Cherniakov, Irina https://orcid.org/0009-0002-2369-2858
Wagner, Avia Merenlender
Eshet, Roy
Tiver, Ryan
Bibi, David
Perlstein, Itay https://orcid.org/0000-0001-8700-3957
Kalmanczhelyi, Attila
Sharon, Nir
Cohen, Gadi
Ferderber, Kristina
Roberts, James
Elgart, Anna
Gutman, Dikla
Rabinovich-Guilatt, Laura
Clinical trials referenced in this document:
Documents that mention this clinical trial
Safety, Tolerability, and Pharmacokinetics of Subcutaneous Extended-Release Injectable Olanzapine in Patients with Schizophrenia and Schizoaffective Disorder
https://doi.org/10.1007/s40261-025-01507-x
Funding for this research was provided by:
Teva Branded Pharmaceutical Products R&D LLC
Article History
Received: 21 May 2025
Accepted: 4 November 2025
First Online: 3 February 2026
Declarations
:
: Irina Cherniakov, Roy Eshet, Ryan Tiver, David Bibi, Attila Kalmanczhelyi, Nir Sharon, Gadi Cohen, and James Roberts are Teva employees. Avia Merenlender Wagner, Kristina Ferderber, Anna Elgart, Dikla Gutman, and Laura Rabinovich-Guilatt are Teva employees and shareholders. Itay Perlstein is a Magic Wand Research employee and a consultant for Teva.
: This study was conducted in accordance with current ICH-Good Clinical Practice guidelines, the Declaration of Helsinki, and any conditions required by regulatory authorities and institutional review boards (IRBs) that approved the study protocol. The study protocol received IRB approval before trial initiation (IRB approval number: Pro00041955).
: Informed consent was obtained from all individual participants included in the study.
: Not applicable.
: Qualified researchers may request access to patient-level data and related study documents, including the study protocol and the statistical analysis plan. Requests will be assessed for scientific merit, product approval status, and conflicts of interest. If the request is approved, patient-level data will be de-identified and study documents will be redacted to protect the privacy of trial participants and to protect commercially confidential information. Please e-mail USMedInfo@tevapharm.com to make your request.
: Not applicable.
: All authors participated in data interpretation and drafting the article or revising it critically for important intellectual content. Study conception and design were performed by IC, AMW, RE, IP, NS, GC, KF, JR, AE, and LR-G. Acquisition of data was performed by AMW, RT, IP, and AK. Data analysis was performed by IC, AMW, RE, DB, IP, NS, GC, and DG. All authors approved the final version to be published.