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NCT05386446

Study of the Use of the Ingaron in Volunteers for the Prevention of COVID-19

Completed Last updated 23 May 2022
What this trial tests

trial testing Interferon gamma human recombinant (IFN-G) in COVID-19 Respiratory Infection in 100 participants. Completed in 15 June 2020.

Timeline
23 April 2020
Primary endpoint
10 June 2020
15 June 2020

Quick facts

Lead sponsorSPP Pharmaclon Ltd.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment100
Start date23 April 2020
Primary completion10 June 2020
Estimated completion15 June 2020
Sites1 location across Russia

Drugs / interventions tested

Conditions studied

Sponsor

SPP Pharmaclon Ltd. — full company profile →

Who can join

Adults 21 to 62, any sex, with COVID-19 Respiratory Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The main purpose of this study is to evaluate the effectiveness of the prophylactic use of Ingaron (INN: recombinant interferon gamma human, lyophilisate for solution for intranasal administration 100,000 IU) in the regimen of 3 drops in each nasal passage intranasally every other day for 10 days with a break of 7 days (2 10-day cycles) in volunteers.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Interferon gamma human recombinant (IFN-G)

Trials testing the same drug.

Other recruiting trials for COVID-19 Respiratory Infection

Currently open trials in the same condition.

Other SPP Pharmaclon Ltd. trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05386446.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing