STOCKHOLM, Nov. 27,
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 finalized the development of an updated
formulation of fostrox, suitable for commercial manufacture. HCC is
a potentially life-threatening form of liver cancer and the third
leading cause of cancer-related death worldwide. The need for new
treatments is high and the development of an updated commercial
formulation is an additional step towards fostrox becoming a
treatment option for HCC patients.
The development efforts have been carried out by Quotient
Sciences, Medivir's partner for formulation development and
manufacture of drug product.
Fostrox is currently being evaluated in an ongoing phase
1b/2a study in combination with
Lenvima®, a tyrosine kinase inhibitor. It is an
open-label, multicenter study and includes patients with HCC for
whom current first- or second-line treatment has proven ineffective
or is not tolerable. It has the potential to provide HCC patients,
who have progressed on current first line standard of care, with an
alternative option where no other treatments are
approved.
With the study fully recruited and ~50% of patients still on
treatment, interim data indicates clinical benefit without
compromising safety, when fostrox is added to Lenvima in
second-line HCC. Based on these promising data, 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 formulation suitable for commercial manufacture is a critical
component in clinical studies with regulatory intent. With the
formulation development program successfully finalized, the next
step is to manufacture three different strengths of fostrox
together with placebo to ensure momentum in the fostrox development
program and enable a timely start of the planned phase 2b study.
- "With the plans to initiate a phase 2b study with registrational intent, it is
imperative that we use the formulation intended for commercial
launch in the study. We are very pleased with our collaboration
with Quotient Sciences on this updated, commercial formulation and
having the formulation at this stage enables us to keep maximum
momentum in the fostrox development program," 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. Birinapant, a SMAC mimetic, is
exclusively outlicensed to IGM Biosciences (Nasdaq: IGMS) to be
developed in combination with IGM-antibodies for the treatment of
solid tumors. Medivir's share (ticker: MVIR) is listed on Nasdaq
Stockholm's Small Cap list. www.medivir.com.
About Quotient Sciences
Quotient Sciences is a drug development and manufacturing
accelerator providing integrated programs and tailored services
across the entire development pathway. Cutting through silos across
a range of drug development capabilities, we save precious time and
money in getting drugs to patients. Everything we do for our
customers is driven by an unswerving belief that ideas need to
become solutions, and molecules need to become cures, fast. Because
humanity needs solutions, fast. For more information, please
visit quotientsciences.com.
The following files are available for download:
https://mb.cision.com/Main/652/3883046/2455065.pdf
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SOURCE Medivir