First-in-Human Phase I Clinical Trial of the Adenosine A1R/A3R Agonist AST-004 in Healthy Subjects

AST-004 was safe and well-tolerated at plasma concentrations 3 to 8× higher than those associated with significant efficacy in astrocyte's preclinical primate stroke efficacy studies, with CSF concentrations highest at the 60-minute collection timepoint, the last timepoint tested. This study supports additional clinical investigations, including evaluation of an extended infusion to support the phase 2 program in stroke and traumatic brain injury.

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Publication Details

Journal
Stroke
Published
2024-10-25
DOI
https://doi.org/10.1161/strokeaha.124.047207
Citations
4
Primary Topic
Adenosine and Purinergic Signaling
Type
article
Field-Weighted Citation Impact
1.61
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article

First-in-Human Phase I Clinical Trial of the Adenosine A1R/A3R Agonist AST-004 in Healthy Subjects

Theodore E. Liston, Robert Lancey, Juan Hernandez, Mark Matson et al.
4 citations
Stroke
Adenosine and Purinergic Signaling
1.61
article

First-in-Human Phase I Clinical Trial of the Adenosine A1R/A3R Agonist AST-004 in Healthy Subjects

Theodore E. Liston, Robert Lancey, Juan Hernandez, Mark Matson, Laura Manna, Dawn E. Hunt, William S. Korinek, Russell B. Poe, G Lakner
article en
4 citations

Abstract

AST-004 was safe and well-tolerated at plasma concentrations 3 to 8× higher than those associated with significant efficacy in astrocyte's preclinical primate stroke efficacy studies, with CSF concentrations highest at the 60-minute collection timepoint, the last timepoint tested. This study supports additional clinical investigations, including evaluation of an extended infusion to support the phase 2 program in stroke and traumatic brain injury.

StrokeVol. 55(12)
MACOM (United States) (US), Kista Photonics Research Center (SE)
Good health and well-being
Openalex Percentile: Top 17%
Adenosine and Purinergic Signaling
1.61
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