Eli Lilly Neuroscience Chief Anne White to Retire After Leading Alzheimer's Drug Launch
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Eli Lilly announced that Anne White (search), head of its neuroscience division, will retire in December after a 30-year career at the company.
White oversaw the regulatory submission and launch of Kisunla, Lilly's Alzheimer's drug that represents the culmination of decades of research into treatments for the memory-robbing condition.
The company is searching for internal and external candidates to replace White, who previously led Lilly's oncology unit and helped integrate the Loxo Oncology (search) acquisition.
Eli Lilly announced Wednesday that Anne White (search), head of its neuroscience division, will retire in December after a 30-year career at the Indianapolis pharmaceutical company. The company is now searching for internal and external candidates to replace White, who will step down on December 31.
White, who serves on Lilly's executive committee, took over neuroscience leadership in 2021 when the company split its biomedicines unit in two to prepare for expected launches of immune system and Alzheimer's disease (search) drugs. Previously, she led Lilly's oncology unit and helped oversee the successful acquisition and integration of Loxo Oncology (search), which became the foundation for the company's current cancer drug efforts.
"Anne's career has been defined by a deep commitment to advancing medicines for some of the most challenging diseases affecting patients globally," Lilly CEO David Ricks said in a statement.
Kisunla Launch Marks Career Achievement
As head of Lilly Neuroscience, White oversaw the regulatory submission and launch of Kisunla, a drug designed to slow the progression of Alzheimer's disease (search). For Lilly, the U.S. approval was the culmination of decades of research into drugs for the memory-robbing condition — work that, until Kisunla, had repeatedly come up short.
The achievement was personal for White, who has written about her mother's experience with Alzheimer's and how she hopes recent research advances will lead to improved treatment and care. "The progress we are now realizing will lead to more investment and research in Alzheimer's disease (search) that will unlock further understanding and open the door to address other neurodegenerative conditions," she wrote in a Fortune editorial published the day of Kisunla's FDA clearance. "This moment will be a catalyst to drive progress toward understanding diseases such as ALS (search), Parkinson's (search), and multiple sclerosis (search)."
Addressing Safety Concerns and Market Performance
Lilly recently won Food and Drug Administration clearance for modified dosing of Kisunla aimed at reducing a potentially dangerous side effect known as "ARIA," which has been a significant concern for Kisunla and other drugs that work similarly, like Eisai and Biogen's Leqembi.
While analysts expect Kisunla will eventually become a blockbuster, it has performed modestly since launching last year. Lilly recorded $49 million in sales from the drug during the three-month period from April through June.
Expanding Neuroscience Pipeline
Lilly is developing another Alzheimer's medicine, remternetug, that's currently in Phase 3 testing. The company's neuroscience pipeline also includes a handful of gene therapies for diseases like Parkinson's (search), Gaucher (search) and frontotemporal dementia (search), as well as four drugs for pain. Lilly recently added one of those pain therapies via its acquisition of the California-based startup SiteOne Therapeutics (search).
In its statement, Lilly credited White with efforts to speed drug development timelines across the company during her tenure.