Marketing: Page 48


  • Kite first to file for CAR-T approval in Europe

    In the U.S., however, Novartis looks set to secure the first approval for a CAR-T therapy, winning the unanimous support of a FDA advisory panel in July. 

    By Suzanne Elvidge • Aug. 2, 2017
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    Dollar Photo Club
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    Idhifa approval furthers Celgene's diversification goals

    Revlimid continues to make up 60% of Celgene's revenues, but a new product for acute myeloid leukemia could help spread the wealth.

    By Aug. 1, 2017
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    Brian Tucker / BioPharma Dive/BioPharma Dive
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    Trendline

    Commercialization

    New drugs for obesity and Alzheimer’s look set to become blockbusters, reshaping pharma marketing strategies just as many current top-sellers near looming patent cliffs.

    By BioPharma Dive staff
  • Puma's early Nerlynx launch raises doubts of a takeover

    The company's decision to commercialize its breast cancer drug dampens the prospect of a near-term acquisition, according to a recent analyst report. 

    By Aug. 1, 2017
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    MicroMass
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    Sponsored by MicroMass Communications, Inc.

    Instead of being patient centered, try being patient informed

    To be successful, a brand must go beyond persuasive product messages and work to support the whole patient, not just their clinical needs. 

    By Meredith Terry, Senior Behaviorist • Aug. 1, 2017
  • Vertex wins new Kalydeco approval, ups sales forecast

    A label expansion will increase the patient population treatable by Vertex's older cystic fibrosis drug, strengthening the biotech's position.

    By Ned Pagliarulo • Aug. 1, 2017
  • Express Scripts shuts out 64 branded drugs from 2018 formulary

    Among the drugs excluded from the PBM's preferred list were Amgen's Neupogen, Eli Lilly's Forteo and Synergy Pharmaceuticals' newly approved Trulance.

    By Ned Pagliarulo • July 31, 2017
  • AbbVie confident in strategy as Humira mints money

    Despite growing competitive threats in immunology, AbbVie believes it can maintain its leadership position.

    By Ned Pagliarulo • July 28, 2017
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    Tesaro
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    Tesaro lands licensing, supply agreements for Zejula

    Two separate deals have Takeda handing over $100 million upfront for rights to the cancer med and STA Pharmaceutical providing the materials to make it.

    By July 27, 2017
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    FDA
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    GSK gets go-ahead for new Benlysta formulation

    Approval brings the first self-injectable treatment for the most common form of lupus to market, according to the British drugmaker.

    By July 26, 2017
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    Getty Images
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    Merck undercuts Pfizer on Remicade biosimilar price

    Looking to steal share, Merck priced its biosimilar version at a 35% discount to Remicade's list price, upping the threat faced by J&J's blockbuster biologic.

    By Ned Pagliarulo • July 26, 2017
  • AbbVie faces $150M in damages in AndroGel trial

    The Illinois drugmaker will have to pay up for fraudulent representation of the testosterone treatment and faces further damages as class action suits progress.

    By Suzanne Elvidge • July 26, 2017
  • Celgene pays $280M to make fraud allegations go away

    The big biotech admitted no wrongdoing, but settled the lawsuit in hopes of putting the off-label promotion matter in the past and off its balance sheet.

    By July 26, 2017
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    Biogen
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    Spinraza launch set for blockbuster trajectory

    Biogen surprised the markets with stronger-than-expected earnings for its rare disease drug. But can those sales last?

    By Lisa LaMotta • July 25, 2017
  • 5 orphan drugs receive EMA thumbs-up

    Pfizer and Merck KGaA's Bavencio and Novartis' Rydapt were among the 11 drugs recommended for approval during the Committee for Medicinal Products for Human Use's July meeting.

    By July 21, 2017
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    FDA
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    May day: Amgen, Novartis lock down lead for CGRP

    The FDA gave a May 17 target action date for erenumab, a calcitonin gene-related peptide that the drugmakers plan to market under the name Aimovig.

    By July 21, 2017
  • Takeda shuffles sales force as restructuring continues

    The Japanese pharma has axed and relocated hundreds of sales positions as it continues to rejigger its portfolio. 

    By Suzanne Elvidge • July 19, 2017
  • PhRMA finally talks drug pricing in new campaign

    The trade group's newest campaign aims to tackle frequently asked drug cost questions, while also defending pharma's role in pricing decisions.

    By July 19, 2017
  • Sponsored by ZS Associates

    Patient centricity's challenges and opportunities

    Can pharma companies truly be patient-centric when they’re so far from the patient?

    July 18, 2017
  • J&J: Remicade holding up better than expected

    While second quarter sales slipped 14% for the anti-inflammatory drug, the big pharma noted that biosimilars played a muted role in that decline.

    By July 18, 2017
  • J&J's Tremfya approved, further crowding IL-inhibitor market

    Tremfya, approved to treat plaque psoriasis, will directly compete with Novartis' Cosentyx and Eli Lilly's Taltz.

    By July 14, 2017
  • Sunovion sheds asthma brands to focus on COPD

    The Massachusetts drugmaker recently acquired rights to three COPD treatments from Novartis and hopes to soon win approval for its own developed therapy. 

    By Suzanne Elvidge • July 14, 2017
  • Parkinson's drug Xadago launches in US

    US WorldMeds, which holds stateside commercialization rights to the drug, plans to have more than 60 sales reps support the launch.

    By July 12, 2017
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    Lisa LaMotta/BioPharma Dive
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    Allergan conflicted about teenage Botox market in light of growing demand

    Allergan CEO Brent Saunders spoke out against the use of medical aesthetic products for teenagers in a blog post this week, calling for stakeholders to start a conversation about the use of products in this age group.

    By Lisa LaMotta • July 12, 2017
  • Allergan has its eye on social media with #EyePic campaign

    Dublin, Ireland-based pharma Allergan strives to boost sales through its latest awareness push.

    By Suzanne Elvidge • July 12, 2017
  • Novartis hits pause on Fovista agreement

    The Swiss drugmaker is no longer obligated to develop and commercialize Ophthotech's drug, at least until data from the OPH1004 study becomes available.

    By July 10, 2017