Rehberg, Sebastian
Borgstedt, Rainer
Frank, Sandra
Černý, Vladimír
Sus, Jan https://orcid.org/0009-0003-9832-6526
Unger, Martin
Klade, Christoph
Krejcy, Kurt
Kirchbaumer-Baroian, Nairi
Bouvet, Olivier
Krumpl, Günther
Duška, František
,
Funding for this research was provided by:
AOP Health
Article History
Received: 7 October 2025
Accepted: 17 March 2026
First Online: 1 April 2026
Declarations
:
: Jan Sus, Martin Unger, Christoph Klade, Kurt Krejcy, Nairi Kirchbaumer-Baroian, and Olivier Bouvet are employees of AOP Orphan Pharmaceuticals GmbH. Günther Krumpl is a Board Director of AOP Health International Management AG.
: The data that support the findings of this study are openly available in EU Clinical Trials Register at , EudraCT Number: 2017-002138-22.
: The trial protocol was approved by the responsible ethics committees: in Germany (reference no.FF 06/17n; approval date 01 April 2020) and in the Czech Republic (reference no. 202002 I49M; approval date 6February 2020).
: Written informed consent was obtained from all patients or their legal representativesprior to any interventions. Additionally, specifi c informed consent was required for participation in the sub-study.
: The manuscript contains only anonymized, aggregated data and does not include anypersonally identifi able participant information; therefore, consent for publication is not applicable.
: As this PK sub-study included only patients who received landiolol, the randomization code isnot applicable.