Clinical Trial of Efficacy and Safety of ММН-407 in the Treatment of Influenza in Outpatient Adults

• Status: Recruiting
• Trial end date: 2022-12-01
• Target enrollment: 0
• Participant gender: All

Summary

The main purpose of this study is:

• to evaluate the efficacy and safety of MMH-407 in the treatment of influenza in outpatient adults.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Materia Medica Holding

Criteria

Inclusion Criteria:

1. Patients of male and female gender aged 18 to 64 years.

2. Uncomplicated, moderate influenza supported by all the symptoms:

• axillary temperature ≥38.1°С on physician examination;

• at least one moderate general symptom of influenza infection (headache, fever/chill, aches in the muscles/joints, weakness/drowsiness);

• at least one moderate respiratory symptom of influenza infection (cough, sore throat, or nasal congestion).

3. Positive influenza rapid test (detection of virus antigens in the nasal epithelium).

4. First 24 hours of the onset of illness.

5. Patients who agree to use a reliable method of birth control during the study.

6. Patients who have provided signed Participant Information Sheet and Informed Consent form to participate in a clinical trial.

Exclusion Criteria:

1. Severe influenza infection that requires hospitalization.

2. Suspected pneumonia or bacterial infection (including otitis media, sinusitis, urinary tract infection, meningitis, sepsis, etc.) that requires the use of antibiotics, starting from the first day of illness.

3. Suspected early manifestations of a condition that, on its first onset, produces symptoms similar to those of influenza (other infectious diseases and/or influenza-like syndrome associated with the first onset of a systemic connective tissue disorder or another condition).

4. Patients who require the use of antivirals that are not permitted during the study.

5. Current season influenza vaccination.

6. Prior history or diagnosis of primary or secondary immunodeficiency

7. Patients with any known or suspected malignant neoplasm.

8. An exacerbated or decompensated chronic disease interfering with the subject's participation in the clinical trial.

9. Malabsorption syndrome, including congenital or acquired lactase deficiency (or any other disaccharidase deficiency), and/or galactosemia.

10. Current allergy to or intolerance of the active substances or any of the excipients in the medications used in the treatment.

11. Pregnancy, breast-feeding, childbirth within less than 3 months prior to the inclusion in the trial, or unwillingness to use contraceptive methods during the study

12. Prior history of non-adherence to medication; mental disorder; or alcohol or substance abuse, which, in the investigator's opinion, will compromise compliance with study procedures.

13. Use of any of the "Prohibited Concomitant Medications" within 2 weeks prior to study entry.

14. Patients who, as judged by the investigator, will fail or be unwilling to comply with the observation requirements or adhere to the dosing regimen during the study.

15. Participation in other clinical studies within 3 months prior to the inclusion in this study.

16. Patients who are related to any of the on-site research personnel directly involved in the conduct of the study or are an immediate relative of the investigator. 'Immediate relative' means husband, wife, parent, son, daughter, brother, or sister (regardless of whether they are natural or adopted).

17. Patients who work for OOO "NPF "Materia Medica Holding" (i.e. company employees, temporary contract workers, designated officials responsible for carrying out the research or any immediate relatives of the aforementioned).