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NCT04820751

Cyproheptadine in Severe COVID-19 : A Unblinded Randomized Trial

Status unknown Phase 3 Last updated 2 April 2021
What this trial tests

Phase 3 trial testing Cyproheptadine Hydrochloride 4 MG in Viral Pneumonia in 200 participants. Status unknown.

Timeline
10 April 2021
Primary endpoint
1 November 2021
1 January 2022

Quick facts

Lead sponsorCiusss de L'Est de l'Île de Montréal
PhasePhase 3
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment200
Start date10 April 2021
Primary completion1 November 2021
Estimated completion1 January 2022

Drugs / interventions tested

Conditions studied

Sponsor

Ciusss de L'Est de l'Île de Montréal — full company profile →

Who can join

Adults 18 to 99, any sex, with Viral Pneumonia or Serotonin Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This randomized controled open label clinical trial is to evaluate the effect of Cyproheptadine on the clinical course of patients presenting a severe SARS-COV 2 pneumonia.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Longitudinal gene expression analysis in COVID-19 sepsis highlights dynamic immune, cellular, and metabolic dysfunction in high severity patients.
    An AY, Baghela A, Zhang P, Blimkie TM, et al · · 2025 · PMID 41419557 · DOI 10.1038/s41598-025-32557-y

Verify or expand the search:

Other trials of Cyproheptadine Hydrochloride 4 MG

Trials testing the same drug.

Other recruiting trials for Viral Pneumonia

Currently open trials in the same condition.

Other Ciusss de L'Est de l'Île de Montréal 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/NCT04820751.

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