Our Vision

Improving life for cancer patients through transformative drugs

Why we do it

Cancer is the second leading cause of death and around 14 million new cases are diagnosed globally every year1. This number is expected to increase in the future driven by the world’s growing and aging population.

  1. WHO World cancer report 2014.

Cancer is more than 100 different diseases

Each type of cancer has a different characteristic and prognosis. Traditionally, cancers are named after the part of the body where it starts (for example lung, prostate and liver) and by the specific cells that have become cancerous (for example hepatocellular carcinoma, lymphomas and small cell lung cancer).

What is cancer?

A cancerous tumor occurs when cells divide in an uncontrolled manner. Genetic changes result in the cells stimulating both their own growth and the growth of blood vessels to and from the tumor.

When tumors grow, they can start invading surrounding tissues and also form subsidiary tumors (metastases). Furthermore, the tumor becomes resistant to the body’s immune responses, which would otherwise trigger the death of the cancer cells.

Medivir are developing anticancer drugs

to be delivered directly to the organ of the primary tumor in order to minimize systemic toxicity. MIV-818 target cancers of the liver and remetinostat (developed to treat early stage MF-CTCL) is only active on the skin.

Combining drug treatments

is an important tool to battle cancer. By combining several treatments targeting different mechanisms in the cell cycle, synergies can be reached that result in an improved efficacy.

Medivir is developing birinapant as a  combination treatment with Keytruda®  (Merck & Co). Keytruda® is an immuno-oncology agent that uses the body’s immune system to fight cancer.

Shorter lead times for development and launch

The FDA has introduced a number of processes to contribute to shorter lead times in drug development, such as “fast track designation”, “breakthrough therapy designation”, “accelerated approval” and “priority review”. Also at the European Medicines Agency EMA there are similar processes. Novel drug treatments can thus have the possibility to reach the cancer patients more rapidly.