ABBV-0805 is under clinical development by BioArctic and currently in the Phase I in clinical pathway. The characteristics of the clinical trial as well as other attributes related to the drug, regulations, and company play a fundamental role in ensuring the likelihood of transition that the drug moves from its current development stage to next.
According to GlobalData, the latest event to affect ABBV-0805’s likelihood of approval (LoA) and phase transition for Parkinson’s Disease took place on 21 Apr 2022, which decreased the likelihood that the drug progresses to the next phase in its clinical pathway and decreased the likelihood of final approval for this indication.
GlobalData uses proprietary data and analytics to provide a complete picture of this assessment in their ABBV-0805 Likelihood of Approval (LoA) and Phase Transition Success Rate (PTSR) Report.
ABBV-0805 overview
ABBV-0805 (BAN-0805) is under development for the treatment of Parkinson's disease. The drug candidate is a monoclonal antibody which acts by targeting aggregated/misfolded protein called alpha-synuclein. It is developed based on antibody technology. It was also under development for the treatment of dementia with Lewy bodies. It is administered through intravenous route.
BioArctic overview
BioArctic, formerly BioArctic Neuroscience, is a biopharma company that develops new immunotherapeutic treatments for patients with central nervous system disorders. The company develops drugs for neurological disorders such as Parkinson’s disease, Alzheimer’s disease, and spinal cord injury. It develops alzeimer antibodies. BioArctic’s reagents include AB antibody AbetaN, Alzheimer biomarker and parkinson biomarker. The company’s antibodies have the capability to reduce soluble, toxic aggregated proteins in the brain. It develops new treatments for Parkinson’s disease and Dementia with Lewy bodies. The company collaborates with research groups at universities and hospitals. BioArctic is headquartered in Stockholm, Sweden.
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