10-Q – Quarterly report [Sections 13 or 15(d)]

Gilead Sciences has filed a 10-Q – Quarterly report [Sections 13 or 15(d)] with the U.S. Securities and Exchange Commission (Filing 10-Q , Gilead Sciences, AUG 4, 2014, View Source [SID1234500680]).

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10-Q – Quarterly report [Sections 13 or 15(d)]

Isis Pharmaceuticals has filed a 10-Q – Quarterly report [Sections 13 or 15(d)] with the U.S. Securities and Exchange Commission (Filing 10-Q , Isis Pharmaceuticals, AUG 4, 2014, View Source [SID1234500683]).

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Regen BioPharma Provides Update on dCellVax Breast Cancer Immunotherapy

It successfully achieved silencing of the IDO gene in human dendritic cells (Press release ReGen Therapeutics, AUG 1, 2014, View Source [SID:1234500857]). This is the first experiments in which human cells were utilized in a manner similar to which will be filed with the US FDA.

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EMA GRANTS EISAI’S ANTICANCER AGENT LENVATINIB REQUEST FOR ACCELERATED ASSESSMENT

On July 31, 2014 Eisai reported that its U.K. subsidiary Eisai Europe Ltd. has been granted an accelerated review by the European Medicines Agency (EMA) for its in-house developed anticancer agent lenvatinib mesylate ("lenvatinib") in the treatment of radioiodine-refractory differentiated thyroid cancer (Press release Eisai, JUL 30, 2014, View Source [SID:1234500704]).

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The EMA’s accelerated review procedure is granted for new medicines that are expected to be of major public health interest, particularly from the viewpoint of therapeutic innovation. Currently, Eisai is planning to submit applications for marketing authorization in Europe and the U.S. in the second quarter of fiscal 2014. In addition, the first application for marketing authorization of lenvatinib in the world was submitted in Japan in June 2014.

Lenvatinib is an oral multiple receptor tyrosine kinase (RTK) inhibitor with a novel binding mode that selectively inhibits the kinase activities of vascular endothelial growth factor receptors (VEGFR), in addition to other proangiogenic and oncogenic pathway-related RTKs including fibroblast growth factor receptors (FGFR), the platelet-derived growth factor (PDGF) receptor PDGFRα, KIT and RET that are involved in tumor proliferation. This potentially makes lenvatinib a first-in-class treatment, especially given that it simultaneously inhibits the kinase activities of FGFR as well as VEGFR. It was granted Orphan Drug Designation for thyroid cancer by the health authorities in Japan, Europe and the U.S.

In Europe alone, over 50,000 cases of thyroid cancer were diagnosed in 2012. Although treatment is possible for most types of thyroid cancer, there remains an unmet need for treatment options once the disease has progressed.

Eisai is committed to exploring the potential clinical benefits of lenvatinib in order to further contribute to patients with cancer and their families.

ImmuNext Extends and Expands Collaboration with Janssen to Develop Novel Immunotherapies for the Treatment of Cancer

On July 29, 2014 ImmuNext reported that it has extended and expanded its collaboration with Janssen Biotech, Inc., focused on the development of novel therapeutics that modulate the immune system for the treatment of cancer (Press release ImmuNext, JUL 29, 2014, http://immunext.com/news.php [SID:1234500870]).

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ImmuNext has extended its collaborative effort with Janssen to carry out research and development of cancer therapeutics that antagonize the VISTA signaling pathway. VISTA is a novel negative checkpoint regulator. Janssen will be responsible for clinical development and commercialization of all products under the agreement.

In addition, ImmuNext has expanded the collaboration with Janssen to now include discovery of new targets for modulation of the immune system for the treatment of cancer.

"We have made great progress in our collaboration with Janssen, a global leader in the field of oncology, and we look forward to continuing our collaborative efforts to develop innovative immunotherapies to improve the lives of cancer patients," commented David DeLucia, ImmuNext’s chief executive officer.