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Medivir to present data for the combination of fostrox + Lenvima in HCC at ESMO GI

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Medivir AB announced that an abstract for the combination of fostrox + Lenvima in hepatocellular carcinoma (HCC) has been accepted for presentation at the European Society for Medical Oncology Gastrointestinal Cancers Congress. The abstract titled 'Liver pharmacodynamics in an open-label phase Ib/IIa study of fostrox in combination with lenvatinib in hepatocellular carcinoma' will be presented at the conference. The presentation will include pharmacodynamic data from patients in the ongoing clinical study, evaluating the impact on normal liver function and DNA damage in tumor cells vs healthy cells. It will also provide an update on efficacy endpoints as the study continues to mature. The poster will be available on Medivir's website after the presentation.

Medivir AB ha annunciato che un abstract riguardante la combinazione di fostrox e Lenvima per il trattamento del carcinoma epatocellulare (HCC) è stato accettato per la presentazione al Congresso di Oncologia Gastrointestinale della Società Europea di Oncologia Medica. L'abstract, intitolato 'Farmacodinamica epatica in uno studio aperto di fase Ib/IIa di fostrox in combinazione con lenvatinib nel carcinoma epatocellulare', sarà presentato alla conferenza. La presentazione includerà dati farmacodinamici dai pazienti nello studio clinico in corso, valutando l'impatto sulla funzione epatica normale e sui danni al DNA nelle cellule tumorali rispetto a quelle sane. Saranno inoltre forniti aggiornamenti sugli endpoint di efficacia man mano che lo studio procede. Il poster sarà disponibile sul sito web di Medivir dopo la presentazione.
Medivir AB anunció que un resumen sobre la combinación de fostrox y Lenvima para el carcinoma hepatocelular (HCC) ha sido aceptado para presentación en el Congreso de Cánceres Gastrointestinales de la Sociedad Europea de Oncología Médica. El resumen titulado 'Farmacodinámica hepática en un estudio abierto de fase Ib/IIa de fostrox en combinación con lenvatinib en carcinoma hepatocelular' será presentado en la conferencia. La presentación incluirá datos farmacodinámicos de pacientes en el estudio clínico en curso, evaluando el impacto en la función hepática normal y el daño al ADN en células tumorales versus células sanas. También proporcionará una actualización sobre los puntos finales de eficacia a medida que el estudio sigue madurando. El póster estará disponible en el sitio web de Medivir tras la presentación.
Medivir AB는 간세포암(HCC)치료를 위한 포스트록스와 렌비마의 조합에 대한 초록이 유럽 의학 종양학회 소화기암 콩그레스에서 발표될 것이라고 발표했습니다. '간세포암에서 포스트록스와 렌바티닙의 조합으로 진행된 개방형 1b/2a 단계 연구에서의 간약리학'이라는 제목의 초록이 회의에서 발표될 예정입니다. 발표는 진행 중인 임상 연구의 환자들로부터의 약리학적 데이터를 포함하여, 정상 간 기능과 종양세포와 건강세포의 DNA 손상에 미치는 영향을 평가할 것입니다. 또한 연구가 성숙함에 따라 효능 종료점에 대한 업데이트를 제공할 것입니다. 포스터는 발표 후 Medivir의 웹사이트에서 볼 수 있습니다.
Medivir AB a annoncé qu'un résumé sur la combinaison de fostrox et Lenvima pour le carcinome hépatocellulaire (CHC) a été accepté pour présentation au Congrès des cancers gastro-intestinaux de la Société Européenne d'Oncologie Médicale. Le résumé intitulé 'Pharmacodynamie hépatique dans une étude ouverte de phase Ib/IIa de fostrox en combinaison avec le lenvatinib dans le carcinome hépatocellulaire' sera présenté lors de la conférence. La présentation inclura des données pharmacodynamiques provenant de patients dans l'étude clinique en cours, évaluant l'impact sur la fonction hépatique normale et les dommages à l'ADN dans les cellules tumorales par rapport aux cellules saines. Elle fournira également une mise à jour sur les critères d'efficacité à mesure que l'étude continue de mûrir. L'affiche sera disponible sur le site web de Medivir après la présentation.
Medivir AB gab bekannt, dass ein Abstract zur Kombination von Fostrox und Lenvima bei hepatozellulärem Karzinom (HCC) zur Präsentation auf dem Kongress für gastrointestinale Krebserkrankungen der Europäischen Gesellschaft für medizinische Onkologie angenommen wurde. Der Abstract mit dem Titel 'Leberpharmakodynamik in einer offenen Phase-Ib/IIa-Studie von Fostrox in Kombination mit Lenvatinib bei hepatozellulärem Karzinom' wird auf der Konferenz präsentiert. Die Präsentation wird pharmakodynamische Daten von Patienten in der laufenden klinischen Studie umfassen, die die Auswirkungen auf die normale Leberfunktion und DNA-Schäden in Tumorzellen im Vergleich zu gesunden Zellen bewerten. Zudem werden Updates zu den Wirksamkeitsendpunkten bereitgestellt, da die Studie weiter fortschreitet. Das Poster wird nach der Präsentation auf der Website von Medivir verfügbar sein.
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STOCKHOLM, April 29, 2024 /PRNewswire/ -- Medivir AB (NASDAQ: MVIR) (STO: MVIR), a pharmaceutical company focused on developing innovative treatments for cancer in areas of high unmet medical need, announced today that an abstract for the combination of fostroxacitabine bralpamide (fostrox) + Lenvima® in hepatocellular carcinoma (HCC) has been accepted for presentation at the European Society for Medical Oncology (ESMO) Gastrointestinal (GI) Cancers Congress in June 26-29, 2024 in Munich.

