AL-S Pharma shows promising Phase 2 results for its therapy in ALS treatment
Adverse events were similar to placebo, and no AP-101-induced antibody responses were detected
Adverse events were similar to placebo, and no AP-101-induced antibody responses were detected
The partnership aims to develop novel, selective small molecules targeting TDP-43 pathology
This approval follows the CDE’s clearance in July of this year for Phase 2/3 clinical studies of CB03-154 in amyotrophic lateral sclerosis
As part of its partnership with Dr. Reddy’s Laboratories (DRL), FDA acceptance also triggers a $4.2 million milestone payment to Coya
The company reported revenue from operations at Rs. 6,573.7 crore, up 6 per cent YoY
Usnoflast has previously also received ‘Orphan Drug Designation (ODD)’ from the USFDA
The company is committed to unlocking new frontiers in neuroscience and developing Usnoflast for patients with ALS
This study will enrol 210 ALS patients and study doses of 50 mg and 75 mg Usnoflast versus placebo
ALS patients experience neuroinflammation and rapid neurodegeneration
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