: Not fit to consent and unable to follow the protocol; Age <18 years; Current tracheostomy or laryngectomy; Hypersensitivity to the active substance or to any of the excipients; Concomitant respiratory therapy such as oxygen or ventilator support. Positive airway pressure for obstructive sleep apnea is permitted if treatment was established with good compliance at least 3 months before enrolment; Need for hospitalisation for any reason; Inability to safely self-administer nasal spray Any clinical contraindications, as judged by the Qualified Medical Practitioner; Clinical signs indicative of moderate, severe or critical COVID severity symptoms (as defined by FDA COVID-19 Guidance Document) Mentally or neurologically disabled patients who are considered not fit to consent to their participation in the study; Lactating, pregnant or planning to become pregnant during the study period; Diagnosed with prior COVID-19 infection (>48 hours from the time the test is reported prior to the time of screening). No relevant comorbidity or only one comorbidity

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Interventional

    Control

    Arm Description

    The participants will receive Xylitol based nasal spray

    The participants will receive saline based placebo

    Outcomes

    Primary Outcome Measures

    Viral load reduction
    The between-groups difference in log-viral load over the total treatment period

    Secondary Outcome Measures

    Undetectable viral load
    Proportion of subjects reaching undetectable viral load
    Hospitalization requirement
    The proportion difference in groups requiring hospitalization
    Reduction of clinical symptoms score
    Measurement of modified Jackson score
    Tolerability of Nasal Spray
    Adverse events and discontinuation of nasal spray use
    Safety of Nasal Spray
    Adverse events

    Full Information

    First Posted
    November 15, 2022
    Last Updated
    November 19, 2022
    Sponsor
    Xlear, Inc
    Collaborators
    Metanoic Health Ltd.
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05618483
    Brief Title
    Xylitol Based Nasal Spray for COVID-19 Treatment
    Official Title
    Clinical Efficacy of Xylitol Based Nasal Spray for the Treatment of Mild COVID-19 Infection
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    November 28, 2022 (Anticipated)
    Primary Completion Date
    December 31, 2023 (Anticipated)
    Study Completion Date
    June 30, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Xlear, Inc
    Collaborators
    Metanoic Health Ltd.

