Study of Ingaron's Effect on Efficacy and Resistance to Antibiotics in Community-acquired Pneumonia

• Status: Completed
• Trial end date: 2019-05-30
• Target enrollment: 0
• Participant gender: All

Summary

The primary purpose of this study is to effect of Ingaron®, a lyophilisate for the preparation of a solution for intramuscular and subcutaneous administration of 100,000 IU (LLC NPP Farmaklon, Russia) on the effectiveness of antibiotic therapy in patients with community-acquired pneumonia who fell ill during the epidemiological rise of ARVI.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: SPP Pharmaclon Ltd.
• Treatments: Interferon-gamma; Interferons

Criteria

Inclusion Criteria:

1. Patients of the inpatient department of both sexes aged 18 to 60 years.

2. Confirmed diagnosis - community-acquired pneumonia (causative agent not specified) of an uncomplicated typical course without respiratory failure and the duration of symptoms is not more than 14 days.

3. Risk class of lethal outcome I-II according to the Fine scale.

4. Availability of an Informed Consent voluntarily signed by the patient.

Exclusion Criteria:

1. Increased individual sensitivity to gamma interferon, Ingaron® and / or excipients that are part of Ingaron® or drugs used in antibacterial therapy.

2. The use of immunomodulating, immunostimulating or immunosuppressive therapy later than 1 month before enrollment in the study.

3. Bronchial asthma and/or COPD.

4. Congestive heart failure.

5. Acute diseases of the gastrointestinal tract or other pathologies that may affect the absorption, distribution, metabolism or excretion of drugs.

6. Chronic liver and / or kidney disease or other pathologies that may affect the absorption, distribution, metabolism or excretion of drugs.

7. Oncological diseases, autoimmune, immunosuppressive conditions at present or according to history.

8. Cerebrovascular pathologies.

9. Diabetes.

10. Pregnancy or lactation.

11. Smoking index over 10 pack/years.

12. Data on severe nervous or mental diseases, including history.

13. Violation of consciousness.

14. Participation of the patient in other studies with the use of drugs or other methods of therapy, including clinical, currently or later than 1 month before inclusion in the study.