Citing unanticipated delay in the collection of study data, Can-Fite BioPharma Ltd CANF said that the topline data from its Phase 3 Comfort study of Piclidenoson in severe plaque psoriasis would be released in Q2 2022.
- Earlier, the data were anticipated in Q1 of 2022.
- The study enrolled more than 400 patients across 30 sites in Europe, Israel, and Canada.
- Piclidenoson is an A3 adenosine receptor agonist (A3AR) small molecule that inhibits interleukin-17 and interleukin-23, both pivotal for the formation of skin lesions.
- Piclidenoson has also recently been shown to induce the death of pathological skin cells.
- The Comfort study's primary endpoint is the proportion of patients who achieve a PASI score response of ≥75% (PASI 75) vs. placebo at week 16. Secondary endpoints include non-inferiority to Amgen Inc's AMGN Otezla (apremilast).
- Also See: Can-Fite Shares Rally As Namodenoson Clears All Cancer Lesions In Liver Cancer Patient.
- Price Action: CANF shares are down 7.21% at $1.03 during the premarket session on the last check Tuesday.
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