UCI Health launches world's first embryonic stem cell trial for Huntington's disease
· News-MedicalUCI Health, the clinical enterprise of the University of California, Irvine, has opened the world's first in-human embryonic stem cell-derived clinical trial for Huntington's disease.
The phase 1b/2a trial will evaluate the safety of hNSC-01 neural stem cells derived from embryonic stem cells which are precisely delivered to the brain by a specialized neurological mapping and targeting stereotactic system and performed in an MRI suite.
The trial is the result of many years of basic and translational science carried out at UCI, and funding by the California Institute of Regenerative Medicine (CIRM), to the research team led by Leslie M. Thompson, Ph.D., Donald Bren Professor of psychiatry and human behavior, as well as neurobiology and behavior, at UC Irvine.
"This clinical trial highlights the important role that an interdisciplinary academic and clinical team together with the HD families, plays in advancing medicine," said Dr. Thompson, who is the clinical trial sponsor. "We are grateful to our patients and their incredible families for their bravery to provide hope for others with very few options."
The first patient received the intervention at UCI Health –– Irvine, home to Orange County's first adult bone marrow/stem cell transplant and cellular therapy program, in May. UCI Health neurosurgeon Dr. Jefferson W. Chen, assisted by a team including a neurosurgery fellow, delivered the intervention. A second patient is scheduled to receive the intervention in July.
Dr. Ravi Rajmohan, UCI Health neurologist, clinical trial's principal investigatorThe first patient intervention went very well. To date, they haven't reported any serious adverse events. This trial may help us move one step closer to a future with available treatments that could potentially slow the progression of Huntington's disease."
What intervention is being tested?
- Protect existing brain cells
- Replace lost cells
- Rebuild impaired brain circuits
- Release helpful proteins, such as brain-derived neurotrophic factor (BDNF)
- Reduce harmful protein accumulations that damage brain cells
The stem cells were also shown to be safe over long periods in mice.
How is the intervention delivered?
The stem cells are implanted during a roughly six-hour surgical procedure done under general anesthesia. While lying face down in an MRI scanner, the patient receives stem cells implanted directly into the striatum deep in the brain, using a purchased proprietary therapy-enabling platform for navigation and delivery. Damage to the striatum, which is responsible for motor control, decision-making, motivation and more, causes Huntington's disease symptoms.
Subjects will be closely monitored for safety as well as preliminary signs of potential benefit.
How is the clinical trial funded?
How many people will the trial enroll?
The clinical trial will enroll 21 people ages 18 to 65 with early-stage Huntington's disease. Twelve participants will be enrolled into a phase 1b dose-escalation group and nine in a phase 2a expansion group.
How does Huntington's disease impact patients and families?
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