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| Funder | Wellcome Trust |
|---|---|
| Recipient Organization | Alto Neuroscience |
| Country | United Kingdom |
| Start Date | Jul 24, 2024 |
| End Date | Oct 23, 2026 |
| Duration | 821 days |
| Number of Grantees | 1 |
| Roles | Award Holder |
| Data Source | Europe PMC |
| Grant ID | 306439 |
Bipolar disorder is a severe, life-long psychiatric condition associated with a high burden of disability and risk of suicide.
The only approved treatments for its depressive phase (BD-D) are antipsychotic medications, which carry many side effects.
As BD-D is defined by clinical phenomenology rather than by biology, successful development of new treatment options will most likely come by targeting biologically defined patient subgroups characterized by relevant pathophysiology (i.e. a precision psychiatry approach).
Extensive data show neuroplasticity-related abnormalities in the brains of BD-D patients that can be clinically identified as deficits in memory, commonly seen in BD-D.
A drug that enhances hippocampal neuroplasticity therefore holds promise specifically for memory-impaired BD-D patients. ALTO-100 is an orally active small molecule with a novel pro-neurogenesis/neuroplasticity mechanism of action. We have shown that MDD or PTSD patients with poor memory respond better to ALTO-100 than those with intact cognition.
Here, we propose taking a precision psychiatry approach through a poor memory-stratified Phase 2b trial of ALTO-100 in BD-D, following closely the already FDA-tested design of a recently launched MDD Phase 2b.
A successful outcome would accelerate this drug into Phase 3, potentially providing a groundbreaking new option for a highly underserved clinical population.
Alto Neuroscience
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