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Wired News – BeiGene Enrolled First Patient in Global Phase-2 Trial of Tislelizumab with Previously Treated HCC Patients

Stock Monitor: Madrigal Pharma Post Earnings Reporting

LONDON, UK / ACCESSWIRE / April 12, 2018 / Active-Investors.com has just released a free research report on BeiGene, Ltd (NASDAQ: BGNE). If you want access to this report all you need to do is sign up now by clicking the following link www.active-investors.com/registration-sg/?symbol=BGNE as the Company's latest news hit the wire. On April 10, 2018, the Company announced that the first patient was dosed in a global Phase-2 clinical trial of tislelizumab, an investigational anti-PD-1 antibody, in patients with previously treated advanced hepatocellular carcinoma (HCC or liver cancer). Register today and get access to over 1.000 Free Research Reports by joining our site below:

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Active-Investors.com is currently working on the research report for Madrigal Pharmaceuticals, Inc. (NASDAQ: MDGL), which also belongs to the Healthcare sector as the Company BeiGene. Do not miss out and become a member today for free to access this upcoming report at:

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Active-Investors.com is focused on giving you timely information and the inside line on companies that matter to you. This morning, BeiGene most recent news is on our radar and our team decided to put out a fantastic report on the company that is now available for free below:

www.active-investors.com/registration-sg/?symbol=BGNE

Phase-2 Multi-Center Trial Primary Endpoint is Overall Response Rate

The Phase-2, multi-center trial is designed to evaluate the efficacy and safety of tislelizumab in patients who were previously treated for unresectable HCC. The trail will enroll approximately 225 patients at 75 cancer centers internationally including Greater China (including Taiwan), the United States, and Europe. Patients will receive a 200mg dose every three weeks. The trial's primary endpoint is overall response rate (ORR), and secondary endpoints include duration of response (DOR), progression-free survival (PFS), disease control rate (DCR) and clinical benefit rate (CBR) and overall survival.

BeiGene Initiated Global Phase-3 Trial of Tislelizumab in Patients with Untreated HCC

In December 2017, the first patient was dosed in a global Phase-3 clinical trial of tislelizumab in patients with previously untreated advanced HCC. Tislelizumab was being evaluated in pivotal trials in four distinct indications. The Phase-3, open-label, multi-center, randomized trial was designed to compare the efficacy and safety of tislelizumab versus sorafenib as a potential first-line treatment in patients with unresectable HCC.

FDA Approved Drugs for Treatment of HCC

  • In April 2017, the US Food and Drug Administration (FDA) approved regorafenib (Stivarga) as a second-line treatment for patients with HCC who have previously received sorafenib.

  • In September 2017, the FDA granted accelerated approval to nivolumab (OPDIVO, Bristol-Myers Squibb Co.) for the treatment of HCC in patients who have been previously treated with sorafenib.

About Hepatocellular Carcinoma

HCC is the most common type of primary liver cancer in adults and is the most common cause of death in people with cirrhosis. It most commonly occurs in people with liver disease, particularly in people with chronic hepatitis B and C. Symptoms often do not appear in the early stages of cancer. Later, symptoms include weight loss, upper abdominal pain, or jaundice. Treatments may include surgery, transplant, freezing or heating the cancer cells, and chemotherapy.

About Tislelizumab

Tislelizumab (BGB-A317) is an investigational humanized monoclonal antibody that belongs to a class of immuno-oncology agents known as immune checkpoint inhibitors. It is designed to bind to PD-1, a cell surface receptor that plays an important role in downregulating the immune system by preventing the activation of T-cells. Tislelizumab has demonstrated high affinity and specificity for PD-1. Tislelizumab is being developed as a monotherapy and in combination with other therapies for the treatment of a broad array of both solid tumor and hematologic cancers. BeiGene and Celgene Corp. have a global strategic collaboration for tislelizumab for solid tumors outside of Asia (except Japan).

About BeiGene, Ltd

Founded in 2010 and headquartered in Cambridge, Massachusetts, BeiGene, Ltd is a global, commercial-stage, research-based biotechnology company focused on molecularly targeted and immuno-oncology cancer therapeutics. With a team of over 900 employees in China, the United States and Australia, the Company is advancing a pipeline consisting of novel oral small molecules and monoclonal antibodies for the treatment of cancer.

Stock Performance Snapshot

April 11, 2018 - At Wednesday's closing bell, BeiGene's stock declined 1.28%, ending the trading session at $171.82.

Volume traded for the day: 314.01 thousand shares.

Stock performance in the last month – up 11.35%; previous three-month period – up 71.25%; past twelve-month period – up 354.43%; and year-to-date - up 75.83%

After yesterday's close, BeiGene's market cap was at $9.06 billion.

The stock is part of the Healthcare sector, categorized under the Biotechnology industry.

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