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
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
Pfizer and Valneva have been collaborating on VLA15’s development and commercialization since April 2020
The patent will lock in broad protection for the company’s lead therapy CardiolRx and its novel subcutaneous candidate CRD-38
Cardiovascular disease (CVD) is the leading cause of death in the US and worldwide with over 82 million Americans living with CVD
The FDA setback highlights ongoing tensions between patient needs, regulatory processes, and the use of real-world evidence in evaluating treatments for rare diseases
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