🗓 Date: July 28, 2024 (Data presented) / Continued analysis up to 2025
📌 Source: Anavex Life Sciences – Phase IIb/III results presented at Alzheimer’s Association International Conference 2024, supplemented by Open-Label Extension (OLE) data
🧠 Trial Overview:
Drug: Blarcamesine (ANAVEX®2‑73), an oral sigma‑1 receptor agonist
Design: Phase IIb/III randomized, placebo-controlled trial in early Alzheimer’s patients across Europe, Australia, and North America
Duration: 48 weeks with open-label extension follow-up up to 192 weeks (~3.7 years)
📈 Major Findings:
Cognitive Decline Reduction: At 48 weeks, treatment groups experienced a 34.6–38.5% slower decline in ADAS‑Cog13 scores versus placebo
Delayed-Start Benefit: Early-start patients retained cognitive stability longer; Week 192 difference with delayed-start group was clinically significant (mean −3.83 points, P = 0.0165)
Brain Volume Preservation: Slowing of brain atrophy: total grey matter ~63.5%, whole brain ~37.6%, lateral ventricles ~25%
🩺 Safety Profile:
Well-tolerated overall, mostly mild-to-moderate adverse events during dose titration
No deaths or severe events attributed to Blarcamesine in long-term data
📢 Clinical Significance:
One of the first oral agents showing meaningful, long-term cognitive protection in early Alzheimer’s
Mechanism (sigma‑1 receptor modulation) differs from amyloid-targeting monoclonal antibodies, potentially safer with fewer hemorrhagic risks
Early initiation is key: “the earlier, the better” for slowing progression and preserving function
🚀 What’s Next:
Phase III registration trial is ongoing
Potential FDA/EMA submission expected in late 2025
If approved, could offer a low-cost, accessible Alzheimer’s therapy, significant for resource-limited settings
⚠️ Disclaimer: Blarcamesine is still under investigation and not yet approved by FDA or EMA. This information is for educational purposes only. Consult a healthcare professional for any treatment decisions.