RedHill’s opaganib fails to meet Phase II/III Covid-19 trial primary goal
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RedHill’s opaganib fails to meet Phase II/III Covid-19 trial primary goal

15 Sep 2021 (Last Updated September 15th, 2021 12:22)

In the trial, opaganib was demonstrated to be tolerable with similar adverse events observed in both study groups.

RedHill’s opaganib fails to meet Phase II/III Covid-19 trial primary goal
Data indicate that opaganib offered improved benefit in a subset of Covid-19 patients needing less oxygen. Credit: Fusion Medical Animation / Unsplash.

RedHill Biopharma has reported initial top-line results where its investigational drug, opaganib (ABC294640), failed to meet the primary goal in the global Phase II/III clinical trial in severe Covid-19 pneumonia patients in the hospital.

A new chemical entity, opaganib selectively hinders sphingosine kinase-2 (SK2), a vital enzyme created in human cells that may be used by the virus to aid in its replication.

The drug possesses an anti-inflammatory and antiviral mechanism of action that works on the Covid-19’s viral cause an inflammatory effect.

Opaganib, which is host-targeted, is anticipated to be efficient against emerging viral variants, with already established robust hindering against variants of concern, such as Delta.

The multi-centre, randomised, double-blind, parallel-arm, placebo-controlled Phase II/III trial enrolled 475 subjects with severe Covid-19 pneumonia needing hospitalisation and supplemental oxygen.

Participants were categorised in a 1:1 ratio to be given either opaganib or placebo, along with standard-of-care treatment.

The proportion of subjects breathing room air without oxygen support by day 14 was the trial’s primary goal.

According to preliminary top-line results, analysis of efficacy demonstrated trends favouring the opaganib group as against placebo, across various endpoints, but statistical significance was not met.

Similar trends were observed even for the primary goal without attaining statistical significance, Redhill noted.

Under the safety data, opaganib was found to be tolerable with balanced adverse events between the trial groups.

These data, along with initial analysis indicate the improved benefit in a subset of patients needing less oxygen and could back the potential use of opaganib in earlier disease stages.

Furthermore, the data is consistent with the already reported results from the Phase II trial in the US and the previously noted antiviral activity of the drug.

Assessment of the top-line data is underway with the company planning to share the results with various regulatory agencies to decide on further steps.

RedHill Biopharma CEO Dror Ben Asher said: “While we are disappointed with the data not reaching statistical significance, we do see a trend that needs to be investigated that opaganib may provide benefit to patients earlier in the course of the disease.

“This correlates with what we know about opaganib’s strong antiviral mechanism and effect against variants, as well as its mechanism of action and previously announced results from the Phase II US study with opaganib.”

The latest development comes after RedHill announced plans to commence the Phase II/III clinical trial of its new drug candidate, RHB-107 (upamostat) to treat non-hospitalised patients with symptomatic Covid-19 in South Africa.