Pharma: Page 50
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Courtesy of Eli Lilly
Lilly ups revenue forecast amid windfall from COVID-19 drugs
While the boost from its COVID-19 treatments might be temporary, Lilly believes next year's revenue will hold up thanks to newer products. Also on the horizon are potential approvals for key Alzheimer's and diabetes medicines.
By Jacob Bell • Dec. 15, 2021 -
Permission granted by Bristol-Myers Squibb
Bristol Myers returns to Immatics for a dual-targeting cancer drug
The pharma has expanded an alliance with a German biotech by paying $150 million for a drug candidate that executives hope can have "cell therapy-like efficacy" for solid tumors.
By Ben Fidler • Dec. 14, 2021 -
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Brian Tucker / BioPharma Dive/BioPharma Dive
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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 -
Permission granted by Roche
Latest Roche results show promise for new type of cancer immunotherapy
Updated Phase 2 data suggested an experimental drug targeting the protein TIGIT could bolster the benefit of Roche's Tecentriq in certain people with advanced lung cancer.
By Ben Fidler • Dec. 10, 2021 -
Courtesy of AstraZeneca
AstraZeneca antibody cleared by FDA for preventive use against COVID-19
Evusheld, a combination of two antibodies, is meant to be long-acting, proving protective against disease through six months in clinical testing.
By Ned Pagliarulo • Dec. 8, 2021 -
National Institute of Allergy and Infectious Diseases. (2020). "Novel Coronavirus SARS-CoV-2" [Micrograph]. Retrieved from Flickr.
Vaccine from Medicago, GSK protective against COVID-19 in large study
The vaccine, which Medicago plans to soon submit to Canadian regulators, would be the first of its type, though supply appears likely to be limited.
By Jonathan Gardner • Dec. 7, 2021 -
Courtesy of Eli Lilly
Lilly drug becomes first COVID antibody cleared for use in young children
The emergency clearance from the FDA allows for treatment of mild and moderate disease as well as prevention in those exposed and at high risk.
By Jonathan Gardner • Dec. 6, 2021 -
Permission granted by Novartis
Novartis pays $150M for access to UCB's Parkinson's drug
UCB's experimental pill is one of the most advanced projects that's aimed at blocking accumulation of an abnormal protein in patients' brains.
By Jonathan Gardner • Dec. 2, 2021 -
Courtesy of Merck & Co.
FDA panel, after debate, narrowly backs Merck COVID pill
While agency advisers raised concerns over molnupiravir's modest benefits and potential risks, a majority felt the antiviral drug is a needed option for COVID-19 patients at high risk of severe disease.
By Jonathan Gardner • Updated Nov. 30, 2021 -
Warren Little via Getty Images
GSK hires away top Pfizer vaccine scientist
Philip Dormitzer, who helped Pfizer develop shots for COVID-19, RSV and influenza, will become the British pharma's head of vaccine R&D next month.
By Ned Pagliarulo • Nov. 30, 2021 -
National Institute of Allergy and Infectious Diseases. (2020). "Novel Coronavirus SARS-CoV-2" [Micrograph]. Retrieved from Flickr.
Vaccine makers move quickly to confront omicron threat
Several companies, including Pfizer and Moderna, are already at work adapting their coronavirus shots to the newly identified variant, which experts worry could more readily evade vaccine protection.
By Ned Pagliarulo • Nov. 29, 2021 -
Courtesy of Merck & Co.
New Merck study results raise questions about its COVID pill
Final trial data for molnupiravir were less convincing than what Merck previously reported and could alter how the FDA views the drug, which will be evaluated at a meeting Tuesday.
By Ben Fidler • Nov. 26, 2021 -
Getty Images
Takeda wins US approval for new CMV treatment
The antiviral drug, which has been a top research focus of Takeda for years, is the first to be cleared by the FDA for post-transplant CMV infections that are resistant to other treatments.
