Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Wednesday, August 28, 2024

Biogen announces discontinuation of Aduhelm

 

With our existing brain damage I can't see taking any drug that can possibly cause more brain damage. 

Biogen announces discontinuation of Aduhelm

Biogen announced a reprioritization of resources regarding its pipeline of therapeutics to address Alzheimer’s disease, deciding to discontinue development of Aduhelm and choosing to advance Leqembi.

According to a company release, Biogen will cease commercialization of Aduhelm in its 100 mg/mL IV formulation and will also end the ENVISION clinical study, a decision that Biogen said was unrelated to concerns about safety or efficacy. A significant portion of resources from the program termination will be placed back into Biogen’s AD franchise, the company additionally stated.

Older woman holding pills
Biogen announced it will shelve efforts to develop Aduhelm and instead concentrate on development and commercialization of Leqembi. Image: Adobe Stock

“We plan to further advance the launch of Leqembi together with Eisai and continue to bolster innovation with the development of the other assets in our pipeline,” Christopher A. Viehbacher, president and CEO of Biogen, stated in the release. “When searching for new medicines, one breakthrough can be the foundation that triggers future medicines to be developed.”

Biogen sought both partners and external financing for further development of Aduhelm beginning in January 2023, but during the extensive review and search process, could not identify either to satisfy their goals.

Aduhelm received accelerated approval from the FDA in June 2021, and the subsequent phase 4 ENVISION study was a requirement of that approval.

Biogen has recorded a one-time charge of approximately $60 million in close-out costs for the program. Biogen licensed Leqembi from Neurimmune and has terminated that license, with rights also reverting to Neurimmune.

Eisai currently heads the effort to develop Leqembi globally, whereas Eisai and Biogen jointly lead commercialization and promotion for the product and Eisai holds the final decision-making authority.

“We have gained significant insight from the development of Aduhelm and will carry this forward as we continue our pioneering work in Alzheimer’s disease,” Priya Singhal, MD, MPH, head of development at Biogen, said in the release. “We’d like to sincerely thank the trial investigators, health care providers, advocates, patients and families involved in the development of Aduhelm.”

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