This site uses cookies to improve your experience. To help us insure we adhere to various privacy regulations, please select your country/region of residence. If you do not select a country, we will assume you are from the United States. Select your Cookie Settings or view our Privacy Policy and Terms of Use.
Cookie Settings
Cookies and similar technologies are used on this website for proper function of the website, for tracking performance analytics and for marketing purposes. We and some of our third-party providers may use cookie data for various purposes. Please review the cookie settings below and choose your preference.
Used for the proper function of the website
Used for monitoring website traffic and interactions
Cookie Settings
Cookies and similar technologies are used on this website for proper function of the website, for tracking performance analytics and for marketing purposes. We and some of our third-party providers may use cookie data for various purposes. Please review the cookie settings below and choose your preference.
Strictly Necessary: Used for the proper function of the website
Performance/Analytics: Used for monitoring website traffic and interactions
A data-mining study conducted by researchers in the US has found that an already-approved diuretic drug could have potential as a treatment for some patients with Alzheimer’s disease.
Pharming has since started exploring new uses for the drug in acute kidney injury and COVID-19 pneumonia, whilst working on a gene therapy approach for HAE with Orchard Therapeutics. As it stands, the only other candidate for the disease listed in the clinicatrials.gov database is genericdrug rapamycin.
WASHINGTON — The Biden administration on Tuesday announced three new drug pricing policy experiments that would standardize how much Medicare patients pay for certain genericdrugs, pilot new ways for Medicaid to pay for pricey cell and gene therapies, and test ways to pay for drugs approved without proven clinical benefit to patients.
So where to start… Congresswoman Porter may want to look at the percentage of genericdrugs available virus branded (89%). Ex vivo (where cells are genetically modified outside the body) cell and gene therapies have generated considerable excitement on their potential to cure previously incurable diseases.
Indian pharma manufacturing continues to be the backbone of drug supplies worldwide, and GlobalData analysis suggests US overreliance on the country for genericdrug supply. US reliance on India for genericdrugs could have supply chain security and quality implications for critical medicines.
CSL closes deal for UniQure gene therapy in hopeful sign for M&A ( BioPharmaDive ).
Dyno raises $100 million to bring artificial intelligence to gene therapy ( STAT ).
Biogen’s Alzheimer’s drug may only be cost effective at $2,500 a year ( STAT ).
OcuWho? .
Alecensa is approved in Japan for the additional indication of recurrent or refractory ALK fusion gene-positive anaplastic large-cell lymphoma. Alecensa is not currently available in generic form. million the drug made during the same time in 2022. For the first three quarters of 2023, worldwide Alimta revenue was $172.6
Alecensa is approved in Japan for the additional indication of recurrent or refractory ALK fusion gene-positive anaplastic large-cell lymphoma. Alecensa is not currently available in generic form. million the drug made during the same time in 2022. For the first three quarters of 2023, worldwide Alimta revenue was $172.6
But all three drugs have new competitors. Meanwhile, BioMarin’s gene therapy Roctavian is approved by the FDA for the treatment of hemophilia A. Additionally, Bayer has formed a partnership with Mammoth Biosciences to broaden its product portfolio with innovative gene-editing technology. Both are anti-CD20 agents.
Gibbs — A recent blog post focused on the potentially negative implications of the proposed Patent Eligibility Restoration Act (PERA) for manufacturers of genericdrugs and biosimilar products. By 2010, about 2000 isolated human genes had been patented in the U.S. animal, viral, bacterial) DNA and RNA sequences.
Results are available in about 15 minutes, so the test is much faster than currently available tests which detect viral genes. If that supply chain dries up, Gibson predicts that the pharmacy shelves in the US would be empty within months and that hospitals across the US would cease to function.
We organize all of the trending information in your field so you don't have to. Join 21,000+ users and stay up to date on the latest articles your peers are reading.
You know about us, now we want to get to know you!
Let's personalize your content
Let's get even more personalized
We recognize your account from another site in our network, please click 'Send Email' below to continue with verifying your account and setting a password.
Let's personalize your content