CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 190 enrolled
Drug / intervention
Selinexor +1 moredrug
Likely dose
Selinexor 20 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.

Search/NCT04349098
NCT04349098Phase 2Completed

A Phase 2 Randomized Single-Blind Study to Evaluate the Activity and Safety of Low Dose Oral Selinexor (KPT-330) in Patients With Severe COVID-19 Infection

Karyopharm Therapeutics Inc·interventional·Posted Apr 16, 2020·Updated Jan 20, 2023

In Brief

A Phase 2 clinical trial evaluating Selinexor and Placebo for Coronavirus Infection. Completed, enrolled 190 participants across 33 sites in 6 countries.

Detailed Summary

The main purpose of this study is to evaluate the activity of low dose oral selinexor (KPT-330) and to evaluate the clinical recovery, the viral load, length of hospitalization and the rate of morbidity and mortality in participants with severe COVID-19 compared to placebo. The study had 2 arms and evaluated selinexor 20 mg + standard of care (SoC) and placebo + SoC. As the treatment for COVID-19 is rapidly evolving, the SoC varied over time and across regions of the world.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustria, France, Israel, Spain, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
202120222023202420252026
First PostedApr 16, 2020
Enrollment StartApr 17, 2020
Primary CompletionOct 5, 2020
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 6.2 years ago

Interventions

Selinexordrug

Participants will receive 20 mg of selinexor.

Placeboother

Participants will receive 20 mg of placebo matched to selinexor.