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Zydus to initiate phase II (a) trial of ZYIL1 in patients with CAPS in Australia

Our Bureau, Mumbai
Monday, December 13, 2021, 15:45 Hrs  [IST]

Zydus, a leading discovery-based global pharmaceutical company, has received permission to initiate the phase II (a) clinical study of its NLRP3 inhibitor "ZYIL1" in patients with Cryopyrin-Associated Periodic Syndrome (CAPS) in Australia.
Phase II (a) clinical trial in Australia will study the safety, tolerability, pharmacokinetics and pharmacodynamics in patients with Cryopyrin Associated Periodic Syndrome (CAPS).

 Cryopyrin-Associated Periodic Syndrome (CAPS) is caused by NLRP3 activating mutations that cause activation of the cryopyrin inflammasome and release of inflammatory cytokines including IL-1ß. Selective inhibition of NLRP3 could be beneficial, as NLRP3 inflammasomes are primarily involved in the inflammation process in these patients.
CAPS is a rare life-long auto-inflammatory condition, and is classified under orphan diseases. The chronic inflammation due to IL-1beta release in CAPS patients leads to urticaria-like rash, fever, arthralgia, and increased risk of amyloidosis.

 CAPS patients also experience multiple neurological complications like sensorineural hearing loss, migraine, headache, aseptic meningitis and myalgia. Bone deformities and neurological impairment have been reported in Neonatal Onset Multisystem Inflammatory Disease (NOMID), the most severe form of CAPS.

 Pankaj R. Patel, chairman, Cadila Healthcare Ltd. said, "The Cryopyrin Associated Periodic Syndromes (CAPS) patient community has very limited treatment options and there is a huge unmet medical need. We are committed to develop novel therapies, and ZYIL1 has potential to treat several autoimmune diseases."
ZYIL1 is a novel oral small molecule NLRP3 inhibitor. Studies have demonstrated that ZYIL1 has high binding affinity in human whole blood, and can selectively supress inflammation caused by the NLRP3 inflammasome. In non-clinical species including mice, rats and non-human primates, ZYIL1 has demonstrated brain penetration.
The efficacy of ZYIL1 has been established in a number of validated pre-clinical models of neuroinflammation, Parkinson's disease, inflammatory bowel disease (IBD), multiple sclerosis (MS), sepsis and acute lung injury models of acute respiratory distress syndrome (ARDS). The candidate, ZYIL1, has an acceptable ADME profile, with good safety margin.


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