Developing angina drug shows promise in trial with no patient headaches

The drug is aimed at treating chronic stable angina pectoris and conducted in Portugal, the exploratory phase 1a pharmacokinetics study​, involving 16 healthy adult volunteers, concluded just before the end of last year (2023).

The study focused on evaluating the pharmacokinetics of AUX-001, an oral, extended-release, once-daily version of nicorandil, a medication used to treat angina. Additionally, it aimed to assess the safety and tolerability of the investigational anti-anginal drug.

The topline results of the study demonstrated that AUX-001 effectively prolonged the half-life of nicorandil from the standard 49±8 minutes, as observed with the current immediate-release form administered twice daily, to over nine hours.

Dawid Chabowski, science and operational manager at Auxilius Pharma, said: “A result like this bodes well for AUX-001’s potential to extend daylong coverage of its anti-ischemic effect with just one capsule a day.”

The study revealed that AUX-001 was well-tolerated by participants, with headaches being the most common adverse event.

Auxilius chief medical officer, Uwe Tigör, emphasized the significance of managing headaches, he said: “Ours is probably one of very few angina studies using oral nicorandil with no headache related patient dropouts, thanks to our preemptive management and proactive patient communication.”

The successful outcomes of this trial mark a significant milestone for Auxilius Pharma’s R&D efforts. CEO Jed Litwiniuk is confident in the trial’s results. He said: “We are reassured by the outcomes of the trial.”

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