Lyndra’s long-acting risperidone formulation hits PhIII schizophrenia trial endpoints
Lyndra Therapeutics’ schizophrenia drug candidate has passed its late-stage clinical test according to interim data, prompting an early end to the study and preparations for a registrational safety trial.
The Phase III STARLYNG-1 trial was designed to test once-weekly LYN-005 against standard of care daily Risperdal in 90 people with schizophrenia or schizoaffective disorder. LYN-005 contains the same active ingredient as Risperdal — risperidone — but was designed for once-weekly dosing using Lyndra’s LYNX drug delivery platform
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