Open Access
Hepatotoxicity of AKR1C3 Inhibitor BAY1128688: Findings from an Early Terminated Phase IIa Trial for the Treatment of Endometriosis
Jan Hilpert
1
,
Esther Groettrup-Wolfers
1
,
Hristiyan Kosturski
2
,
LAURA BENNETT
3
,
Catriona L K Barnes
3
,
Kerstin Gude
1
,
Isabella Gashaw
1
,
Stefanie Reif
1
,
Thomas Steger-Hartmann
1
,
Christian Scheerans
1
,
Alexander Solms
1
,
Antje Rottmann
1
,
Guangping Mao
1
,
Charles Chapron
4
1
Pharmaceuticals, Bayer AG, Berlin, Germany
|
2
Svelte® scientific GmbH, Berlin, Germany
|
3
Fios Genomics Ltd, Edinburgh, UK
|
Publication type: Journal Article
Publication date: 2023-07-09
scimago Q2
wos Q3
SJR: 0.691
CiteScore: 4.1
Impact factor: 2.1
ISSN: 11745886, 11796901
PubMed ID:
37422772
Pharmacology
Abstract
BAY1128688 is a selective inhibitor of aldo-keto reductase family 1 member C3 (AKR1C3), an enzyme implicated in the pathology of endometriosis and other disorders. In vivo animal studies suggested a potential therapeutic application of BAY1128688 in treating endometriosis. Early clinical studies in healthy volunteers supported the start of phase IIa. This manuscript reports the results of a clinical trial (AKRENDO1) assessing the effects of BAY1128688 in adult premenopausal women with endometriosis-related pain symptoms over a 12-week treatment period. Participants in this placebo-controlled, multicenter phase IIa clinical trial (NCT03373422) were randomized into one of five BAY1128688 treatment groups: 3 mg once daily (OD), 10 mg OD, 30 mg OD, 30 mg twice daily (BID), 60 mg BID; or a placebo group. The efficacy, safety, and tolerability of BAY1128688 were investigated. Dose-/exposure-dependent hepatotoxicity was observed following BAY1128688 treatment, characterized by elevations in serum alanine transferase (ALT) occurring at around 12 weeks of treatment and prompting premature trial termination. The reduced number of valid trial completers precludes conclusions regarding treatment efficacy. The pharmacokinetics and pharmacodynamics of BAY1128688 among participants with endometriosis were comparable with those previously found in healthy volunteers and were not predictive of the subsequent ALT elevations observed. The hepatotoxicity of BAY1128688 observed in AKRENDO1 was not predicted by animal studies nor by studies in healthy volunteers. However, in vitro interactions of BAY1128688 with bile salt transporters indicated a potential risk factor for hepatotoxicity at higher doses. This highlights the importance of in vitro mechanistic and transporter interaction studies in the assessment of hepatoxicity risk and suggests further mechanistic understanding is required. NCT03373422 (date registered: November 23, 2017)
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GOST
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Hilpert J. et al. Hepatotoxicity of AKR1C3 Inhibitor BAY1128688: Findings from an Early Terminated Phase IIa Trial for the Treatment of Endometriosis // Drugs in R and D. 2023. Vol. 23. No. 3. pp. 221-237.
GOST all authors (up to 50)
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Hilpert J., Groettrup-Wolfers E., Kosturski H., BENNETT L., Barnes C. L. K., Gude K., Gashaw I., Reif S., Steger-Hartmann T., Scheerans C., Solms A., Rottmann A., Mao G., Chapron C. Hepatotoxicity of AKR1C3 Inhibitor BAY1128688: Findings from an Early Terminated Phase IIa Trial for the Treatment of Endometriosis // Drugs in R and D. 2023. Vol. 23. No. 3. pp. 221-237.
Cite this
RIS
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TY - JOUR
DO - 10.1007/s40268-023-00427-5
UR - https://doi.org/10.1007/s40268-023-00427-5
TI - Hepatotoxicity of AKR1C3 Inhibitor BAY1128688: Findings from an Early Terminated Phase IIa Trial for the Treatment of Endometriosis
T2 - Drugs in R and D
AU - Hilpert, Jan
AU - Groettrup-Wolfers, Esther
AU - Kosturski, Hristiyan
AU - BENNETT, LAURA
AU - Barnes, Catriona L K
AU - Gude, Kerstin
AU - Gashaw, Isabella
AU - Reif, Stefanie
AU - Steger-Hartmann, Thomas
AU - Scheerans, Christian
AU - Solms, Alexander
AU - Rottmann, Antje
AU - Mao, Guangping
AU - Chapron, Charles
PY - 2023
DA - 2023/07/09
PB - Springer Nature
SP - 221-237
IS - 3
VL - 23
PMID - 37422772
SN - 1174-5886
SN - 1179-6901
ER -
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BibTex (up to 50 authors)
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@article{2023_Hilpert,
author = {Jan Hilpert and Esther Groettrup-Wolfers and Hristiyan Kosturski and LAURA BENNETT and Catriona L K Barnes and Kerstin Gude and Isabella Gashaw and Stefanie Reif and Thomas Steger-Hartmann and Christian Scheerans and Alexander Solms and Antje Rottmann and Guangping Mao and Charles Chapron},
title = {Hepatotoxicity of AKR1C3 Inhibitor BAY1128688: Findings from an Early Terminated Phase IIa Trial for the Treatment of Endometriosis},
journal = {Drugs in R and D},
year = {2023},
volume = {23},
publisher = {Springer Nature},
month = {jul},
url = {https://doi.org/10.1007/s40268-023-00427-5},
number = {3},
pages = {221--237},
doi = {10.1007/s40268-023-00427-5}
}
Cite this
MLA
Copy
Hilpert, Jan, et al. “Hepatotoxicity of AKR1C3 Inhibitor BAY1128688: Findings from an Early Terminated Phase IIa Trial for the Treatment of Endometriosis.” Drugs in R and D, vol. 23, no. 3, Jul. 2023, pp. 221-237. https://doi.org/10.1007/s40268-023-00427-5.