The abstract, titled "Liver pharmacodynamics in an open-label phase Ib/IIa study of fostroxacitabine bralpamide (fostrox, MIV-818) in combination with lenvatinib in 2L/3L hepatocellular carcinoma" will be presented at the conference by Dr Hong Jae Chon, CHA Bundang Medical Center in Korea. Dr Chon is one of the investigators in the ongoing phase Ib/IIa study.

The presentation will include pharmacodynamic data from patients in the ongoing phase Ib/IIa clinical study with fostrox + Lenvima combination, evaluating the impact on normal liver function and DNA damage in tumor cells vs healthy cells. The presentation will also include an update on efficacy endpoints as the study has continued to mature and patients have been able to stay on treatment.

The poster will be available on Medivir's website after the presentation.

For additional information, please contact;

Magnus Christensen, CFO, Medivir AB
Telephone: +46 8 5468 3100
E-mail: magnus.christensen@medivir.com 

About fostrox

Fostrox is a type of smart chemotherapy that delivers the cell-killing compound selectively to the tumor while minimizing the harmful effect on normal cells. This is achieved by coupling an active chemotherapy (troxacitabine) with a prodrug tail. The prodrug design enables fostrox to be administered orally and travel directly to the liver where the active substance is released locally in the liver. With this unique mechanism, fostrox has the potential to become the first liver-targeted, orally administered drug that can help patients with various types of liver cancer. A phase 1b monotherapy study with fostrox has been completed and a phase 1b/2a combination study in HCC is 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 approximately 660,000 patients diagnosed with primary liver cancer per year globally and current five-year survival is less than 20 percent1). 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.

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 smart, targeted chemotherapy designed to selectively treat liver cancer cells 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.

1) Rumgay et al.,European Journal of Cancer 2022 vol.161, 108-118.

This information was brought to you by Cision http://news.cision.com

https://news.cision.com/medivir/r/medivir-to-present-data-for-the-combination-of-fostrox---lenvima-in-hcc-at-esmo-gi,c3969603

The following files are available for download:

https://mb.cision.com/Main/652/3969603/2766828.pdf

Press release (PDF)

 

Cision View original content:https://www.prnewswire.com/news-releases/medivir-to-present-data-for-the-combination-of-fostrox--lenvima-in-hcc-at-esmo-gi-302129837.html

SOURCE Medivir

FAQ

What combination was accepted for presentation at the ESMO GI Congress?

The combination of fostrox + Lenvima in hepatocellular carcinoma (HCC) was accepted for presentation.

When and where will the presentation take place?

The presentation will take place at the European Society for Medical Oncology (ESMO) Gastrointestinal (GI) Cancers Congress in June 26-29, 2024, in Munich.

Who will be presenting the abstract?

Dr. Hong Jae Chon, CHA Bundang Medical Center in Korea, will be presenting the abstract.

What will be included in the presentation?

The presentation will include pharmacodynamic data from patients in the ongoing clinical study, evaluating the impact on normal liver function and DNA damage in tumor cells vs healthy cells, as well as an update on efficacy endpoints.

Where will the poster be available after the presentation?

The poster will be available on Medivir's website after the presentation.

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