At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 22 enrolled
Drug / intervention
Thymic peptidesbiological
Likely dose
Thymic peptides 250 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Single-arm, Open-Label, Phase II Clinical Study to Evaluate the Safety and Efficacy of Thymic Peptides in the Treatment of Hospitalized COVID-19 Patients in Honduras
In Brief
A Phase 2 clinical trial evaluating Thymic peptides for COVID-19. Completed, enrolled 22 participants across 1 site.
Detailed Summary
This is a single-arm, open-label, phase II clinical study to evaluate the safety and efficacy of thymic peptides in the treatment of hospitalized COVID-19 patients in Honduras.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCOVID-19
CountriesHonduras
CollaboratorsPontificia Universidad Catolica de Chile
Timeline
Phase 2CompletedFinished
202120222023202420252026
Enrollment StartFeb 2021
First PostedFeb 2021
Primary CompletionMay 2021
TodayJul 2026
First PostedFeb 25, 2021
Enrollment StartFeb 10, 2021
Primary CompletionMay 14, 2021
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 5.4 years ago
Interventions
Thymic peptidesbiological
250 mg oral daily dose of lyophilized thymic peptides dissolved in 50 mL of water, administered with an empty stomach.