Company statement on expected drug interactions
NOVA-1 protocol: prohibited CYP2D6 inhibitors and CYP3A4 inhibitors and inducers
NOVA-1 protocol: prohibited antipsychotics and other psychotropic medications
“Patients who are currently taking oral antipsychotic medications, monoamine oxidase inhibitors (MAOIs), anticonvulsants (e.g., lamotrigine, Depakote), tricyclic antidepressants (e.g., imipramine, desipramine), selective serotonin reuptake inhibitors, and any other antidepressants or any other psychoactive medications (except lorazepam, zolpidem, zaleplon, eszopiclone, or similar benzodiazepines, diphenhydramine, benztropine, and propranolol).” (opens the source at this quote in a new tab)
Alcohol, cannabis, and smoking
Class context: metabolism and transport of amisulpride
“In vitro, amisulpride was not a substrate of CYP1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP2E1 and CYP3A4.” (opens the source at this quote in a new tab)
“Amisulpride is a substrate for P-gp, BCRP, OCT1, MATE1 and MATE2-K, but not a substrate for OATP1B1, OATP1B3, OAT1, OAT3 and OCT2.” (opens the source at this quote in a new tab)
“No clinical drug interaction trials have been conducted with BARHEMSYS.” (opens the source at this quote in a new tab)
Class context: QT-prolonging drugs in amisulpride labeling
Clinical drug interaction studies with LB-102
No evidence found.
In vitro CYP and transporter substrate findings for LB-102
No evidence found.
Restrictions on QT-prolonging medications in the LB-102 trial protocols
No evidence found.