By Kristin Jensen • Nov. 24, 2021 -
Courtesy of AstraZeneca
AstraZeneca, after years of delays, opens UK hub meant to recharge drug research
Formally unveiled five years after originally planned, the $1 billion headquarters will become the British drugmaker's second-largest R&D center by headcount.
By Jonathan Gardner • Nov. 23, 2021 -
Antonio Masiello via Getty Images
Pfizer, BioNTech to seek full approval as COVID-19 vaccine efficacy holds up in young teens
Four months after vaccination, no 12- to 15-year-olds in the companies' clinical trial developed COVID-19, compared to 30 who received a placebo.
By Ben Fidler • Nov. 22, 2021 -
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Sponsored by AltasciencesNanomilling: an optimal solution for poorly soluble, challenging APIs
A versatile technique to ensure your drug is ready on time for your first-in-human clinical trial.
Nov. 22, 2021 -
A worrisome safety signal slows Merck's HIV ambitions
After a study raised safety concerns, Merck has paused development of one of its experimental drugs and will keep a close eye on another that's critical to its plans in HIV.
By Jacob Bell • Nov. 19, 2021 -
Sarah Silbiger via Getty Images
FDA, aiming to curb another COVID-19 surge, clears Pfizer, Moderna boosters for all adults
A monthslong process of authorizing booster shots for vulnerable Americans culminated in the FDA's Nov. 19 decision to open eligibility for all adults, now all the more critical with omicron's spread.
By Ben Fidler • Updated Nov. 20, 2021 -
Permission granted by Gilead Sciences
Gilead pays up to retain rights to Arcus cancer drugs
The biotech will pay $725 million to opt into rights on four experimental medicines developed by Arcus, including ones that could challenge Merck's Keytruda in lung cancer.
By Jonathan Gardner • Nov. 18, 2021 -
FDA approves Merck's Keytruda as first immunotherapy for early kidney cancer
Immune-boosting drugs like Keytruda are increasingly being tested, and proven effective, alongside surgery before tumors spread widely.
By Ben Fidler , Ned Pagliarulo • Nov. 18, 2021 -
Permission granted by Roche
Roche cuts ties with Atea after COVID-19 pill's trial failure
The Boston biotech, shares of which soared last year on hopes for the antiviral drug, said it has plenty of money to advance development on its own.
By Kristin Jensen • Nov. 17, 2021 -
Jeenah Moon via Getty Images
Pfizer asks FDA to authorize COVID-19 pill
Study results released this month showed the pill, when given soon after symptoms start, sharply reduced the risk of COVID-19 hospitalization or death.
By Ned Pagliarulo • Nov. 16, 2021 -
Getty Images
As Congress weighs drug price restraints, ICER calls out 'unsupported' increases
In a new report, ICER highlighted AbbVie's price hikes on Humira, which the group said resulted in more than $1 billion in U.S. spending last year without any new evidence of health benefits.
By Jonathan Gardner • Nov. 16, 2021 -
Spencer Platt via Getty Images
Pfizer will allow generic drugmakers to produce promising COVID-19 pill
A licensing deal with a U.N.-backed patent group could expand supply of Pfizer's experimental drug Paxlovid in lower- and middle-income countries.
By Ned Pagliarulo • Nov. 16, 2021 -
Permission granted by IQVIA
Sponsored by IQVIAEstablishing an integrated evidence plan for medical affairs and beyond
Over the life of a biopharmaceutical product, there are many situations when data from randomized controlled trials (RCTs) may not be sufficient to address stakeholder questions of value, safety and effectiveness.
Nov. 15, 2021 -
Mario Tama via Getty Images
J&J, world's largest drugmaker, plans to split in two
The industry giant and mainstay of corporate America will separate its consumer health business from its drug and medical device units, which will retain the J&J brand.
By Ben Fidler , Ned Pagliarulo • Updated Nov. 12, 2021
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