Blarcamesine

Anavex Life Sciences announced EMA accepted blarcamesine's MAA for Alzheimer's treatment, supported by Phase IIb/III trial data showing 48-week ADAS-Cog13 score >2 points. Blarcamesine, an oral once-daily drug, activates SIGMAR1, inducing autophagy for cellular homeostasis, with a favorable safety profile and no routine MRI monitoring.

Anavex Life Sciences Corp. reported Q4 and fiscal year 2024 results, highlighting progress in Alzheimer's treatment with blarcamesine (ANAVEX®2-73), including EMA MAA submission and clinical trial data. Financials show $132.2M cash, with a 4-year runway. Upcoming events include a webcast and J.P. Morgan 2025 Healthcare Conference presentation.

Anavex Life Sciences' MAA for blarcamesine, a potential Alzheimer's treatment, accepted by EMA for review, marking progress towards wider patient access in Europe.

10 biotech companies to watch in 2025: Anavex Life Sciences (blarcamesine for neurodegenerative diseases), Candid Therapeutics (T cell engager antibodies for autoimmune diseases), Enterprise Therapeutics (ETD001 for cystic fibrosis), Jazz Pharmaceuticals (Ziihera for biliary tract cancer), Life Biosciences (ER-100 for optic neuropathies), Ovid Therapeutics (OV888 for cerebral cavernous malformation), Skye Bioscience (nimacimab for obesity), TG Therapeutics (Briumvi for multiple sclerosis), Wave Life Sciences (WVE-006 for alpha-1 antitrypsin deficiency), and Quotient Therapeutics (somatic genomics platform for drug discovery).

DelveInsight's report on Alzheimer's Disease pipeline highlights 110+ companies developing 120+ therapies, including key players like Neurodon, Sangamo Therapeutics, and Eisai Co Ltd. Notable therapies in clinical trials are NRDN-201, ST-501, and Simufilam. Recent developments include FDA approval of Leqembi and ongoing Phase 1 trials for ML-007/PAC by MapLight Therapeutics. The report covers pre-clinical to marketed phases, detailing drug MOA, ROA, and market dynamics.

ShiraTronics launched RELIEV-CM2 study for chronic migraine; QurAlis' QRL-201 enters dose range-finding phase for ALS; Anavex submits marketing authorization application for blarcamesine in Alzheimer's disease.

Anavex Life Sciences submitted a marketing authorization application for blarcamesine, a potential Alzheimer's treatment, based on phase 2/3 AD-004 trial data showing significant cognitive decline slowing. The drug reduced brain atrophy and showed safety with manageable side effects.

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Anavex Life Sciences Corp. ($AVXL) shares surged 11% in pre-market trading after filing for EMA approval of its oral Alzheimer's drug, blarcamesine. The drug showed significant improvement in ADAS-Cog13 scores over 48 weeks, potentially slowing cognitive decline. Anavex claims blarcamesine is more effective and easier to use than existing therapies. Retail sentiment on Stocktwits was 'extremely bullish' following the EMA submission.

Anavex Life Sciences Corp. submitted blarcamesine (ANAVEX®2-73) MAA to EMA for Alzheimer's Disease treatment, showing clinically meaningful improvement over 48 weeks with a primary endpoint ADAS-Cog13 score >2 points, suggesting superior efficacy and neurodegeneration slowing in early AD patients. Blarcamesine, an oral small molecule, does not require routine MRI monitoring and has an appealing safety profile. Europe's Alzheimer's disease population is expected to double by 2030, with a 2019 care cost of $439 billion.