Medivir presents new data at AACR showing significantly improved antitumor efficacy in non-clinical tumor models with fostrox in triple combination
Medivir AB (NASDAQ Stockholm: MVIR) announced a presentation at the AACR Annual Meeting on April 17, 2023, highlighting a poster titled 'A triple combination of fostrox (MIV-818) with immune checkpoint and kinase inhibition shows increased anti-tumor efficacy in vivo.' Fostrox, an orally administered prodrug for liver-targeted therapy, is undergoing a phase 1/2a clinical study for advanced hepatocellular carcinoma (HCC) in combination with Keytruda® and Lenvima®. Data suggests that this triple combination may enhance anti-tumor effects, showing increased tumor infiltration of CD8+ T cells and PD-L1 expression. Medivir aims to address the significant unmet medical need in HCC treatment, as current therapies often fail to provide satisfactory results for many patients.
- Presentation of promising data on fostrox's efficacy in combination therapies for HCC.
- Fostrox shows increased immune-mediated anti-tumor activity, indicating potential for better treatment outcomes.
- None.
Fostroxacitabine bralpamide (fostrox) is an orally administered liver-targeted prodrug currently undergoing a phase 1/2a clinical study in advanced hepatocellular carcinoma (HCC), in combination with Keytruda® (anti-PD1) or Lenvima® (kinase inhibitor) (NCT0341818). In previous studies, Fostrox has shown significantly increased anti-tumor effect in combination with both anti-PD1 and kinase inhibitors in non-clinical tumor models, which opens the door for a potentially further enhanced tumor effect with a triple combination.
The poster supports this potential as it exhibits that fostrox combined with both anti-PD1 and Lenvima® shows a synergistic anti-tumor effect in a non-clinical tumor model characterized by the same low, underlying DNA damage seen in patients with HCC. The poster also shows that fostrox induces increased tumor infiltration of CD8+ T cells as well as increased expression of PD-L1 and LAG-3, indicating increased immune-mediated antitumor activity. The results indicate a potential for triple combination of anti-PD1 and Lenvima® with fostrox in the treatment of HCC.
"Although existing combination treatments for HCC can prolong patients' lives, far from all patients respond to the treatment. In order for more patients to obtain a satisfactory effect on their treatment, new combination options with several different, additive mechanisms of action are needed. Fostrox, with its unique, liver-targeted activity, opens up for new combinations with three different approaches to effectively treat HCC," says
The poster will be available on
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E-mail: magnus.christensen@medivir.com
About fostrox
Fostrox is a pro-drug designed to selectively treat liver cancers and to minimize side effects. It has the potential to become the first liver-targeted and orally administered drug for patients with HCC and other forms of liver cancer. Fostrox has completed a phase 1b monotherapy study, and a combination study in HCC currently ongoing.
About primary liver cancer
Primary liver cancer is the third leading cause of cancer-related deaths worldwide and hepatocellular carcinoma (HCC) is the most common cancer that arises in the liver. Although existing therapies for advanced HCC can extend the lives of patients, treatment benefits are insufficient and death rates remain high. There are 42,000 patients diagnosed with primary liver cancer per year in the US and current five-year survival is
11 percent. HCC is a heterogeneous disease with diverse etiologies, and lacks defining mutations observed in many other cancers. This has contributed to the lack of success of molecularly targeted agents in HCC. The limited overall benefit, taken together with the poor overall prognosis for patients with intermediate and advanced HCC, results in a large unmet medical need.
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FAQ
What was presented about fostrox at the AACR Annual Meeting on April 17, 2023?
What is the current clinical status of fostrox for liver cancer treatment?
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