Chromos says preclinical data supports MS drug
In addition, the data validates VLA-2 as a potential target for early therapeutic intervention in the treatment of multiple sclerosis (MS). “Currently, there are no FDA approved therapies
The US Food and Drug Administration (FDA) has granted accelerated approval to Bristol Myers Squibb’s (BMS) Zenbexus (iberdomide), along with daratumumab and hyaluronidase-fihj and dexamethasone (ZDd), to treat adult multiple myeloma (MM) patients.