Pharma: Page 50


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    Jacob Bell
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    José Baselga, prominent cancer researcher, dies at 61

    The head of AstraZeneca's oncology R&D changed the paradigm of breast cancer care by helping bring the targeted treatments Herceptin and Perjeta to patients. 

    By March 22, 2021
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    Courtesy of AstraZeneca
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    EU, UK throw support behind AstraZeneca's vaccine amid reports of rare blood clots

    The two drug regulators each believe the benefits of the shot outweigh the risks after investigating rare and unusual clotting events that have led more than 20 countries to halt vaccinations.

    By March 18, 2021
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    Brian Tucker / BioPharma Dive/BioPharma Dive
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    Trendline

    Top 5 stories from BioPharma Dive

    Looming patent expiries this decade and intensifying competition from China are forcing drugmakers to adapt, while new opportunities open up in oncology and in neuroscience.

    By BioPharma Dive staff
  • Xavier Becerra, nominee for HHS secretary, answers questions before the Senate Finance Committee.
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    Retrieved from C-SPAN on February 24, 2021
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    Becerra confirmed as HHS secretary

    The 50-49 vote in the Senate was almost entirely along party lines. The only Republican to cross the aisle was Sen. Susan Collins of Maine.

    By Shannon Muchmore • March 18, 2021
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    Kendall Davis/BioPharma Dive
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    Gilead, still aiming at NASH, broadens an alliance with Novo

    With positive safety data in hand, the partners will advance work pairing the diabetes medicine Ozempic with two experimental treatments to see if they can reverse the liver disease, which has proven a tough target for drugmakers.

    By March 18, 2021
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    Courtesy of Walmart
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    Biden administration hikes Medicare reimbursement for coronavirus vaccines

    The increased payout by Medicare is intended to speed up distribution of the three currently available shots.

    By Shannon Muchmore • March 16, 2021
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    Brian Tucker/BioPharma Dive
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    FTC joins overseas antitrust regulators in reexamination of pharma M&A

    Rebecca Kelly Slaughter, the commission's acting chair, indicated future reviews could look beyond measures of company size and market share.

    By March 16, 2021
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    Courtesy of Eli Lilly
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    Lilly lays out 2-year plan to gain approval for Alzheimer's drug

    Study results for donanemab showed signs of slowing disease progression, but the company believes the FDA won't review until another study confirms that apparent benefit.

    By March 15, 2021
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    Courtesy of AstraZeneca
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    AstraZeneca says 'no evidence' linking vaccine to clots after multiple countries pause rollout

    The drugmaker defended its shot following reports of blood clots among vaccine recipients, noting more than 17 million people in the U.K. and Europe have now received it.

    By March 15, 2021
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    Getty Images
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    Detailed Lilly data give mixed picture of Alzheimer's drug's benefit

    Highly anticipated results from a Phase 2 study of donanemab showed treatment slowed disease progression on one measure, but mixed data on other scales could temper optimism in its potential.

    By March 13, 2021
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    Alex Wong via Getty Images
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    The top drugs that could be impacted by an obscure provision in the pandemic relief law

    Elimination of the so-called penny rule in Medicaid could force drugmakers to pay larger rebates on a number of top medicines, including some HIV, diabetes and anti-inflammatory drugs.

    By March 12, 2021
  • A still of COVID-19 vaccine vials from Johnson & Johnson going through production
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    Permission granted by Johnson & Johnson
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    Vaccine factories churn out millions more doses, speeding US rollout of coronavirus shots

    The U.S. is now averaging more than 2 million doses given each day, a pace that will help President Joe Biden meet his target of 100 million shots in 100 days well ahead of schedule. 

    By March 11, 2021
  • A photo of Eli Lilly's quality control testing for bamlanivimab
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    Courtesy of Eli Lilly
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    Lilly builds case for COVID-19 drug cocktail with new data

    A low-dose combination of Lilly antibodies for COVID-19 reduced deaths and hospitalizations in a Phase 3 trial, a finding that could boost its use.

