Delix Therapeutics
reported positive efficacy data for its lead non-hallucinogenic psychoplastogen DLX-001 (zalsupindole) in October 2025, alongside FDA clearance of a Phase II trial design featuring at-home administration rather than clinic-based supervised dosing.
- Country
- United States
non-hallucinogenic
us
Coverage
| CN | EU | US | |
|---|---|---|---|
| therapeutics-platforms | ✓ | ✓ | ✓ |
Regulatorsfdaemanmpa
Technologies
| Name | Cluster | Risk | |
|---|---|---|---|
| Psychedelic medicine & neuropsychiatric biologics | therapeutics-platforms | High | → |
Compiled by BIOECON via the bioecon-brief pipeline.
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