×

US FDA approves Lantheus’ brain-imaging agent for Alzheimer’s assessment

By Thomson Reuters Aug 14, 2026 | 7:19 AM

Aug 14 (Reuters) – The U.S. Food and Drug Administration has approved a radioactive agent from Lantheus Holdings for use in brain scans to help assess patients for Alzheimer’s disease, ​the company said on Friday.

The agent, branded as Tauklarify, ‌is injected before a positron emission tomography, or PET, scan. It makes abnormal deposits of tau proteins linked to Alzheimer’s visible in images of the brain in adults with cognitive impairment who are being assessed for the disease.

A positive ‌scan ​does not necessarily confirm tau pathology, while ⁠a negative scan does not ⁠rule it out, the company said.

The approval was supported by two studies in which independent readers assessed Tauklarify PET scans from more than 500 participants and classified them as positive or ​negative for tau pathology.

More than 7 million people in the United States have Alzheimer’s, and the number of people aged 65 ⁠or older with the disease could exceed ⁠13 million by 2050, Lantheus said.

Tauklarify will compete ​with Eli Lilly’s Tauvid, which was approved in 2020 for use with ​PET scans to estimate the amount and distribution of ‌tau deposits in adults being assessed for Alzheimer’s disease.

Alzheimer’s is a progressive brain disease and the most common cause of dementia, gradually damaging memory, thinking and the ability to perform everyday tasks. It is ⁠associated with abnormal deposits of beta-amyloid and tau proteins in the brain.

Amyloid can begin accumulating years before symptoms appear, while the amount and spread ⁠of tau are ‌more closely linked to worsening memory and thinking ⁠problems.

The approval expands Lantheus’ Alzheimer’s imaging portfolio by ​adding a ‌tau-targeting agent alongside Neuraceq, its approved amyloid imaging ​agent.

Earlier this ⁠month, privately-held radiopharmaceutical company Curium agreed to buy Lantheus in a deal valued at up to $8 billion to expand its diagnostic and therapeutic radiopharmaceutical business. The transaction is expected to close in the first half of 2027.

(Reporting by Kunal Das and Puyaan Singh in Bengaluru; Editing ​by Devika Syamnath)