Efficacy and Safety of Enisamium Iodide for the Treatment of Acute Respiratory Viral Infections, Including Influenza.

Human Influenza Clinical Trial

Official title:

A Prospective Single-blind Comparative Clinical Study of Efficacy and Safety of Amizon 0.25 g Tablets, Manufactured by Farmak JSC, in Patients With ARVI, Including Influenza.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04682444
• Other study ID #: AM-STP-2-2008
• Status: Completed
• Phase: Phase 2/Phase 3
• Start date: April 13, 2009
• Est. completion date: May 15, 2010

Study information

• Verified date: December 2020
• Source: Joint Stock Company "Farmak"
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This randomized, single blind clinical study was conducted to investigate the clinical efficacy and safety of the drug Amizon (enisamium iodide), in comparison with placebo for the treatment of patients with acute respiratory viral infections (ARVI), including influenza. Enisamium iodide is an antiviral small molecule. Adult patients were enrolled and randomised into 2 groups. On the first day of the onset of symptoms of ARVI, one group of patients took Amizon tablets (active ingredient enisamium iodide) for 7 days; the other group of patients took matching placebo tablets for 7 days. Examination and observation of all participants was done for up to 14 days after the first intake of the study drug. The effect of treatment was assessed by subjective reporting of the symptoms of ARVI and influenza, using a predefined symptom scale score system. Objective assessment was performed by measuring vitals signs, laboratory tests (including blood and urine assessment), as well as evaluating the immune status (including measuring the relative concentration of interferon and immunoglobulins).

Description:

Numerous studies have shown that influenza vaccines, prepared against the relevant epidemic seasonal vaccine strains, are an effective remedy in prevention of this mass disease and are able to protect about 80% of otherwise healthy children and adults. However, to develop vaccines against the emerging new pandemic strain of the influenza virus and produce them in the necessary amounts requires at least 6 months. During such interim periods, sufficient protection of the population is essential by effective measures for treatment and prevention of influenza. This randomized, single-blind, clinical study was conducted to investigate the clinical efficacy and safety of the drug Amizon (N-methyl-4-benzylcarbamidopyridinium iodide, international nonproprietary name enisamium iodide) compared with placebo, for the treatment of patients with ARVI, including influenza. Enisamium iodide is an antiviral small molecule. Enisamium can directly inhibit influenza viral RNA replication. The study design was: randomised, single-blind, 2 parallel groups. Adult patients (18-60 y) with symptoms of ARVI, including influenza took either Amizon tablets (active ingredient enisamium iodide) for 7 days; in the control group patients took placebo tablets for 7 days. Study visits occurred on Day 0 (screening, examination, check inclusion/exclusion criteria, enrollment, randomization, and first intake of study drug); further study visits were on Day 3, Day 7, and Day 14. The effect of treatment was assessed by questioning the patients regarding ARVI and influenza symptoms that included pain, headache, general weakness, sore throat, pain in the joints, fatigue, runny and itchy nose. The severity of symptoms was recorded using a 4-point Likert scale. Further evaluation of the treatment was performed by measuring the vitals signs, laboratory tests that included blood and urine analysis, biochemical analysis, as well as assessing the immune status (including measuring the absolute lymphocytes count, and evaluating the relative concentration of interferon (IFN)-alpha and IFN-gamma, and immunoglobulins (IgA, IgM, and IgG).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 100
• Est. completion date: May 15, 2010
• Est. primary completion date: January 28, 2010
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• Patients aged between 18 to 60 years
• Patients with ARVI, including influenza, starting not later than for 1 day prior to

inclusion in the study:

• The body temperature measured axillary above 37.2 °C
• Presence of one of the signs of respiratory disease (runny nose, cough, pain / tickling in the throat)
• Presence of one of the systemic symptoms (weakness, myalgia, headache , chills, sweating)
• Provide written informed consent
• Ability to understand the nature of the study and provide written informed consent in accordance with Good Clinical Practice (GCP) and local law

Exclusion Criteria:

