Wynne, Chris
Lorch, Ulrike
Krantz, Edrich
Katial, Rohit
Ashdown, Thomas
Luque, Monica
Sattar, Abid
Rai, Masna
Vashishta, Laxmikant
Petrovic, Katarina
Ruffieux, Ruth
Leutz, Steffen
Berti, Fausto
Clinical trials referenced in this document:
Documents that mention this clinical trial
Pharmacokinetic Similarity of Biosimiliar AVT05 Versus Reference Product Golimumab in Healthy Adults: A Double-Blind, Three-Arm, Parallel-Group Study
https://doi.org/10.1007/s40259-025-00749-7
Funding for this research was provided by:
Alvotech Swiss AG
Article History
Accepted: 9 October 2025
First Online: 10 November 2025
Declarations
:
: Chris Wynne is an employee of, and hold shares in, New Zealand Clinical Research that received payment for carrying out the study. Ulrike Lorch and Thomas Ashdown are employees of Richmond Pharmacology Ltd that received payment for carrying out the study. Edrich Krantz is an employee of Farmovs Integrated Research Solutions that received payment for carrying out the study. Rohit Katial is an employee of New Zealand Clinical Research that received payment for carrying out the study. Monica Luque, Abid Sattar, Masna Rai, Laxmikant Vashishta, Ruth Ruffieux, Steffen Leutz, and Fausto Berti are employees at Alvotech. Katarina Petrovic was an employee of Alvotech at the time of the study.
: The study was conducted in accordance with the Declaration of Helsinki, the International Council for Harmonisation Good Clinical Practice guidelines, and the appropriate regulatory requirements in the countries in which the study was conducted. The protocol, its amendments, and informed consent documentation were reviewed and approved by the institutional review board(s) or independent ethics committee(s) at each study site.
: All participants gave written informed consent to participate in the study prior to undertaking any study-related examination or activity. The informed consent document was approved by each study site’s institutional review board or independent ethics committee.
: Not applicable.
: The datasets generated and/or analyzed during the current study are available from the sponsor on reasonable request.
: Not applicable.
: All authors were involved in the conception and design of the study. CW, UL, EK, RK, TA, and RR were involved in the provision of study materials and patients and acquisition of the data. CW, UL, EK, RK, TA, ML, AS, MS, LV, SL, and FB performed the analysis and/or the interpretation of the data. All authors revised the report critically. All authors approved the final version.