    By Kristin Jensen • March 10, 2021
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    Courtesy of Takeda
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    Taking a page from Celgene, Takeda builds and buys a cancer biotech

    An agreement to acquire Maverick Therapeutics for up to $525 million has roots in a plan hatched by Takeda to emulate elements of Celgene's dealmaking strategy.

    By March 9, 2021
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    Permission granted by Novartis
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    Novartis bid to bring rare disease drug to lung cancer hits a roadblock

    Promising signs from a cardiovascular trial had led the Swiss firm to test canakinumab, a drug for rare immune diseases, in lung cancer. But the first test of that theory has failed.

    By March 9, 2021
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    Permission granted by Roche
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    Spurred by FDA review, Roche pulls Tecentriq for bladder cancer use

    Four years after negative study results, the pharma withdrew the indication as the FDA's "industry-wide evaluation" of accelerated approvals progresses.

    By March 8, 2021
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    Courtesy of AstraZeneca
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    Crucial data on AstraZeneca's vaccine are coming. Here's what we may learn.

    Results from previous trials have raised questions about the vaccine and how well it works. Data from a large U.S. study could help clear up the confusion. 

    By March 8, 2021
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    Courtesy of Eli Lilly
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    Lilly says diabetes shot outperformed rival Novo drug in study

    The results are a boost for Lilly's drug, tirzepatide, which is being prepared for regulatory submissions later this year. But long-term heart data won't be available for some time.

    By March 4, 2021
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    Courtesy of Eli Lilly
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    Lilly drug regrows hair in autoimmune disease study, but safety questions linger

    The results could help baricitinib become the first treatment for alopecia areata, a leading cause of hair loss. Safety concerns have diminished the drug's prospects in arthritis, however.

    By March 3, 2021
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    Getty Images
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    Merck to help J&J make vaccine doses in White House-brokered deal

    The U.S. government will give Merck $269 million to help the drugmaker retool two of its facilities to make J&J's one-dose shot. 

    By Updated March 2, 2021
  • A sign reading Food and Drug Administration hangs over a building entrance.
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    Yujin Kim / MedTech Dive, original photo courtesy of U.S. Food and Drug Administration

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    Merck withdraws Keytruda in type of lung cancer amid 'industry-wide' review by FDA

    Since December, three drugmakers have withdrawn immunotherapies from indications previously granted fast-tracked approvals, suggestive of broader FDA concerns.

    By March 2, 2021
  • A still of COVID-19 vaccine vials from Johnson & Johnson going through production
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    Permission granted by Johnson & Johnson
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    J&J's 1-dose coronavirus vaccine becomes third available in US

    A CDC vaccine panel recommended use of the shot on Sunday following FDA authorization, and McKesson began shipping out doses to states Monday.

    By Updated March 1, 2021
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    Jacob Bell
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    AstraZeneca withdraws immunotherapy in bladder cancer after trial failure

    The British drugmaker's decision to pull Imfinzi from what was its first approved treatment setting hints at the limitations of immuno-oncology drugs.

    By Feb. 22, 2021
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    Sanofi Pasteur
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    Sanofi and GSK start trial of upgraded coronavirus vaccine after first version disappoints

    The companies think a new formulation will yield better results than their first attempt. But with several vaccines available, testing may be more challenging.

    By Feb. 22, 2021
  • A vial of BioNTech and Pfizer's coronavirus vaccine
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    Courtesy of BioNTech
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    Pfizer, BioNTech ask FDA approval to ease temperature requirements for coronavirus shot

    Testing showed the vaccine could be safely stored at normal freezer temperatures, rather than the roughly minus 70 degrees Celsius now specified. The change, if cleared by the agency, will help distribution.

    By Feb. 19, 2021
  • A building with logo of drugmaker Eli Lilly.
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    Courtesy of Eli Lilly
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    Lilly wagers almost $1B on Rigel's drugs for immune and nervous systems

    For $125 million up front, Lilly secures rights to a drug about to enter mid-stage testing for autoimmune and inflammatory diseases, as well as preclinical assets targeting the central nervous system.

    By Feb. 18, 2021