• Age over 60 years and under 18 years old
• Presence of allergic reactions
• Intolerance to NSAIDs and iodine-containing drugs
• Hypersensitivity to the components of the drug
• Mental illness that impedes compliance with the research procedure
• Pregnancy or breast-feeding
• Presence of acute, clinically significant respiratory and cardio vascular insufficiency, functional disorders of liver, kidney, digestive tract (ulcer disease) determined at physical examination or by laboratory screening tests
• Presence of congenital defects or serious chronic disease of the lungs, kidneys, cardiovascular system, nervous system, metabolic disorders, psychiatric disorders, confirmed by patients history or during initial examination
• The use of preparations of blood cytokine immunoglobulin in for 3 months prior to the study
• Chronic use of alcohol and / or drugs
• Presence or history of cancer diseases, HIV, hepatitis B and C
• Application of immunosuppressive or immunomodulatory drugs for 6-months prior to the study
• Women of child-bearing potential and who do not use acceptable measure of contraception or do not plan to use those throughout the study
• Any clinical condition that, according to the investigator, will not allow to safely carry out the protocol and take the studied drugs without risk to health
• Patients receiving antiviral therapy,
• Participation in other clinical trials at the present time or during the last 3 months.

Related Conditions & MeSH terms

• Acute Respiratory Viral Infections
• Human Influenza
• Infection
• Influenza, Human
• Virus Diseases

Intervention

Drug:
• Enisamium Iodide
Patients ingested Amizon tablets after meal without chewing as follows: 2 tablets (total dose 0.5 g) 3 times a day, for 7 days. Each tablet contains 0.25 g of Nmethyl- 4-N-methyl-4-benzylcarbamidopyridinium iodide (INN enisamium iodide).
• Placebo
Patients ingested placebo tablets after meal without chewing in the dose 0.5 g (2 tablets), 3 times a day, for 7 days.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Joint Stock Company "Farmak"

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Efficacy - Clinical improvement from Day 3 after therapy start	Evaluate the number of patients in the treatment and the placebo groups regarding clinical improvement from Day 3 after therapy start.; Clinical improvement was assessed by the investigator from scores of objective and subjective data, relating to the severity of clinical symptoms of ARVI, including influenza.; Objective symptoms were assessed using the following score system: normal or abnormal blood pressure was counted 0 or 4 score points; lung auscultation was counted 0 for vesicular breath sound and wheezing or crepitation were scored 2 or 4 points, respectively; clear and rhythmic heart sounds were each scored 0 points, whereas noisy and arrhythmic heart sounds were scored 2 points each.; The subjective symptoms were assessed using a 4-point Likert scale, ranging from 1 (absent) to 4 (severe).	Day 0, 3, 7, 14
Secondary	Efficacy - Time of disappearance of respiratory tract affection symptoms	Evaluate the time of disappearance of respiratory tract symptoms (rhinitis, pharyngitis, laryngitis, tracheitis, bronchitis, cough).; Evaluate the general state of health, condition of cutaneous coverings, oral mucosa and tonsils, peripheral lymph nodes, abdominal cavity organs, nervous and musculoskeletal system, lung and heart percussion and auscultation data were assessed.; Evaluate the intensity and duration of the disease symptoms: temperature response, catarrhal events in nasopharynx and other respiratory tract parts.; Clinical improvement was assessed by the visit day on which the symptoms were absent (score 1 on the Likert scale, as described for Outcome 1).	Day 0, 3, 7, 14
Secondary	Efficacy - Body temperature normalization	Monitor body temperature.	Day 0, 3, 7, 14
Secondary	Efficacy - General symptoms of ARVI including influenza	Time of disappearance of general symptoms -- ARVI, including influenza.; Time of disappearance of general symptoms relating to the respiratory tract, including weakness, headache, myalgia, chills, sore throat, and cough.	Day 0, 3, 7, 14
Secondary	Efficacy - Viral antigens	Viral antigens evaluated: influenza A and B, respiratory syncytial virus, adenovirus, parainfluenza virus.; Virus antigens were isolated from nasal swabs and detected by using validated immunofluorescence testing methods.; Efficacy assessment: evaluate viral antigen levels at the end of treatment (Day 7) versus the baseline data (Day 0) and compare with the placebo group.	Day 0, 3, 7
Secondary	Safety - Adverse events	Adverse events occurring during the study were recorded daily by the patients into a patient dairy (Day 0 to Day 14). Clinically relevant laboratory parameters changes outside the normal range were also considered as adverse events.; The relationship of the adverse events to the intake of the investigational drug assessed by the investigator.	Day 0 to Day 14
Secondary	Safety - Laboratory parameters - Immune status	Assessment of the immune status was performed by evaluating the concentration in blood serum of interferon [IFN]-alpha and IFN-gamma, immunoglobulin A, immunoglobulin M, immunoglobulin G.; Determination of immunoglobulins ?, ?, G was performed by turbidimetry. Determination of interferon-alpha and interferon-gamma in human blood serum was carried out using flow cytometer.	Day 0, 7, 14