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, October 29, 2025

‘Designer Drug’ Shows Early Neuroprotective Signal in Acute Ischemic Stroke

 Your competent? doctor has created protocols on the use of IGF-1 years ago, right?

  • IGF-1 (19 posts to March 2014)
  • Do you prefer your doctor, hospital and board of director's incompetence NOT KNOWING? OR NOT DOING?

    ‘Designer Drug’ Shows Early Neuroprotective Signal in Acute Ischemic Stroke

    BARCELONA, Spain — An experimental drug that takes a novel approach to protecting injured brain cells has shown promising results in an early Phase 2 trial of patients with acute ischemic stroke (AIS).

    Known as Scp776, the drug is based on insulin-like growth factor 1 (IGF-1), which plays a key role in brain health by protecting neurons from excitotoxicity, hypoglycemic damage, oxidative stress, inflammation, and apoptosis.

    In the Phase 2a ARPEGGIO study, the drug showed preliminary signs of neurologic improvement compared with placebo in patients with large-vessel occlusion (LVO) stroke treated within the late time window (up to 24 hours after symptom onset).

    Those treated with Scp776 showed a trend toward better National Institutes of Health Stroke Scale (NIHSS) scores, which measure stroke severity, at 7 days, and improved modified Rankin Scale (mRS) scores, which assess functional outcomes, at 90 days.

    The drug also appeared to be safe and well tolerated with no serious adverse events compared with placebo.“This is a unique and innovative drug, and these early results are very exciting” lead investigator of the ARPEGGIO trial, study investigator, Eva Mistry, MD, associate professor of neurology at the University of Cincinnati, Cincinnati, told Medscape Medical News.

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