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Xlear have developed and patented a xylitol containing nasal spray for the treatment of upper-respiratory tract infections. The nasal spray is comprised of xylitol and GSE (Grapefruit Seed extract) which provides antibacterial properties as well as preventing viral adhesion in the nasal passage. Studies into Xlear's antiviral effects on SARS-CoV-2 are currently ongoing but hypothetically, a Xylitol Based Nasal spray may prove to be a useful and inexpensive treatment for COVID-19 infection.
    Detailed Description
    1. BACKGROUND and RATIONALE In the wake of the Coronavirus disease 2019 (COVID-19) pandemic, worldwide healthcare has rapidly evolved in response. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel virus responsible for COVID-19, which at the most severe end of the spectrum of disease can require hospitalisation or ICU admission. Preventative measures are currently being taken with numerous vaccination programs across the world. However, there is currently no established treatment for mild COVID-19 infection, i.e., symptomatic infection not requiring hospitalisation, which makes up a significant proportion of cases. Xylitol has shown promising results in combating SARS-CoV-2 in vitro and this study aims to explore whether Xlear's Xylitol based Nasal Spray has an effect in vivo. 1.1 COVID-19 Infection SARS-CoV-2 is a positive-sense, single-strand RNA virus comprised of four structural proteins: Nucleocapsid (N) protein, Membrane (M) protein, Spike (S) protein and Envelope (E) protein. These structural proteins play an important role in receptor binding, transcription, replication and assembly of the virus in host cells (Boopathi et al., 2020). The nasal epithelium acts as the primary site for SARS-CoV-2 binding to angiotensin converting enzyme-2 (ACE2) - the receptor responsible for COVID-19 infection (Zhou et al., 2020). With nasal carriage playing a vital role in transmission, drugs administered intranasally could be a viable therapeutic option (Sungnak et al., 2020). 1.2 Drug: Xylitol Xylitol is a sugar alcohol derived from plants. It is used in the dental profession to prevent plaque build-up and inhibit enamel demineralisation by interfering with the metabolism of Streptococcus mutans, causing cell death and thus preventing dental caries (Janakiram et al., 2017). Xylitol not only demonstrates antimicrobial behaviour but can also modulate immunity and contribute to wound healing (Salli et al., 2019). 1.2.1 Xylitol and Respiratory Tract Infections Xylitol's inhibitory effect on Streptococcus mutans growth has prompted more research into its interactions with other nasopharyngeal pathogens responsible for respiratory tract infections. An in vitro study into alpha-haemolytic Streptococcus pneumoniae and beta-haemolytic Streptococci treated with 1% and 5% xylitol showed statistically significant inhibition of growth over a 24-hour incubation period (Kontiokari et al., 1999). Another team established xylitol's ability to kill coagulase-negative Staphylococcus. 5% xylitol administered to 21 participants compared to a control group using a saline solution showed a significant decrease in Staphylococcus count from 597 colony forming units (CFU) per swab to 99 CFU per swab (Zabner et al., 2000). 1.2.2 Xylitol and Viruses Xylitol's inhibitory effects on bacteria are well documented but little is known regarding its antiviral properties. Dietary xylitol was used to treat influenza A virus in vivo. Mice given a combination of xylitol and red ginseng had 100% survival rate at 33mg/kg/day of xylitol and 60% survival rate at 3.3mg/kg/day after day 14 of infection versus 0% survival rate on PBS (control), red ginseng and xylitol separately. This suggests a synergistic effect between xylitol and red ginseng (Yin et al., 2014). A study into xylitol and its interactions with human respiratory syncytial virus (hRSV) was conducted in 2015. Xylitol was tested in vitro on a hRSV suspension and in vivo in mice. The in vitro effect of xylitol showed complete inhibition at concentrations of 3.13mg/ml. Xylitol significantly reduced lung viral titres in mice with 3.3mg/kg/d proving the most effective dose (Xu et al., 2016). 1.3 Grapefruit Seed Extract (GSE) Grapefruit seed extract (GSE) is made from grapefruit seeds. It is used as a natural remedy due to its antioxidant and antimicrobial properties (Reagor et al., 2002; Salehi et al., 2019). 1.3.1 GSE and Viruses GSE was tested on multiple viruses to determine if it had any inhibitory effects. GSE exhibited virucidal activity against avian influenza virus (AIV) and Newcastle disease virus (NDV) but not against infectious bursal disease virus (IBDV) (Komura et al., 2019). These findings may be important as AIV and NDV are enveloped viruses like SARS-CoV-2 whilst IBDV is not (Schoeman et al., 2019). It could be hypothesised that GSE could exhibit similar inhibition on SARS-CoV-2. 1.4 Xlear's Xylitol based Nasal Spray Xlear have developed and patented a xylitol containing nasal spray for the treatment of upper-respiratory tract infections. The nasal spray is comprised of xylitol and GSE which provides antibacterial properties as well as preventing viral adhesion in the nasal passage. Studies into Xlear's antiviral effects on SARS-CoV-2 are currently ongoing but hypothetically, a Xylitol Based Nasal spray may prove to be a useful and inexpensive treatment for COVID-19 infection. 1.4.1 Xlear and Coronavirus Xylitol has been shown to exhibit antiviral properties against SARS-CoV-2 in vitro (Bansal et al., 2021; Ferrer et al., 2020). USA-WAI/2020 strain was prepared and passaged in Vero 76 cells for testing with Xlear (experiment 2) and its components xylitol and GSE separately (experiment 1). GSE 0.2% reduced SARS-CoV-2 from 3.67 log10 CCID50/0.1 mL to undetectable in experiment 1. Xlear in virucidal assays completely inhibited viral infectively at varying concentrations (90%, 80%, 50%) and reduced viral titre by 2.17 log in 20% concentration indicating a dose-dependent response (Appendix 1) (Ferrer et al., 2020). A subsequent study showed statistically significant reduction in viral titres treated with Xlear nasal spray treatment - 4.2 log10 CCID50/0.1mL to 1.7, a reduction of 2.5 log10 CCID50 (Cannon et al., 2020). A recent private report by Dr Cagno's team in Lausanne (April 2021) has confirmed the viral killing properties of Xlear in 2021 SARS-CoV-2 strains. Viral stocks were grown in Vero E6 cells belonging to two lineages, B1.1.7 and B1.351. Complete inhibition of viral infectivity was observed in 90%, 60% and 20% concentration Xlear virucidal assays for B1.351. Viral infectivity was similarly completely inhibited in B1.17 at 90% and 60% concentration with a 3.06 log reduction at 20% illustrated in Appendix 2. A case study was conducted on individuals who had taken Xlear as treatment for COVID-19 infection. Participants were required to spray into each nostril four times per day (140 µL per spray). All individuals showed improvement in symptoms with quicker turnarounds from turning positive to negative via COVID-19 reverse transcriptase polymerase chain reaction (RT-PCR) nasal swabs. Importantly, some individuals had relevant co-morbidities such as current smoking status and obesity. Although it is difficult to attribute symptom improvement and viral load decrease to Xlear's spray, it does provide rationale for a double-blind placebo controlled randomised clinical trial (Go et al., 2020).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Respiratory Viral Infection

