Cargando…

First‐in‐human trial to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of STR‐324, a dual enkephalinase inhibitor for pain management

AIM: Dual enkephalinase inhibitors (DENKIs) are involved in the regulation of nociception via opioid receptors. The novel compound STR‐324 belongs to the DENKI pharmacological class. This first‐in‐human study evaluated the safety, tolerability, pharmacokinetics and pharmacodynamics of STR‐324 in hea...

Descripción completa

Detalles Bibliográficos
Autores principales: Moss, Laurence M., Berends, Cecile L., van Brummelen, Emilie M. J., Kamerling, Ingrid M. C., Klaassen, Erica S., Bergmann, Kirsten, Ville, Vanessa, Juarez‐Perez, Victor, Benichou, Annie‐Claude, Groeneveld, Geert Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292820/
https://www.ncbi.nlm.nih.gov/pubmed/34046921
http://dx.doi.org/10.1111/bcp.14931
_version_ 1784749468314238976
author Moss, Laurence M.
Berends, Cecile L.
van Brummelen, Emilie M. J.
Kamerling, Ingrid M. C.
Klaassen, Erica S.
Bergmann, Kirsten
Ville, Vanessa
Juarez‐Perez, Victor
Benichou, Annie‐Claude
Groeneveld, Geert Jan
author_facet Moss, Laurence M.
Berends, Cecile L.
van Brummelen, Emilie M. J.
Kamerling, Ingrid M. C.
Klaassen, Erica S.
Bergmann, Kirsten
Ville, Vanessa
Juarez‐Perez, Victor
Benichou, Annie‐Claude
Groeneveld, Geert Jan
author_sort Moss, Laurence M.
collection PubMed
description AIM: Dual enkephalinase inhibitors (DENKIs) are involved in the regulation of nociception via opioid receptors. The novel compound STR‐324 belongs to the DENKI pharmacological class. This first‐in‐human study evaluated the safety, tolerability, pharmacokinetics and pharmacodynamics of STR‐324 in healthy male participants. METHODS: This was a randomised, double‐blind, placebo‐controlled ascending dosing study in two parts: in part 1, 30 participants received 0.004‐11.475 mg h(−1) of STR‐324 or placebo (ratio 4:1) by 4 h intravenous infusion in a two‐group, partial crossover design with four treatment periods separated by 1 month wash‐out, and in part 2, 48 participants divided into three groups received either the active drug (1.25‐11.25 mg h(−1)) or placebo (ratio 3:1) by 48 h intravenous infusion. Safety and tolerability parameters, pharmacokinetics and pharmacodynamic effects on neurocognitive and neurophysiological tasks and on a nociceptive test battery were evaluated. RESULTS: No clinically relevant changes in safety parameters were observed. All treatment‐emergent adverse events were mild and transient. The pharmacokinetics of STR‐324 could not be determined due to most concentrations being below quantifiable limits. STR‐324 metabolite concentrations were measurable, showing dose proportionality of C (max) and AUC(inf) with an estimated t (1/2) of 0.2‐0.5 h. Significant changes in pharmacodynamic parameters were observed, but these were not consistent or dose‐dependent. CONCLUSION: STR‐324 displayed favourable safety and tolerability profiles at all doses up to 11.475 mg h(−1). Although pharmacokinetic characterisation of STR‐324 was limited, dose proportionality could be assumed based on major metabolite data assayed as proxy. No clear effects on nociceptive thresholds or other pharmacodynamic measures were observed. Trial registry: EudraCT (2014‐002402‐21) and toetsingonline.nl (63085).
format Online
Article
Text
id pubmed-9292820
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-92928202022-07-20 First‐in‐human trial to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of STR‐324, a dual enkephalinase inhibitor for pain management Moss, Laurence M. Berends, Cecile L. van Brummelen, Emilie M. J. Kamerling, Ingrid M. C. Klaassen, Erica S. Bergmann, Kirsten Ville, Vanessa Juarez‐Perez, Victor Benichou, Annie‐Claude Groeneveld, Geert Jan Br J Clin Pharmacol Original Articles AIM: Dual enkephalinase inhibitors (DENKIs) are involved in the regulation of nociception via opioid receptors. The novel compound STR‐324 belongs to the DENKI pharmacological class. This first‐in‐human study evaluated the safety, tolerability, pharmacokinetics and pharmacodynamics of STR‐324 in healthy male participants. METHODS: This was a randomised, double‐blind, placebo‐controlled ascending dosing study in two parts: in part 1, 30 participants received 0.004‐11.475 mg h(−1) of STR‐324 or placebo (ratio 4:1) by 4 h intravenous infusion in a two‐group, partial crossover design with four treatment periods separated