Action Pharma’s phase IIb clinical trial with AP214 to prevent kidney injury demonstrates positive top-line results
- Statistically significant improvement in clinical outcomes based on a 90 day composite endpoint (death, dialyses, and kidney function) compared to placebo – a possible endpoint for registration trials based on the Company’s previous discussions with the FDA
- Statistically significant improvement in GFR (glomerular filtration rate) at day 90 compared to baseline
- Lower incidence of acute kidney injury (AKI) within 48 hours (AKIN score) or 7 days (RIFLE score)
- Lower serum creatinine levels at day 7
Furthermore, AP214 was safe and well-tolerated comparable to placebo. The clinical results are expected to be presented as late breaking clinical abstract at the annual meeting of the ASN (American Society of Nephrology) to be held on November 8-13 in Philadelphia, PA, USA.
"These positive phase IIb clinical data are potentially very good news for patients", says Ingelise Saunders, CEO of Action Pharma. She continues, “based on the positive results we will now accelerate our discussions with major pharmaceutical companies focused on this group of high risk patients.”
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