医療従事者の為の最新医療ニュースや様々な情報・ツールを提供する医療総合サイト

Apogenix Provides Update on Clinical Development of Asunercept

2018年05月23日 PM07:22
このエントリーをはてなブックマークに追加


 

HEIDELBERG, Germany

Apogenix AG, a biopharmaceutical company developing next-generation immuno-oncology therapeutics, today provides an update on the clinical development and approval strategy of its lead drug candidate asunercept.

In May 2017, asunercept received PRIME (PRIority MEdicines) designation by the European Medicines Agency (EMA) for the treatment of glioblastoma. In November 2017, Apogenix had the kick-off meeting for the PRIME procedure with the EMA and presented its plan to make asunercept available to patients suffering from recurrent glioblastoma as fast as possible. The company prepared an update of overall survival data from its phase II trial with asunercept in recurrent glioblastoma for the kick-off meeting. This update revealed that the five-year overall survival rate for patients treated with asunercept was 7 percent. There were no patients treated with radiotherapy alone who survived five years.

As an outcome of the kick-off meeting, the EMA invited Apogenix to discuss the entire asunercept data set in a pre-assessment meeting with the agency. Apogenix is working closely with the EMA to accelerate the approval process of asunercept and intends to submit a marketing authorization application (MAA) for conditional approval of asunercept in recurrent glioblastoma by the end of 2019.

Chinese licensing partner CANbridge recently announced the approval of an investigational new drug (IND) application by the China Food and Drug Administration for a pivotal phase II/III clinical trial with asunercept (CAN008) to treat patients with recurrent glioblastoma in China. The randomized, double-blind, placebo-controlled, multicenter phase II/III trial will evaluate the efficacy and safety of weekly re-radiation therapy in combination with asunercept. The study’s primary endpoint is overall survival. CANbridge anticipates dosing the first patient later this year.

“We are excited about the support that Apogenix is receiving from the EMA in the PRIME process,” said Harald Fricke, M.D., Chief Medical Officer of Apogenix. “We are also very pleased with the progress our Chinese licensing partner CANbridge is making in the clinical development of asunercept in China. The clinical and safety data from CANbridge’s phase II/III trial with asunercept in China and our phase II trial in Europe will help both sides ensure that patients suffering from recurrent glioblastoma can benefit from this novel treatment option as fast as possible.”

About Asunercept
Apogenix’ lead immuno-oncology candidate asunercept is a fully human fusion protein that consists of the extracellular domain of the CD95 receptor and the Fc domain of an IgG1 antibody. It is being developed for the treatment of solid tumors and malignant hematological diseases. Asunercept was granted orphan drug designation for the treatment of glioblastoma and myelodysplastic syndromes (MDS) in both the EU and the US. In 2017, asunercept received PRIME (PRIority MEdicines) designation by the European Medicines Agency (EMA) for the treatment of glioblastoma.

About Apogenix
Apogenix is a private company developing innovative immuno-oncology therapeutics for the treatment of cancer and other malignant diseases. The Heidelberg, Germany-based company has built a promising pipeline of immuno-oncology drug candidates that target different tumor necrosis factor (TNF) superfamily-dependent signaling pathways, thereby restoring the immune response against tumors. Checkpoint inhibitor asunercept, the company’s lead immuno-oncology candidate, is in late-stage clinical development. Based on its proprietary technology platform for the construction of novel hexavalent TNF superfamily receptor agonists (HERA), Apogenix develops CD40, CD27, GITR, HVEM, 4-1BB, and OX40 receptor agonists for cancer immunotherapy.

In 2015, Apogenix entered into an exclusive licensing agreement with CANbridge Life Sciences for the development and commercialization of asunercept for the treatment of glioblastoma in China, Macao, Hong Kong, and Taiwan. CANbridge has received approval by the China Food and Drug Administration for a pivotal phase II/III trial with asunercept (CAN008) in glioblastoma in China. The HERA-TRAIL receptor agonist program was out-licensed to AbbVie in 2014. In 2017, AbbVie initiated a phase I trial with this HERA-TRAIL receptor agonist (ABBV-621) in 92 patients suffering from solid tumors, non-Hodgkins’s lymphoma, or acute myeloid leukemia.

View source version on businesswire.com: https://www.businesswire.com/news/home/20180523005609/en/

CONTACT

Apogenix AG
Thomas Höger, Ph.D.
CEO
Phone: +49
6221 58608-0
E-Mail: contact@apogenix.com
Web:
www.apogenix.com
or
Media
Contact

MC Services AG
Katja Arnold / Andreas
Jungfer
Phone: +49 89 210228-0
E-Mail: apogenix@mc-services.eu

Related Posts Plugin for WordPress, Blogger...
 

同じカテゴリーの記事 

  • CANbridge Life Sciences Receives Approval to Commence CAN017 Ib/III Trial in Esophageal Squamous Cell Cancer (ESCC) In China
  • AVEO Announces Acceptance of CANbridge Investigational New Drug Application for CAN017 (AV-203) Trial in Esophageal Squamous Cell Cancer (ESCC) in China
  • STAAR Surgical and Shinjuku LASIK Clinic in Japan Announce Strategic Cooperation Agreement
  • 新研究调查诊断性多通道睡眠检查之前采用Masimo SET®脉搏氧饱和度仪居家监测筛查唐氏综合征患儿罹患阻塞性睡眠呼吸暂停的风险
  • ダウン症候群の小児を対象とする睡眠時障害診断のマルチチャンネル研究に先立つ閉塞性睡眠時無呼吸症リスクのスクリーニングとしてMasimo SET®パルスオキシメトリーを使用するホームモニタリングの有用性を検討する新研究