by 1 month wash‐out, and in part 2, 48 participants divided into three groups received either the active drug (1.25‐11.25 mg h(−1)) or placebo (ratio 3:1) by 48 h intravenous infusion. Safety and tolerability parameters, pharmacokinetics and pharmacodynamic effects on neurocognitive and neurophysiological tasks and on a nociceptive test battery were evaluated. RESULTS: No clinically relevant changes in safety parameters were observed. All treatment‐emergent adverse events were mild and transient. The pharmacokinetics of STR‐324 could not be determined due to most concentrations being below quantifiable limits. STR‐324 metabolite concentrations were measurable, showing dose proportionality of C (max) and AUC(inf) with an estimated t (1/2) of 0.2‐0.5 h. Significant changes in pharmacodynamic parameters were observed, but these were not consistent or dose‐dependent. CONCLUSION: STR‐324 displayed favourable safety and tolerability profiles at all doses up to 11.475 mg h(−1). Although pharmacokinetic characterisation of STR‐324 was limited, dose proportionality could be assumed based on major metabolite data assayed as proxy. No clear effects on nociceptive thresholds or other pharmacodynamic measures were observed. Trial registry: EudraCT (2014‐002402‐21) and toetsingonline.nl (63085). John Wiley and Sons Inc. 2021-07-16 2022-01 /pmc/articles/PMC9292820/ /pubmed/34046921 http://dx.doi.org/10.1111/bcp.14931 Text en © 2021 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Moss, Laurence M.
Berends, Cecile L.
van Brummelen, Emilie M. J.
Kamerling, Ingrid M. C.
Klaassen, Erica S.
Bergmann, Kirsten
Ville, Vanessa
Juarez‐Perez, Victor
Benichou, Annie‐Claude
Groeneveld, Geert Jan
First‐in‐human trial to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of STR‐324, a dual enkephalinase inhibitor for pain management
title First‐in‐human trial to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of STR‐324, a dual enkephalinase inhibitor for pain management
title_full First‐in‐human trial to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of STR‐324, a dual enkephalinase inhibitor for pain management
title_fullStr First‐in‐human trial to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of STR‐324, a dual enkephalinase inhibitor for pain management
title_full_unstemmed First‐in‐human trial to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of STR‐324, a dual enkephalinase inhibitor for pain management
title_short First‐in‐human trial to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of STR‐324, a dual enkephalinase inhibitor for pain management
title_sort first‐in‐human trial to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of str‐324, a dual enkephalinase inhibitor for pain management
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292820/
https://www.ncbi.nlm.nih.gov/pubmed/34046921
http://dx.doi.org/10.1111/bcp.14931
work_keys_str_mv AT mosslaurencem firstinhumantrialtoassessthesafetytolerabilitypharmacokineticsandpharmacodynamicsofstr324adualenkephalinaseinhibitorforpainmanagement
AT berendscecilel firstinhumantrialtoassessthesafetytolerabilitypharmacokineticsandpharmacodynamicsofstr324adualenkephalinaseinhibitorforpainmanagement
AT vanbrummelenemiliemj firstinhumantrialtoassessthesafetytolerabilitypharmacokineticsandpharmacodynamicsofstr324adualenkephalinaseinhibitorforpainmanagement
AT kamerlingingridmc firstinhumantrialtoassessthesafetytolerabilitypharmacokineticsandpharmacodynamicsofstr324adualenkephalinaseinhibitorforpainmanagement
AT klaassenericas firstinhumantrialtoassessthesafetytolerabilitypharmacokineticsandpharmacodynamicsofstr324adualenkephalinaseinhibitorforpainmanagement
AT bergmannkirsten firstinhumantrialtoassessthesafetytolerabilitypharmacokineticsandpharmacodynamicsofstr324adualenkephalinaseinhibitorforpainmanagement
AT villevanessa firstinhumantrialtoassessthesafetytolerabilitypharmacokineticsandpharmacodynamicsofstr324adualenkephalinaseinhibitorforpainmanagement
AT juarezperezvictor firstinhumantrialtoassessthesafetytolerabilitypharmacokineticsandpharmacodynamicsofstr324adualenkephalinaseinhibitorforpainmanagement
AT benichouannieclaude firstinhumantrialtoassessthesafetytolerabilitypharmacokineticsandpharmacodynamicsofstr324adualenkephalinaseinhibitorforpainmanagement
AT groeneveldgeertjan firstinhumantrialtoassessthesafetytolerabilitypharmacokineticsandpharmacodynamicsofstr324adualenkephalinaseinhibitorforpainmanagement