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.

Friday, January 19, 2024

FDA clears investigational new drug application for novel stroke therapy

So I can't find any earlier research on animals that says what this is trying to fix. So go ask your competent? doctor what this will be doing for recovery.

FDA clears investigational new drug application for novel stroke therapy

Key Takeaways:

  • AB126 is an unmodified neural-derived exosome developed to treat acute ischemic stroke.
  • A planned phase 1b/2a clinical trial is expected to start in the first half of 2024.

The FDA has cleared an investigational new drug application for an unmodified neural-derived exosome to treat those with acute ischemic stroke, according to its manufacturer.

In a press release, Aruna Bio Inc. said the FDA’s decision will allow its lead program, AB126, which can cross the blood-brain barrier, to be examined in a pending phase 1b/2a study that is expected to begin during the first half of this year.

Generic FDA News infographic
The FDA cleared an IND from Aruna Bio for a novel IV therapy for those with acute ischemic stroke. Image: Adobe Stock

The dose-ascending clinical trial will evaluate safety, tolerability and preliminary efficacy of AB126 in those with acute ischemic stroke who have previously undergone a thrombectomy. All participants in the trial — including those with a poor post-thrombectomy prognosis — will receive three IV treatments of AB126 at low, medium and high doses, per the release.

“We are thrilled with this validation from the FDA,” Steven Stice, PhD, co-founder and chief scientific officer of Aruna, said in the release. “Further, maintaining cells under controlled conditions is a key aspect of exosome manufacturing, and we look forward to leveraging our in-house manufacturing expertise to support clinical advancement.”

Aruna added that it plans to expand AB126’s applications to include amyotrophic lateral sclerosis as well as to explore broader potential of its neural exosome platform to address ongoing challenges in treating central nervous system conditions.

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