This week’s Neuroscience update highlights regulatory progress, clinical data readouts, early-stage research advances, and ongoing strategic pipeline and commercial developments.
In Today’s Newsletter
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In Today’s Newsletter
🧠 SciSparc, NeuroThera and Clearmind file depression therapy patent [1] [Hong Kong, China • 16 Mar 2026]
https://www.manilatimes.net/2026/03/16/tmt-newswire/globenewswire/scisparc-neurothera-labs-clearmind-medicine-collaboration-leads-to-patent-application-for-depression-therapy/2300775
Context: Clearmind Medicine and NeuroThera Labs are collaborating on a combination of MEAI and palmitoylethanolamide (PEA) for major depressive disorder.
Key point: Clearmind filed a patent application in Hong Kong, China, covering the MEAI–PEA combination therapy for depression.
Implication: Signals pipeline investment and modality expansion.
🧪 Oragenics explores CNS asset expansion around ONP-002 [2] [US • 11 Mar 2026]
https://ir.oragenics.com/press-releases/detail/228/oragenics-explores-expansion-of-cns-platform-pursuing
Context: Oragenics said ONP-002 Phase IIa is in active site initiation in Australia, with additional sites in governance review before enrollment.
Key point: Oragenics is exploring potential CNS asset acquisitions focused on brain health, brain recovery, and neuroprotection, but no definitive agreement has been reached.
Implication: Signals pipeline investment and modality expansion.
💼 NurExone adds adviser and closes financing [3] [Canada • 11 Mar 2026]
https://www.manilatimes.net/2026/03/11/tmt-newswire/globenewswire/nurexone-announces-corporate-updates/2297881
Context: NurExone develops exosome-based regenerative therapies for central nervous system injuries and said the placement remains subject to regulatory approval.
Key point: NurExone announced a consulting agreement with former Bayer scientist Lars Bärfacker, finalist status in the 2026 BOLD Awards Healthcare category, and a C$880,750.96 private placement.
Implication: Signals pipeline investment and modality expansion.
🏥 Plus Therapeutics maps 2026 milestones for REYOBIQ and CNSide [4] [US • 12 Mar 2026]
https://www.theglobeandmail.com/investing/markets/stocks/PSTV-Q/pressreleases/36541438/plus-therapeutics-reports-2025-results-business-progress-and-2026-anticipated-milestones-for-reyobiq-clinical-program-and-cnside-commercial-rollout/
Context: Plus reported year-end 2025 cash and investments of $13.1 million and highlighted reimbursement, coverage, and lab licensing progress for CNSide.
Key point: Plus said it expects 2026 readouts and operational milestones across REYOBIQ trials, manufacturing scale-up, and CNSide commercial expansion.
Implication: May influence prescriber choice and payer reviews pending full data.
🧬 Amlogenyx reports preclinical Alzheimer’s data for AM805 [5] [US • 16 Mar 2026]
https://www.manilatimes.net/2026/03/16/tmt-newswire/globenewswire/amlogenyx-announces-positive-preclinical-data-on-am805-a-potent-amyloid-degrading-protease-for-the-treatment-of-alzheimers-disease/2300792
Context: AM805 is an investigational AAV9 gene therapy delivering PPCA, with data presented for mouse Alzheimer’s models and non-human primates.
Key point: Amlogenyx reported preclinical results showing reduced amyloid burden across models and said AM805 is in IND-enabling studies.
Implication: Signals pipeline investment and modality expansion.
🩸 Roche wins CE mark for Elecsys ApoE4 blood test [6] [EU • 16 Mar 2026]
https://www.prnewswire.com/news-releases/roche-receives-ce-mark-for-first-ivd-immunoassay-blood-test-to-identify-carriers-of-apoe4-a-genetic-variant-present-in-up-to-60-of-patients-diagnosed-with-alzheimers-disease-302714082.html
Context: Roche positioned Elecsys ApoE4 as a blood-based IVD immunoassay to identify ApoE4 carrier status and integrate with other Alzheimer’s biomarkers.
Key point: Roche received CE mark for Elecsys ApoE4, which the company says is the first CE-marked IVD immunoassay blood test for ApoE4 carrier identification.
Implication: Could inform practice and payer discussions; interpretation depends on study design and confounding control.
💪 Atossa highlights (Z)-endoxifen data in Duchenne muscular dystrophy [7] [US • 12 Mar 2026]
https://investors.atossatherapeutics.com/2026-03-12-Atossa-Therapeutics-Presents-Clinical-Trial-Update-Highlighting-Z-Endoxifen-Research-at-the-2026-MDA-Clinical-Scientific-Conference
Context: Atossa presented findings from the mdx5Cv dystrophic mouse model at the 2026 MDA Clinical & Scientific Conference in Orlando, Florida.
Key point: Atossa reported that (Z)-endoxifen improved muscle performance and reduced muscle damage markers in a preclinical DMD model, with tolerability described as favorable.
Implication: Signals pipeline investment and modality expansion.
📘 NeuroSense PrimeC Phase 2b ALS results appear in JAMA Neurology [8] [US • 16 Mar 2026]
https://www.prnewswire.com/news-releases/jama-neurology-publishes-results-from-paradigm-phase-2b-trial-of-primec-in-als-demonstrating-meaningful-clinical-outcomes-and-biological-activity-302714793.html
Context: PARADIGM was a multinational, randomized, double-blind, placebo-controlled Phase 2b trial with a 6-month blinded period followed by a 12-month open-label extension.
Key point: NeuroSense said JAMA Neurology published PARADIGM results showing slower functional decline, reduced ALS-related complications, and biomarker changes with PrimeC.
Implication: May influence prescriber choice and payer reviews pending full data.
