Bayer advances fight against rare kidney disease with new experimental drug
Alport Syndrome is caused by genetic mutations affecting type IV collagen in the kidneys, ears, and eyes
Alport Syndrome is caused by genetic mutations affecting type IV collagen in the kidneys, ears, and eyes
AEF0217 is a first-in-class CB1 receptor signaling-specific inhibitor
Here's a new ray of hope for new hope for patients suffering from Meniere’s disease (MD) and sensorineural hearing loss
Seeing well-controlled Phase 3 data that shows a marked slowing of lesion growth in Stargardt disease is deeply encouraging
Soficitinib is a potent and selective TYK2 inhibitor under development for multiple T-cell mediated autoimmune disorders
Centanafadine is a first-in-class norepinephrine, dopamine, and serotonin reuptake inhibitor
Itvisma is a one-time, fixed-dose therapy designed to tackle the genetic root cause of SMA
The formulation is backed by over 80 clinical trials and 200 scientific publications
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