Study on Performance and Safety of Sentinox in the Prevention of Acute Respiratory Infections (ARI)

Post-market, Randomized and Controlled Clinical Study to Assess the Performance and Safety of Sentinox in the Prevention of Acute Respiratory Infections

This is a post market, single-center, randomized, controlled, clinical study to assessTo evaluate the performance of self-administered Sentinox intranasal spray in preventing ARI caused by at least one respiratory virus

Study Overview

• Status: Recruiting
• Conditions: Healthy Volunteers
• Intervention / Treatment: Device: Sentinox

Detailed Description

The study will consist of:

• A screening visit (Visit 0, on-site) to sign the informed consent form (ICF). The operator will:

  o review the inclusion/exclusion criteria

  o record the medical history, demographic data and concomitant medications (CMs), including previous anti-influenza, anti-COVID-19 and anti-pneumococcal vaccinations

• A randomization visit (Visit 1, on-site) to start the surveillance period. As soon as an increase in the regional epidemiological curve of ARI is observed, screened subjects will be invited for Visit 1. At Visit 1 the operator will:

  • check that the inclusion/exclusion criteria are still met, to confirm eligibility
  • confirm the medical history and the concomitant medications including previous anti-influenza, anti-COVID-19 and anti-pneumococcal vaccinations
  • record the result of the pregnancy testing

  • randomize with a 1:1 ratio in one of 2 trial Groups: - Group A: treatment with Investigational Medical Device (IMD) performed 3 times/day for 21 days at 8 am, 2 pm and 8 pm

    - Group B: no IMD treatment

  • invite the subjects to start: - treatment and surveillance period for 21 days, if belonging to Group A

    • surveillance period for 21 days, if belonging to Group B At Visit 1, an e-diary access will be delivered to both Groups to daily record Adverse Events (AEs), CMs other than treatments recorded in V1, presence of clinical features of ARI and IMD usage. The regular usage of the IMD will be recorded daily, as well as any change of the device and the reason for this. Study participants will install the Mobile App to complete the e-diary and will receive instructions to use the app. They will be instructed not to disclose their assignment to the treatment group to the blinded Investigator.

The IMD bottles needed for the 21-days treatment will be delivered to the enrolled participants of Group A, who will be trained to self-administer the treatment.

• A surveillance 21-days period, during which:

• the subjects of Group A will perform the daily treatment for 21 days
• the subjects of Group A and B will fill in a daily e-diary; the subjects will receive a reminder to follow the therapy (in the morning) and to complete the e-diary (in the evening)
• as soon as the subject records at least one symptom of ARI (i.e., cough, sore throat, shortness of breath, coryza as described in the European Commission guideline on relevant case definitions of communicable diseases [Commission Implementing Decision (EU) 2018/945 of 22 June 2018]) in the Mobile App, the blinded Investigator will be advised and will contact the subject by telephone within 12 hours to verify that the illness is due to ARI and to accordingly update the eCRF.

If during the phone contact the blinded Investigator judges the symptoms as correlated to ARI:

• the subject will be invited to immediately stop the IMD treatment if belonging to Group A
• the subject will be invited to the site for Visit 2 within 24 hours to perform a nasopharyngeal swab and to interrupt the surveillance period (Group A and B).

If during the phone contact the blinded Investigator judges the symptoms as not correlated to ARI, the subject will continue the surveillance period and the IMD treatment (if belonging to Group A) till a maximum of 21 days.

• A final visit (Visit 2, on-site). The subject, whose symptom of ARI during the surveillance period has been confirmed by the Investigator during the phone call, will attend for a site visit and be requested to:

• have a nasopharyngeal swab taken
• undergo a physical examination
• fill in the Visual Analogue Scale (VAS) score for Sentinox tolerability (for subjects of Group A)
• complete a 5-points Likert Scale for the satisfaction of Sentinox (for subjects of Group A)
• return the used and unused treatment bottles (for subjects of Group A)

The subject who does not have any symptom of ARI during the surveillance period, will perform a visit within 21±7 days from Visit 1 to:

• fill in the VAS score for Sentinox tolerability (for subjects of Group A)
• complete a 5-points Likert Scale for the satisfaction of Sentinox (for subjects of Group A)
• return the used and unused treatment bottles (for subjects of Group A) At Visit 2, the Mobile App will be uninstalled from the electronic device used by the subjects.

• Study Type: Interventional
• Enrollment (Estimated): 1458
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Giorgio Reiner; Phone Number: +41 (0)91 6957020; Email: giorgio.reiner@apr.ch
• Study Contact Backup: Name: Giancarlo Icardi, PR; Phone Number: +39 010 555 2375; Email: icardi@unige.it

Study Locations

• Italy
  • Genova, Italy, 16132
    • Recruiting
    • Ospedale Policlinico San Martino IRCCS
    • Contact: Giancarlo Icardi, Prof; Phone Number: 0039 010 555 2375; Email: icardi@unige.it

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 14 years to 59 years (Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

1. ICF signed.
2. Males and females aged ≥ 18 years and <64 years at the time of the signature of the ICF.
3. Subjects who are willing to comply with the requirements of the study protocol, attend scheduled visits and calls for the duration of the study by telephone contact and install the Mobile App to use the e-diary.

