AC Immune Announces Positive Preliminary Phase 1 Data for NLRP3 Inhibitor ACI-19764
AC Immune Announces Positive Preliminary Phase 1 Data for NLRP3 Inhibitor ACI-19764
- ACI-19764 is an orally available inhibitor of the NLRP3 inflammasome
- Preliminary data showed ACI-19764 was safe and well tolerated across single and multiple ascending dose cohorts with confirmed CSF penetration
- Based on PK data the therapeutic dose is expected to be ≤10mg once daily
- To rapidly evaluate the anti-inflammatory activity of ACI-19764 (effect on hsCRP), dosing of a cardiovascular risk cohort is now underway with initial results expected by year end
- Full results from the Phase 1/1b trial are expected in H1 2027
Lausanne,
The Phase 1 study is investigating the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics of ACI-19764 in healthy volunteers in
The trial has now commenced dosing of first patients with cardiovascular disease risk, as determined by elevated serum levels of high-sensitivity C-reactive protein (hsCRP) and the presence of either type 2 diabetes and/or obesity. Recruitment of this Phase 1b cohort is ongoing and initial results are expected before year end.
ACI-19764 targets the NLRP3 inflammasome to inhibit the production of pro-inflammatory factors and reduce chronic inflammation thought to be associated with disease progression in multiple inflammatory disorders, metabolic diseases, and neurological diseases. Supported by a strong preclinical data package (including 3-month toxicology data), ACI-19764 continues to advance through its Phase 1/1b clinical study, with additional data expected in H1 2027.
About ACI-19764
ACI-19764 is an orally available, brain penetrant, small molecule drug candidate which specifically inhibits the NLRP3 inflammasome. It has shown high potency in vitro as demonstrated by the downstream inhibition of IL-1β production by human macrophages and human whole blood with an IC50 in the range of 2-20.5nM. ACI-19764 statistically significantly inhibited neuroinflammation in vivo through reduced activation of Iba1+ microglial cells and GFAP+ astrocytes in preclinical models (including experimental autoimmune encephalitis (EAE) and chronic LPS-mediated central nervous system (CNS) inflammation), demonstrating its strongly competitive profile and high potential for broad application in both peripheral and neurologic therapeutic areas.
About AC Immune SA
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Source: AC Immune SA