Lilly Reports Negative Results of Solanezumab in P-III EXPEDITION Studies in Patients with Alzheimer Disease
Shots:
- The P-III EXPEDITION Study involves assessing of Solanezumab (400 mg- IV- q4w) vs PBO in 1-012 (EXPEDITION1) & 1-040 (EXPEDITION2) patients with mild or mild to moderate Alzheimer disease
- The study resulted in unmet endpoint and demonstrated 42% reduction in decline- 20% reduction in cognitive decline- 19 percent reduction in functional decline in patients
- Solanezumab is a monoclonal IgG1 Ab- evaluated as a neuroprotector in patients with Alzheimer disease
Ref: Eli Lilly | Image: The Street
Click here to read the full press release
This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com