Exclusion Criteria:

1. Reporting of any symptoms of ARI in the 15 days preceding the Visit 1.
2. Reporting the intake of any drugs, among antiviral or antibacterial therapies, that may interfere with the study results in the 15 days preceding the Visit 1.
3. Presence of any relevant organic, systemic or metabolic disease (particularly significant history of cardiac, renal, neurological, psychiatric, oncology, endocrinology, metabolic or hepatic disease).
4. Immune system illnesses.
5. Known drug and/or alcohol abuse.
6. Individuals who are cognitively impaired and/or who are unable to give informed consent.
7. Ongoing or prior participation in any other clinical trial of an experimental treatment within 30 days from Visit 1.
8. Concurrent or planned treatment with other agents with actual or possible direct antiviral/antibacterial activity.
9. Positive pregnancy test or breastfeeding woman.
10. Known hypersensitivity to the study treatment, its metabolites, or formulation excipient.
11. History of severe drug and / or food allergies.
12. Any condition that, in the opinion of the Investigator, would complicate or compromise the study or well-being of the Subject

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Group A: treatment with Sentinox performed 3 times/day for 21 days; treatment with Investigational Medical Device (IMD) performed 3 times/day for 21 days at 8 am, 2 pm and 8 pm	Device: Sentinox; The treatment will be administered in a dose of 0.5 ml into each nostril (5 sprays) per 3 times/day (8 am, 2 pm and 8 pm), for 21 days from Visit 1.
No Intervention: Group B:no Sentinox treatment

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Performance of self-administered Sentinox intranasal spray in preventing ARI caused by at least one respiratory virus	Measure the proportion of patients with at least one symptoms of ARI (i.e., cough, sore throat, shortness of breath, coryza, as described in the European Commission guideline on relevant case definitions of communicable diseases [Commission Implementing Decision (EU) 2018/945 of 22 June 2018]) and confirmed by positive swab for at least 1 virus.	Daily for a surveillance 21-days period

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Performance of Sentinox in preventing ARI caused by different respiratory viruses	Measure the Proportion of patients with at least one symptom of ARI (i.e., cough, sore throat, shortness of breath, coryza as described in the European Commission guideline on relevant case definitions of communicable diseases [Commission Implementing Decision (EU) 2018/945 of 22 June 2018]) and confirmed by positive swab for each specific strain of virus	Daily for a surveillance 21-days period
Performance of Sentinox intranasal administration against bacterial infection	Measure the Proportion of patients with at least one symptom of ARI (i.e., cough, sore throat, shortness of breath, coryza as described in the European Commission guideline on relevant case definitions of communicable diseases [Commission Implementing Decision (EU) 2018/945 of 22 June 2018]), not confirmed by a positive swab for at least 1 virus, but with positive swab for at least 1 bacterium.	Daily for a surveillance 21-days period
Performance of Sentinox in preventing clinically defined ARI without microbiological confirmation	Measure of Proportion of patients with at least one symptom of ARI (i.e., cough, sore throat, shortness of breath, coryza as described in the European Commission guideline on relevant case definitions of communicable diseases [Commission Implementing Decision (EU) 2018/945 of 22 June 2018]), not confirmed by positive swab for any of the tested virus or bacteria	Daily for a surveillance 21-days period
Subjects' satisfaction of self -administering Sentinox	Measure the product satisfaction of subjects self-administering Sentinox by a 5-points Likert Scale	Daily for a surveillance 21-days period
Tolerability and safety of Sentinox	Measure the Incidence and severity of AEs or incidents related to the use of the nasal solution, hypersensitivity and adverse reactions.	Daily for a surveillance 21-days period

Collaborators and Investigators

• Sponsor: APR Applied Pharma Research s.a.

Study record dates

Study Major Dates

• Study Start (Actual): November 7, 2022
• Primary Completion (Estimated): March 30, 2024
• Study Completion (Estimated): June 1, 2024

Study Registration Dates

• First Submitted: August 8, 2022
• First Submitted That Met QC Criteria: August 10, 2022
• First Posted (Actual): August 12, 2022

Study Record Updates

• Last Update Posted (Actual): October 30, 2023
• Last Update Submitted That Met QC Criteria: October 27, 2023
• Last Verified: October 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Infections; Respiratory Tract Diseases; Respiratory Tract Infections
• Other Study ID Numbers: STX-2022

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No