STOCKHOLM, Dec. 13,
2023 /PRNewswire/ -- Medivir AB (Nasdaq Stockholm:
MVIR), a pharmaceutical company focused on developing innovative
treatments for cancer in areas of high unmet medical need,
announced today that it has signed an agreement with Lonza for the
manufacture of a new GMP campaign of fostrox drug substance for the
planned phase 2b to enable study drug
availability end of 2024 and ensure maximum momentum in the fostrox
development program.
In addition, Lonza, Medivir's partner for process development
and manufacture of drug substance, has developed a process suitable
for commercial manufacture of fostrox drug substance with plans
underway for the final optimization, qualification and validation
activities needed to support an accelerated approval after the
planned phase 2b study. Lonza will
also provide expert regulatory services to Medivir.
Based on promising clinical data for fostrox + Lenvima in the
ongoing phase 1b/2a study in second
line HCC, together with the lack of approved medical treatments
after tumor progression on first line standard of care, the company
has communicated the plan to initiate phase 2b study with accelerated approval intent. A GMP
campaign of fostrox, produced with an updated process suitable for
commercial manufacture, is critical to enable study start of the
planned study.
"This is another important step in our efforts to ensure speed
and momentum in the fostrox development program. It has the
potential to become the first, approved treatment option for
patients that have progressed on current first line standard of
care and it is imperative that we move ahead with as much speed as
possible. We are very pleased with our collaboration with Lonza to
ensure continued momentum.", says Jens
Lindberg, CEO at Medivir.
For additional information, please contact;
Magnus Christensen, CFO, Medivir
AB
Telephone: +46 8 5468 3100
E-mail: magnus.christensen@medivir.com
About Medivir
Medivir develops innovative drugs with a focus on cancer where
the unmet medical needs are high. The drug candidates are directed
toward indication areas where available therapies are limited or
missing and there are great opportunities to offer significant
improvements to patients. Medivir is focusing on the development of
fostroxacitabine bralpamide (fostrox), a pro-drug designed to
selectively treat liver cancer and to minimize side effects.
Collaborations and partnerships are important parts of Medivir's
business model, and the drug development is conducted either by
Medivir or in partnership. Medivir's share (ticker: MVIR) is listed
on Nasdaq Stockholm's Small Cap list. www.medivir.com.
The following files are available for download:
https://mb.cision.com/Main/652/3892840/2490627.pdf
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SOURCE Medivir