German pharmaceutical and life sciences company Bayer AG (ETR:BAYN) (OTC:BAYRY) announced on Thursday that it has initiated a Phase IIa clinical trial of BAY 3401016, an investigational monoclonal antibody designed to block Semaphorin 3A (Sema3A), a protein implicated in kidney damage in Alport Syndrome (AS).
The ASSESS study is a randomised, double-blind, placebo-controlled trial with an extension phase, evaluating the safety and efficacy of BAY 3401016 in adults with rapidly progressing AS.
Alport Syndrome is a rare genetic disorder caused by mutations affecting type IV collagen, leading to proteinuria, progressive kidney failure, and early onset of end-stage renal disease. Currently, there is no specific treatment approved for AS.
Diagnosis occurs via urine tests, kidney biopsy, or genetic testing, and disease progression varies, often affecting men earlier while women may experience milder or later onset symptoms.
Bayer's BAY 3401016 programme builds on a strategic research collaboration with Evotec and represents a key addition to the company's development portfolio for rare kidney diseases. The programme has received both Fast Track Designation and Orphan Drug Designation from the US Food and Drug Administration (FDA).
The new Phase IIa trial aims to determine the potential of BAY 3401016 to slow kidney function decline in adult AS patients, addressing a high unmet medical need.
Karyopharm seeks accelerated FDA approval for selinexor–ruxolitinib in myelofibrosis
Ascletis Pharma Inc doses first participant in global Phase III clinical programme of ASC30
Zambon receives European Commission approval for Hopledo in Parkinson's disease
Pfizer and BioNTech granted FDA approval for XFG-adapted COVID-19 vaccine
Annovis Bio schedules corporate update webinar for next week
Cellenkos' CK0803 granted US FDA Fast Track designation for ALS
Labcorp to offer FDA-cleared pTau-217 blood test for Alzheimer's assessment
Tempus announces receipt of FDA clearance for AI pulmonary hypertension detection product
European Commission grants orphan designation for Vanda's imsidolimab
United Therapeutics wins FDA acceptance for ralinepag PAH filing
Acadia wins EU approval for DAYBU as first treatment for Rett syndrome