Sym013

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m013 is a mixture of six humanized full length monoclonal antibodies targeting EGFR, HER2 and HER3 which is under development by Symphogen for the treatment of cancer (Company Pipeline Symphogen, FEB 22, 2014, View Source [SID:1234500115]).

(Press release, NBE Therapeutics, FEB 21, 2014, View Source;titolo=nbe-therapeutics-announces-validation-of-its-smac-technology-for-adc-development [SID:1234503548])

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Pending EC decision: Masiviera, masitinib, Opinion date: 23-Jan-2014

AB Science has requested a re-examination of Masiviera after the CHMP’s January 2014 opinion. Upon receipt of the grounds of the request, the CHMP will re-examine its opinion and issue a final recommendation (External Source EMA, AB Science, FEB 21, 2014, View Source [SID:1234500129]). On 23 January 2014, the Committee for Medicinal Products for Human Use (CHMP) adopted a negative opinion, recommending the refusal of the marketing authorisation for the medicinal product Masiviera, intended for the treatment of advanced inoperable pancreatic cancer.

Epizyme Announces Publication of Preclinical Data Demonstrating Clinical Candidate EPZ-6438 as Potent and Selective Inhibitor of EZH2 in Genetically Defined Non-Hodgkin Lymphoma

On February 21, 2014 Epizyme reported the publication of data from preclinical studies of the company’s clinical candidate EPZ-6438 (E7438), a potent and selective small-molecule inhibitor of EZH2, a histone methyltransferase (HMT). Oncogenic mutations in EZH2 occur in a subset of patients with non-Hodgkin lymphoma (NHL), implicating EZH2 as a therapeutic target in these patients (Press release Epizyme, FEB 21, 2014, View Source [SID:1234500113]). This research, published online and in the April issue of the journal Molecular Cancer Therapeutics, provides a preclinical description of EPZ-6438, which Epizyme is developing in partnership with Eisai for the treatment of EZH2 mutant-bearing NHL. The paper expands on data reported by the same authors in a poster presentation at the December 2012 American Society of Hematology (ASH) (Free ASH Whitepaper) annual meeting.

"This paper provides a comprehensive description of the preclinical characterization of EPZ-6438 that paved the way for this drug to enter human clinical trials in 2013," said Robert A. Copeland, Ph.D., executive vice president and chief scientific officer, Epizyme. "It is the first and only EZH2 inhibitor in clinical development to our knowledge. The work is illustrative of the ongoing discovery efforts at Epizyme that are fueling the clinical development of multiple drugs against the HMT target class."

Key results published in Molecular Cancer Therapeutics include:
* Detailed characterization of the correlation between EZH2 inhibition, methylation of the EZH2 target (H3K27), reversal of lymphomagenic gene expression and antiproliferative effects specific to EZH2 mutant-bearing NHL cell lines.
* Sustained tumor growth inhibition in animal models of EZH2 mutant-bearing NHL, including durable effects after drug dosing is discontinued.
* Development of an assay to assess methylation of H3K27 in tumor, bone marrow, peripheral blood mononuclear cells and other surrogate tissues.
* Determination of a quantitative PK/PD relationship using this assay.

The paper titled, "Selective Inhibition of EZH2 by EPZ-6438 Leads to Potent Antitumor Activity in EZH2 Mutant Non-Hodgkin Lymphoma," was authored by Sarah Knutson and colleagues at Epizyme and Eisai, and is available online here, View Source

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Novartis shows continued commitment in Japan with Lucentis approval in fourth Japanese indication, diabetic macular edema

pan (2014) as Lucentis has been approved by Japanese regulatory bodies for the treatment of patients with diabetic macular edema (DME) (Press release Novartis, FEB 20, 2014, View Source [SID:1234500112]).
Approval of Lucentis was based on results from the REVEAL trial, the first randomized clinical trial specifically designed to assess the efficacy and safety of Lucentis in Asian patients with visual impairment due to DME. In this Phase III trial, 396 patients from six countries, including Japan, were initially treated with monthly injections of 0.5 mg Lucentis, 0.5 mg Lucentis plus laser treatment or laser treatment alone for two months. Treatment was continued for twelve months if stable vision was not reached.
Efficacy and safety results from the REVEAL study were similar to other DME trials primarily conducted in Caucasians. At twelve months, REVEAL confirmed the superior efficacy of Lucentis with rapid and sustained visual acuity gains compared with laser therapy. Safety results showed that Lucentis was well tolerated in patients with DME both as monotherapy or when administered together with laser.

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