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stroke

Human Amniotic Fluid Stem Cells Can Improve Cerebral Vascular Remodelling and Neurological Function after Focal Cerebral Ischaemia in Diabetic Rats

[Journal of Cellular and Molecular Medicine] Human amniotic fluid stem cells could enhance cerebral vascular remodelling and have the potential to improve neurological function after stroke in diabetic rats.

Hypoxic Postconditioning Promotes Neurogenesis by Modulating the Metabolism of Neural Stem Cells after Cerebral Ischemia

[Experimental Neurology] Researchers investigated whether hypoxic postconditioning (HPC) could promote neurogenesis after ischemic stroke, and to investigate the role of neuronal stem cell metabolism in HPC-induced neuroprotection.

PathMaker Neurosystems Announces Receipt of NIH Grant for Application of Its Non-invasive Neuromodulation Technology to Amyotrophic Lateral Sclerosis (ALS)

[nan] PathMaker Neurosystems, Inc. announced that it was awarded a Phase I STTR grant from NIH’s National Institute of Neurological Disorders and Stroke. The $371,000 award will enable the completion of key pre-clinical studies evaluating the effect of treatment with PathMaker’s breakthrough technology for motor neuron hyperexcitability suppression in transgenic ALS mice.

AIM/CD5L Attenuates DAMPs in the Injured Brain and Thereby Ameliorates Ischemic Stroke

[Cell Reports] Investigators reported that AIM protein reduced sterile inflammation by attenuating damage-associated molecular patterns and that AIM administration ameliorated the deleterious effects of ischemic stroke.

GNT Pharma Announces Approval of IND Application for the Phase III RODIN Trial of Nelonemdaz for Acute Ischemic Stroke Patients

[GNT Pharma Inc. (BusinessWire, Inc.)] GNT Pharma Inc. reported that the Korea Ministry of Food and Drug Safety has approved the Investigational New Drug Application for a phase III study of nelonemdaz for acute ischemic stroke patients.

US FDA Accepts for Priority Review Supplemental New Drug Application for Oxbryta® (Voxelotor) for the Treatment of Sickle Cell Disease in Children Ages 4...

[Global Blood Therapeutics, Inc.] Global Blood Therapeutics, Inc. announced that the US FDA has accepted for filing and review the company’s supplemental New Drug Application seeking accelerated approval for Oxbryta® for the treatment of sickle cell disease in children ages 4 to 11 years and its New Drug Application seeking approval for a new age-appropriate dispersible tablet dosage form of Oxbryta suitable for pediatric patients.

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