Industry news

  • 23 May 2017

    Drama and diagnosis on soap opera set troubles cancer doctors, puts Incyte in hot seat

    Beth Snyder Bulik / FiercePharmaMarketing

    Soap operas often include medical mysteries and miracles, but a couple of real-life doctors are concerned about Incyte's connection to the latest drama on General Hospital.

  • 22 May 2017

    Pharma Must Embrace Its Social Media Role

    Dawn Lacallade / Pharmaceutical Executive

    Social media permeates virtually every aspect of a person’s digital life. Patients are using social media as a major source of information and an integral part of their healthcare research journey. It is therefore imperative that pharma companies be present on social media to provide full and balanced information to consumers.

  • 19 May 2017

    Health Executives See Tech Firms Like Alphabet Remaking Industry

    bSonali Basak and Ed Hammond / Bloomberg

    Health-care executives expect counterparts at tech companies like Alphabet Inc., Google’s parent company, to transform their industry over three to five years, according to a Lazard Ltd. survey.

  • 19 May 2017

    The top 15 generic drugmakers by 2016 revenue

    Eric Sagonowsky / FiercePharma

    Branded drugmakers weren't the only ones working through a tumultuous 2016. Generics companies faced pricing pressure, too. And while branded companies suffer pricing pain on costly cutting-edge therapies, generics outfits feel the pinch with already-thin margins, making pressure all the more agonizing.

  • 18 May 2017

    Behind the numbers: The pharmaceutical industry and global health

    Cristina Arnés / European Pharmaceutical Review

    The most indisputable of all facts on global health is that we’re living longer and healthier lives than ever, and in an era of continuous health improvement. What were once considered life-threatening diseases are now manageable conditions, and not just for patients, but for our health systems also.

  • 18 May 2017

    EMA Finds Patient Involvement Beneficial

    BioPharm International

    The European Medicines Agency (EMA) released a report on its pilot project to involve patients in the benefit-risk assessment of medicines at Committee for Medicinal Products for Human Use (CHMP) meetings. The agency concluded that patient involvement was beneficial and should continue.

  • 17 May 2017

    Syndax Announces Results from Phase 2 ENCORE 601 Trial of Entinostat in Combination with KEYTRUDA(R) (pembrolizumab) for the Treatment of Advanced Melanoma

    Syndax Announces Results from Phase 2 ENCORE 601 Trial of Entinostat in Combination with KEYTRUDA(R) (pembrolizumab) for the Treatment of Advanced Melanoma

    Syndax Pharmaceuticals, Inc. ("Syndax," the "Company" or "we") (Nasdaq:SNDX), a clinical stage biopharmaceutical company developing entinostat and SNDX-6352 in multiple cancer indications, today announced results from the melanoma cohort of the ongoing Phase 2 ENCORE 601 trial of entinostat in combination with KEYTRUDA® (pembrolizumab), Merck's anti-PD-1 (programmed death receptor-1) therapy, which will be presented at the American Society of Clinical Oncology (ASCO) Annual Meeting being held June 2-6, 2017 in Chicago, Illinois.

  • 17 May 2017

    New FDA Commissioner Gottlieb Reorganizing Inspection Staff

    Anna Edney / Bloomberg

    Federal inspectors who ensure the safety of the nation’s food and medical products will begin specializing in certain areas, as new Food and Drug Administration commissioner Scott Gottlieb enters his first full week at the agency.

  • 16 May 2017

    Syndax Pharmaceuticals Announces Advancement of ENCORE 601 in Non-Small Cell Lung Cancer Patients with Disease Progression on or After PD-1 Therapies

    Syndax Pharmaceuticals Announces Advancement of ENCORE 601 in Non-Small Cell Lung Cancer Patients with Disease Progression on or After PD-1 Therapies

    Syndax Pharmaceuticals, Inc. ("Syndax," the "Company" or "we") (Nasdaq:SNDX), a clinical stage biopharmaceutical company focused on developing entinostat and SNDX-6352 in multiple cancer indications, today reported that the ENCORE 601 non-small cell lung cancer (NSCLC) cohort enrolling patients with disease progression on or after PD-1 therapy (programmed death receptor-1 (PD-1) and/or programmed death ligand 1, (PD-L1)) has met the pre-specified objective response threshold to advance into the second stage of the Phase 2 trial, and will re-open enrollment immediately.

  • 16 May 2017

    Pharma and biotech rebound in annual trust study, but there's still room for improvement

    Beth Snyder Bulik / FiercePharmaMarketing

    When it comes to pharma, consumers still have trust issues. But the good news from Edelman’s 2017 Trust Barometer study is that things are improving. Fifty-one percent of Americans now say they trust the industry, a gain of 4% year over year. Biotech saw an even bigger jump of 12% to 62% this year. Both industries had dipped by 2% in the U.S. the year prior.

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