MESO just failed in COVID-19 Melbourne, Austral
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Posted On: 12/17/2020 6:27:16 PM
MESO just failed in COVID-19
Melbourne, Australia; December 18, and New York, USA; December 17, 2020:
Mesoblast
Limited (ASX:MSB; Nasdaq:MESO) today provided an update on the randomized controlled trial of
remestemcel-L in ventilator-dependent patients with moderate to severe acute respiratory distress
syndrome (ARDS) due to COVID-19 infection after the Data Safety Monitoring Board (DSMB)
performed a third interim analysis on the trial’s first 180 patients. The trial was powered to achieve a
primary endpoint of 43% reduction in mortality at 30 days for treatment with remestemcel-L on top of
maximal care in a trial of 300 patients. This projected mortality reduction was based on pilot data
observed during the initial stages of the pandemic when control mortality rates were exceedingly high
and prior to new evolving treatment regimens that have reduced disease mortality in ventilated
patients. The DSMB reported that there were no safety concerns and noted that the trial is not likely
to meet the 30-day mortality reduction endpoint at the planned 300 patient enrolment. The DSMB
recommended that the trial complete with the currently enrolled 223 patients, and that all be
followed-up as planned.
Notably, the trial has not yet accrued data on the secondary endpoints, which include days alive off
mechanical ventilation at 60 days post randomization, overall survival, days in intensive care, duration
of hospitalization, and cardiac, neurological, and pulmonary organ damage. Additionally, measures of
circulating cytokines and inflammatory markers will be evaluated. None of these were included in the
interim analysis. As such, the trial will evaluate all 223 enrolled patients through 60 days of follow-up
to study potential treatment effects on these outcomes. Mesoblast and Novartis will both analyse
these results to identify meaningful clinical outcomes that may guide decisions on the development
program for remestemcel-L in non-COVID ARDS.
During the course of the trial, as the pandemic has evolved, numerous changes in the treatment
regimens for COVID-19 patients occurred, including both prior to and while on mechanical ventilation
that may have an effect on the mortality endpoint in the trial. These include extended management of
patients prior to ventilator support, and use of experimental therapies such as dexamethasone, anti-
virals, and re-purposed immunomodulatory agents. All of these may have changed the natural course
of ventilated patients and reduced overall mortality rates during the trial compared to the early stages
of the pandemic.
Mesoblast entered into a license and collaboration agreement with Novartis on November 20, 2020 for
the development, manufacture and commercialization of remestemcel-L, with an initial focus on the
treatment of ARDS, including that associated with COVID-19, and other indications. The closing of the
agreement is subject to the expiration or termination of the waiting period under the Hart-Scott-
Rodino Antitrust Improvements Act and certain other conditions.
About Remestemcel-L
Remestemcel-L is an investigational therapy comprising culture-expanded
Melbourne, Australia; December 18, and New York, USA; December 17, 2020:
Mesoblast
Limited (ASX:MSB; Nasdaq:MESO) today provided an update on the randomized controlled trial of
remestemcel-L in ventilator-dependent patients with moderate to severe acute respiratory distress
syndrome (ARDS) due to COVID-19 infection after the Data Safety Monitoring Board (DSMB)
performed a third interim analysis on the trial’s first 180 patients. The trial was powered to achieve a
primary endpoint of 43% reduction in mortality at 30 days for treatment with remestemcel-L on top of
maximal care in a trial of 300 patients. This projected mortality reduction was based on pilot data
observed during the initial stages of the pandemic when control mortality rates were exceedingly high
and prior to new evolving treatment regimens that have reduced disease mortality in ventilated
patients. The DSMB reported that there were no safety concerns and noted that the trial is not likely
to meet the 30-day mortality reduction endpoint at the planned 300 patient enrolment. The DSMB
recommended that the trial complete with the currently enrolled 223 patients, and that all be
followed-up as planned.
Notably, the trial has not yet accrued data on the secondary endpoints, which include days alive off
mechanical ventilation at 60 days post randomization, overall survival, days in intensive care, duration
of hospitalization, and cardiac, neurological, and pulmonary organ damage. Additionally, measures of
circulating cytokines and inflammatory markers will be evaluated. None of these were included in the
interim analysis. As such, the trial will evaluate all 223 enrolled patients through 60 days of follow-up
to study potential treatment effects on these outcomes. Mesoblast and Novartis will both analyse
these results to identify meaningful clinical outcomes that may guide decisions on the development
program for remestemcel-L in non-COVID ARDS.
During the course of the trial, as the pandemic has evolved, numerous changes in the treatment
regimens for COVID-19 patients occurred, including both prior to and while on mechanical ventilation
that may have an effect on the mortality endpoint in the trial. These include extended management of
patients prior to ventilator support, and use of experimental therapies such as dexamethasone, anti-
virals, and re-purposed immunomodulatory agents. All of these may have changed the natural course
of ventilated patients and reduced overall mortality rates during the trial compared to the early stages
of the pandemic.
Mesoblast entered into a license and collaboration agreement with Novartis on November 20, 2020 for
the development, manufacture and commercialization of remestemcel-L, with an initial focus on the
treatment of ARDS, including that associated with COVID-19, and other indications. The closing of the
agreement is subject to the expiration or termination of the waiting period under the Hart-Scott-
Rodino Antitrust Improvements Act and certain other conditions.
About Remestemcel-L
Remestemcel-L is an investigational therapy comprising culture-expanded
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