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NCT04980534

Evaluation of the Effectiveness of Therapy for Patients With Covid-19 Using Food Supplements Viusid + Asbrip

Completed NA Last updated 13 April 2022
What this trial tests

NA trial testing Viusid and Asbrip in Covid19 in 80 participants. Completed in 15 September 2021.

Timeline
8 January 2021
Primary endpoint
30 June 2021
15 September 2021

Quick facts

Lead sponsorCatalysis SL
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment80
Start date8 January 2021
Primary completion30 June 2021
Estimated completion15 September 2021
Sites3 locations across Kazakhstan

Drugs / interventions tested

Conditions studied

Sponsor

Catalysis SL — full company profile →

Who can join

Adults 18 to 85, any sex, with Covid19 or COVID-19 Pneumonia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a two-arm, randomized, open label, monocenter, controlled study to evaluate the safety and efficacy of Viusid plus Asbrip in patients with mild and moderate symptoms of respiratory illness caused by Coronavirus 2019 infection.

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 Viusid and Asbrip

Trials testing the same drug.

Other recruiting trials for Covid19

Currently open trials in the same condition.

Other Catalysis SL trials

Trials by the same sponsor.

Verify against primary sources

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/NCT04980534.

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