Amgen To Present At The Goldman Sachs 40th Annual Global Healthcare Conference

On June 7, 2019 Amgen (NASDAQ:AMGN) reported that it will present at the Goldman Sachs 40th Annual Global Healthcare Conference at 11:20 a.m. PT on Wednesday, June 12, 2019, in Rancho Palos Verdes, Calif. David M. Reese, M.D., executive vice president of Research and Development at Amgen, will present at the conference (Press release, Amgen, JUN 7, 2019, View Source;p=RssLanding&cat=news&id=2400957 [SID1234536952]). Live audio of the presentation can be accessed from the Events Calendar on Amgen’s website, www.amgen.com, under Investors. A replay of the webcast will also be available on Amgen’s website for at least 90 days following the event.

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Surface Oncology to Participate in 40th Annual Goldman Sachs Global Healthcare Conference

On June 7, 2019 Surface Oncology (NASDAQ:SURF), a clinical-stage immuno-oncology company developing next-generation immunotherapies that target the tumor microenvironment, reported that Jeff Goater, chief executive officer, will participate in the Goldman Sachs 40th Annual Global Healthcare Conference on Wednesday, June 12, 2019 at the Terranea Resort in Rancho Palos Verdes, CA (Press release, Surface Oncology, JUN 7, 2019, View Source [SID1234536951]).

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The corporate presentation will be accessible by visiting the Events and Presentations page of the website at View Source

British Company Behind Groundbreaking Breast Cancer Treatment

On June 7, 2019 Astex Pharmaceuticals reported A new set of statistically significant overall survival (OS) data unveiled at the 2019 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting (Abstract# LBA1008), and published in The New England Journal of Medicine, are being heralded as a major breakthrough forpre- and perimenopausal women with hormone receptor positive, human epidermal growth factor receptor-2 negative (HR+/HER2-) advanced or metastatic breast cancerpremenopausal women with advanced breast cancer (Press release, Astex Pharmaceuticals, JUN 7, 2019, View Source [SID1234536950]).

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Kisqali was discovered and developed by the Novartis Institutes for Biomedical Research (NIBR) under a research collaboration entered into with Astex in 2005. Kisqali is a CDK4/6 inhibitor that slows the progression of cancer by inhibiting two proteins (CDK4 & CDK6) which, when over-activated, can enable cancer cells to grow and divide quickly.

Successful results from the phase III MONALEESA-7 clinical trial resulted in Kisqali receiving marketing approval in the US and EU in 2018 in combination with an endocrine-based therapy for pre- and perimenopausal women with (HR+/HER2-) locally advanced or metastatic breast cancer in combination with an aromatase inhibitor.

The UK’s National Institute for Health and Care Excellence (NICE) recommended Kisqali as a cost-effective treatment option for postmenopausal women within England and Wales with advanced breast cancer in November 2017. Advanced breast cancer in premenopausal women is the leading cause of cancer death in women 20-59 years old [1],[2].

Kisqali is the only CDK4/6 inhibitor to show superior overall survival in a clinical trial (alt. "v. placebo") in advanced breast cancer (HR=0.712; p=0.00973)[3]. In its announcement at ASCO (Free ASCO Whitepaper), Novartis noted that the new data from its MONALEESA-7 trial showed that after a median of 42 months follow-up, survival rate for women was 70.2% for women who received Kisqali combination therapy compared to 46.0% for women who received endocrine therapy alone. The breakthrough data has been widely reported in the world’s press.

Harren Jhoti Ph.D., President and CEO of Astex, UK, said, "It’s fantastic to see such a significant advance in cancer treatment. Ultimately as life science entrepreneurs, our goal is to improve lives through the discovery of new therapies. Kisqali was the first new cancer drug discovered and developed from our collaboration with Novartis to reach marketing approval and was a milestone for the company in 2017. These new data are a real milestone for patients."
The paper,Overall Survival with Ribociclib plus Endocrine Therapy in Breast Cancer, was a published in The New England Journal of Medicinetoday and is available online.

See the discovery journey for Kisqali, here: View Source

AbbVie to Present at the Goldman Sachs Global Healthcare Conference

On June 7, 2019 AbbVie (NYSE: ABBV), a research-based global biopharmaceutical company, reported that it will participate in the Goldman Sachs 40th Annual Global Healthcare Conference on Wednesday, June 12, 2019 (Press release, AbbVie, JUN 7, 2019, View Source [SID1234536949]). Michael Severino, vice chairman and president, will present at 10:00 a.m. Central time.

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A live audio webcast of the presentation will be accessible through AbbVie’s Investor Relations website at investors.abbvie.com. An archived edition of the session will be available later that day.

Otsuka and Taiho Announce that Taiho Will Commercialize Two of Astex Pharmaceuticals’ Drug Candidates in North America

On June 7, 2019 Otsuka Pharmaceutical Co., Ltd. (Otsuka) and Taiho Pharmaceutical Co., Ltd. reported that commercialization rights in the U.S. and Canada for anti-cancer drug candidates guadecitabine and ASTX727 will be transferred to Taiho Oncology, Inc. and Taiho Pharma Canada, Inc., respectively, from Astex Pharmaceuticals, an Otsuka subsidiary (Press release, Taiho, JUN 7, 2019, View Source [SID1234536942]). Otsuka and Taiho are both part of the Otsuka group of companies.

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Taiho Pharmaceutical presently markets its antineoplatic agent LONSURF (trifluridine and tipiracil) in the U.S. and Canada, respectively, through subsidiaries Taiho Oncology and Taiho Pharma Canada. Astex will remain responsible for development of its two promising, late-stage-development candidates, guadecitabine and ASTX727.

Otsuka Pharmaceutical and Taiho Pharmaceutical aim to maximize their business impact and value by bringing together assets from across the Otsuka group of companies, including their respective strengths and experiences in the oncologic, psychiatric, neurologic, cardiovascular and renal fields.

Astex’s development-stage drug candidates for which North American commercialization rights will be transferred include: Guadecitabine Acute myeloid leukemia(AML) Phase 3 Myelodysplastic syndrome(MDS) Phase 3 Ovarian cancer Phase 2 A next-generation, low-molecular-weight DNA methylation inhibitor that is designed to allow the active metabolite decitabine to work longer in the body and thereby efficiently reach tissues such as the bone marrow. Therapeutic effects on patients with MDS and AML are hypothesized to occur through restoration of the function of inactivated tumor suppressor genes in cancer cells, thereby suppressing cancer formation and growth.

ASTX727 Myelodysplastic syndrome(MDS) Phase 3 The first-ever, fixed-dose-combination, oral DNA methylation inhibitor that combines the metabolic enzyme inhibitor cedazuridine with decitabine, the active ingredient of the DNA methylation inhibitor Dacogen. Preliminary results of phase 3 trials in patients with MDS indicated that the plasma drug concentration-time curve (AUC) and pharmacodynamics, safety, and tolerability were equivalent to those of Dacogen injections.