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Randomization to Nasal Spray or Placebo
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Masking Description
    Subjects will be randomized 1:1 to receive the Xylitol Based Nasal Spray or a matching saline base placebo. This is a double blinded study. The Nasal Spray Kits will be randomized and allocated to patients in chronological order.
    Allocation
    Randomized
    Enrollment
    80 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Interventional
    Arm Type
    Experimental
    Arm Description
    The participants will receive Xylitol based nasal spray
    Arm Title
    Control
    Arm Type
    Placebo Comparator
    Arm Description
    The participants will receive saline based placebo
    Intervention Type
    Device
    Intervention Name(s)
    Nasal Spray
    Other Intervention Name(s)
    Xlear nasal spray
    Intervention Description
    The nasal spray is made of xylitol and grapefruit seed extract. The spray is antiviral, but there is no data of its clinical efficacy against Covid-19.
    Primary Outcome Measure Information:
    Title
    Viral load reduction
    Description
    The between-groups difference in log-viral load over the total treatment period
    Time Frame
    Day 0 (baseline), Day 2, 4 6 and 8
    Secondary Outcome Measure Information:
    Title
    Undetectable viral load
    Description
    Proportion of subjects reaching undetectable viral load
    Time Frame
    baseline to Day 2, 4, 6 and 8
    Title
    Hospitalization requirement
    Description
    The proportion difference in groups requiring hospitalization
    Time Frame
    Baseline through Day 8
    Title
    Reduction of clinical symptoms score
    Description
    Measurement of modified Jackson score
    Time Frame
    Baseline through Day 14
    Title
    Tolerability of Nasal Spray
    Description
    Adverse events and discontinuation of nasal spray use
    Time Frame
    Baseline through Day 14
    Title
    Safety of Nasal Spray
    Description
    Adverse events
    Time Frame
    Baseline through Day 14

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Capable of understanding and providing signed informed consent and ability to adhere to the requirements and restrictions of this protocol; Adult aged ≥18 years old with at least two comorbidities: diabetes (type 1 &2), obesity (BMI >30), hypertension, chronic heart disease, chronic pulmonary disease, chronic liver disease. Internet access and capability and willingness to participate in audio or audio/video engagements with medical professionals, receive texts, emails, and phone calls from study staff and have a device and reasonable cellular data or other internet access to submit daily study required information using a smart phone, tablet, laptop, or desktop computer during the study period; COVID-19 infection confirmed with a laboratory SARS-CoV-2 RT-PCR nasal swab; Specimen collected within the past 48 hours; Mild COVID-19 symptoms which may include fever, cough, sore throat, malaise, headache, muscle pain, gastrointestinal symptoms, lack of taste or smell without shortness of breath Exclusion Criteria: Not fit to consent and unable to follow the protocol; Age <18 years; Current tracheostomy or laryngectomy; Hypersensitivity to the active substance or to any of the excipients; Concomitant respiratory therapy such as oxygen or ventilator support. Positive airway pressure for obstructive sleep apnea is permitted if treatment was established with good compliance at least 3 months before enrolment; Need for hospitalisation for any reason; Inability to safely self-administer nasal spray Any clinical contraindications, as judged by the Qualified Medical Practitioner; Clinical signs indicative of moderate, severe or critical COVID severity symptoms (as defined by FDA COVID-19 Guidance Document) Mentally or neurologically disabled patients who are considered not fit to consent to their participation in the study; Lactating, pregnant or planning to become pregnant during the study period; Diagnosed with prior COVID-19 infection (>48 hours from the time the test is reported prior to the time of screening). No relevant comorbidity or only one comorbidity
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Isaac John, PhD
    Phone
    +447798566612
    Email
    Isaac.John@metanoichealth.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Ahsan W Rathore, MBBS
    Organizational Affiliation
    University of Health Sciences Lahore
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Saqib Mahmood, MBBS PhD
    Organizational Affiliation
    University of Health Sciences Lahore
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
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    34797868
    Citation
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    URL
    http://www.biorxiv.org/content/10.1101/2020.11.23.394114v1.abstract
    Description
    Ferrer, G., Betancourt, A., Go, C., Vazquez, H., Westover, J., Cagno, V., Tapparel, C. and Sanchez-Gonzalez, M. A Nasal Spray Solution of Grapefruit Seed Extract plus Xylitol Displays Virucidal Activity Against SARS-Cov-2 In Vitro. bioRxiv

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    Xylitol Based Nasal Spray for COVID-19 Treatment

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