The Swiss drugmaker's deal with Australia-based Mesoblast secures
rights to develop, commercialize and manufacture Remestemcel-L for
treating acute respiratory distress syndrome (ARDS), including that
associated with COVID-19, for which the therapy is currently in
late-stage trials.
While the therapy has shown promise in COVID-19 patients -- -- in a
compassionate use programme in March in 12 patients, Remestemcel-L
was associated with an 83% survival rate --
Novartis wants the medicine for beyond the pandemic, too, to help
patients who in normal times also land in the hospital with ARDS and
often die.
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"It has the potential to be the first treatment for the most critically ill ARDS
patients, and it provides us with an opportunity to apply years of specialized
experience directly to the work of saving lives," Novartis's chief drug
developer, John Tsai, said on Friday.
Unlike Kymriah, Novartis's cancer cell therapy, Remestemcel-L does not have to
be tailored for each patient. Once the deal is closed, Novartis said it is
planning to help Mesoblast work on quality attributes of the therapy so it meets
U.S. Food and Drug Administration requirements necessary for late-stage trial
beyond COVID-19.
(Reporting by John Miller; Editing by Michael Shields)
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