India has entered a new era in neurological treatment with the launch of its first amyloid-targeting Alzheimer’s drug, Lormalzi (donanemab), by Eli Lilly and Company. The breakthrough therapy has been approved for patients with early-stage Alzheimer’s disease and mild cognitive impairment.
But the excitement comes with a massive price tag.
A single 350 mg vial of Lormalzi will cost ₹91,688 in India, making it one of the most expensive neurological therapies available in the country today.
Unlike traditional Alzheimer’s medicines that mainly manage symptoms, donanemab is designed to target the disease process itself.
The therapy works by removing amyloid plaques — protein deposits in the brain strongly associated with Alzheimer’s progression. Donanemab
The drug:
Clinical trials showed up to 35% slowing of disease progression in some early-stage patients over 18 months.
Globally, the drug is sold under the brand name Kisunla and received US FDA approval in 2024.
The launch comes at a time when India’s dementia crisis is growing fast.
According to reports:
India’s ageing population is expected to dramatically increase neurological disorders over the next decade.
The economic burden is already enormous:
Despite the medical breakthrough, experts say affordability may become the biggest obstacle.
At ₹91,688 per vial:
That means total treatment costs could potentially exceed ₹15-20 lakh for some patients.
Eli Lilly says it will launch an “Alternate Access Programme” to improve affordability for eligible patients.
However, experts believe access will still remain limited largely to affluent urban patients and premium hospitals.
Interestingly, the launch is also controversial.
A recent Cochrane review involving over 20,000 patients reportedly concluded that amyloid-targeting drugs like donanemab produced “absent or trivial” clinical benefits despite reducing plaque buildup.
Researchers also raised concerns about side effects including:
However, Eli Lilly strongly rejected the review’s conclusions, arguing that approved drugs should not be grouped with failed experimental molecules.
This debate is now becoming one of the biggest controversies in modern neurology:
Does removing amyloid plaques actually translate into meaningful real-world cognitive improvement?
Despite the debate, the launch is historically significant.
India now joins a small group of countries offering advanced disease-modifying Alzheimer’s therapies commercially.
The move could:
But it also exposes a major healthcare reality:
India is entering an era where breakthrough medicines exist — but many remain financially inaccessible to most patients.
The bigger question now is not only whether Alzheimer’s can finally be slowed, but whether India’s healthcare system can make such cutting-edge therapies accessible beyond a tiny elite population.
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