Zydus Receives Approval For ALS Phase II Trial Of ZYIL1
Zydus, a pharmaceutical company, received permission from The Central Drugs Standard Control Organisation (CDSCO), to initiate the Phase II clinical study of NLRP3 inhibitor “ZYIL1” in patients with Amyotrophic Lateral Sclerosis (ALS), the company said in an exchange filing on Wednesday. The USFDA has granted Zydus an ‘Orphan Drug Designation’ for ZYIL1 to treat patients with Cryopyrin Associated Periodic Syndrome (CAPS), a rare auto-inflammatory disease, the company said.
ALS patients experience neuroinflammation and rapid neurodegeneration leading to a steady loss of the ability to move, speak, eat and eventually breathe. ALS results in the loss of motor neurons in the brain and spinal cord which controls voluntary muscle movement. ALS affects approximately 31,000 people in the U.S.A and on average 5,000 new patients are diagnosed every year with this disease in the USA as per statistics from the Centers for Disease Control and Prevention (CDC).
More than 30,000 people are estimated to be living with ALS in Europe (European Union and United Kingdom), while India has an estimated 75,000 people living with ALS. People living with ALS have a median survival of approximately two years from diagnosis, the statement from the company informed.
Pankaj R. Patel, Chairman, of Zydus Lifesciences said, “Zydus has always aimed at improving the quality of life of patients through its life-changing discoveries. This study is a positive step in this direction to address the very high unmet medical needs of patients suffering from ALS. By targeting neuroinflammation and neurodegeneration with ZYIL1, we hope to open up new possibilities in treating ALS.”
The company further stated that the Phase II clinical trial will study safety, tolerability, pharmacokinetics and pharmacodynamics in patients with ALS. The change from baseline in the Revised Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS-R) score will be measured at week 4, week 8 and week 12, as the trial’s primary endpoint is the placebo-controlled, randomised, double-blind Phase 2 clinical trial. The trial will also evaluate Key Secondary Endpoints including Slow Vital Capacity (SVC), a predictor of functional loss in ALS and neurofilament levels at week 4 and week 12.
ZYIL1 is a novel oral small molecule NLRP3 inhibitor, the company informed. Studies have demonstrated that ZYIL1 is highly potent in human whole blood assay and can suppress inflammation caused by the NLRP3 inflammasome. ZYIL1 was found distributed in the brain and CSF of various nonclinical species including mice, rats and non-human primates.
In Phase I studies, ZYIL1 was found to be safe and well-tolerated. Zydus has established the Phase 2 proof-of-concept in CAPS patients and has now published the data in Clinical Pharmacology in Drug Development, the company said in its statement.
