Safety, Tolerability, and Pharmacokinetics of Subcutaneous Extended-Release Injectable Olanzapine in Patients with Schizophrenia and Schizoaffective Disorder
TV-44749 administration resulted in a sustained release profile and comparable exposure to daily therapeutic doses of oral olanzapine over a monthly dosing interval. The TV-44749 systemic safety profile was consistent with approved oral olanzapine. The local tolerability was acceptable, and there were no PDSS events. These results contributed to the dose selection of TV-44749 in a phase III study evaluating its efficacy and safety in adults with schizophrenia (SOLARIS; NCT05693935).
Authors
- Attila Kalmanczhelyi
- Roy Eshet
- Irina Cherniakov
- Anna Elgart
- Kristina Ferderber
- Itay Perlstein
- Dikla Gutman
- Ryan Tiver
- David Bibi
- Nir Adam Sharon
- Avia Merenlender Wagner
- Laura Rabinovich-Guilatt
- Gadi Cohen
- James Roberts
Institutions
- Norton Healthcare (US)
- Pliva (Croatia) (HR)
- Teva Pharmaceuticals (Israel) (IL)
- Teva Pharmaceuticals (United States) (US)
- Teva Pharmaceuticals (Hungary) (HU)
Publication Details
- Journal
- Clinical Drug Investigation
- Published
- 2026-02-03
- DOI
- https://doi.org/10.1007/s40261-025-01507-x
- Primary Topic
- Schizophrenia research and treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Teva Pharmaceutical Industries