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To Steer a Brain in Real Time, You May Not Need to Model It

Romeo Kuok October 15, 2026October 15, 2026

NeuroAI Needs a Definition Before It Needs a Budget

Martin Kardzhilov October 15, 2026October 15, 2026

The Humanoid Industry Has a Capacity Problem It Cannot Announce Away

Martin Kardzhilov October 15, 2026October 15, 2026

Neuro AI’s Best Annotator Is the Person Whose Brain It Is

Ralph Sun October 14, 2026October 14, 2026

Neuro AI Has a Labelling Problem, Not a Compute Problem

Ralph Sun October 14, 2026October 14, 2026

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Neuroscience

To Steer a Brain in Real Time, You May Not Need to Model It

Closed-loop stimulation has been framed as a modelling problem — understand the dynamics well enough…

Romeo Kuok October 15, 2026October 15, 2026
Neuroscience

NeuroAI Needs a Definition Before It Needs a Budget

NeuroAI is used to describe everything from brain-inspired chip design to neural decoding. Until the…

Martin Kardzhilov October 15, 2026October 15, 2026
Robotics

The Humanoid Industry Has a Capacity Problem It Cannot Announce Away

Announced production capacity now runs an order of magnitude ahead of units doing paid work.…

Martin Kardzhilov October 15, 2026October 15, 2026

Editor Choice

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Neuroscience

To Steer a Brain in Real Time, You May Not Need to Model It

Romeo Kuok October 15, 2026October 15, 2026
Neuroscience

NeuroAI Needs a Definition Before It Needs a Budget

Martin Kardzhilov October 15, 2026October 15, 2026
FDA’s Ziihera Approval Creates a New First-Line HER2-Positive GEA Decision Tree
Biotechnology

FDA’s Ziihera Approval Creates a New First-Line HER2-Positive GEA Decision Tree

Jane AubreyAugust 27, 2026August 27, 2026

FDA has approved two zanidatamab-hrii, or Ziihera, treatment approaches for adults with unresectable locally advanced or metastatic HER2-positive gastric, gastroesophageal-junction…

Capricor’s PDUFA Extension Makes the Endpoint Case Central to Deramiocel’s Review
Biotechnology

Capricor’s PDUFA Extension Makes the Endpoint Case Central to Deramiocel’s Review

Jane AubreyAugust 25, 2026August 25, 2026

Capricor Therapeutics announced on August 24 that FDA extended the target action date for its Biologics License Application for deramiocel,…

Genglycos Brings the First Approved Therapy to GSDIa—But Its Accelerated Approval Is Only the Beginning
Genetics

Genglycos Brings the First Approved Therapy to GSDIa—But Its Accelerated Approval Is Only the Beginning

Jane AubreyAugust 21, 2026August 21, 2026

The FDA’s accelerated approval of Genglycos is a landmark for patients with glycogen storage disease type Ia, a rare inherited…

FDA Feedback Gives Oncolytics a Potential Shortcut—But REO 033 Still Must Earn Its Pivotal Expansion
Biotechnology

FDA Feedback Gives Oncolytics a Potential Shortcut—But REO 033 Still Must Earn Its Pivotal Expansion

Jane AubreyAugust 20, 2026August 20, 2026

Oncolytics Biotech has secured FDA written feedback that could make the development path for pelareorep in metastatic colorectal cancer more…

Argenx’s ALKIVIA Result Opens a New Therapeutic Front in Autoimmune Myositis
Biotechnology

Argenx’s ALKIVIA Result Opens a New Therapeutic Front in Autoimmune Myositis

Marcus ChenAugust 18, 2026

Argenx has reported positive Phase 3 results for VYVGART Hytrulo in autoimmune myositis, a heterogeneous group of rare inflammatory diseases…

How BioLayer is Rewriting the Data Supply Chain for Healthcare AI
Biotechnology

How BioLayer is Rewriting the Data Supply Chain for Healthcare AI

Jane AubreyAugust 18, 2026August 18, 2026

As consumer health agents and biomedical AI models accelerate, the central economic and ethical question facing the industry is no…

AbelZeta’s Prizlon-cel IND Reopens the Question of How CAR-T Can Work After CAR-T Failure
Biotechnology

AbelZeta’s Prizlon-cel IND Reopens the Question of How CAR-T Can Work After CAR-T Failure

Jane AubreyAugust 17, 2026August 17, 2026

AbelZeta Pharma has received FDA clearance to begin U.S. clinical development of Prizlon-cel, an anti-CD20/CD19 bispecific CAR-T therapy for relapsed…

Zenbexus Opens a New Myeloma Drug Class, but the Confirmatory Test Still Lies Ahead
Pharma

Zenbexus Opens a New Myeloma Drug Class, but the Confirmatory Test Still Lies Ahead

Jane AubreyAugust 14, 2026August 14, 2026

The FDA’s accelerated approval of Bristol Myers Squibb’s Zenbexus gives multiple-myeloma treatment a new class of medicine and creates an…

Xilio’s New IND Tests Whether Masked IL-2 Can Make Immunotherapy Safer in Solid Tumors
Biotechnology

Xilio’s New IND Tests Whether Masked IL-2 Can Make Immunotherapy Safer in Solid Tumors

biotechcodexAugust 13, 2026August 13, 2026

The U.S. Food and Drug Administration has cleared Xilio Therapeutics to begin human testing of XTX501, a bispecific PD-1 and…

Manufacturing Stumble: FDA Rejects ITM Radiopharma’s Neuroendocrine Tumor Therapy
Genetics

Manufacturing Stumble: FDA Rejects ITM Radiopharma’s Neuroendocrine Tumor Therapy

Jane AubreyAugust 11, 2026August 11, 2026

In a stark reminder of the immense logistical complexities surrounding radiopharmaceuticals, the U.S. Food and Drug Administration (FDA) has issued…

Eli Lilly Escalates Obesity War, Offers Early Access to Next-Gen GLP-1 Retatrutide
Lifestyle

Eli Lilly Escalates Obesity War, Offers Early Access to Next-Gen GLP-1 Retatrutide

Jane AubreyAugust 10, 2026August 10, 2026

The battle for dominance in the lucrative obesity drug market is entering a new and aggressive phase. Eli Lilly has…

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