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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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 |
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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 |
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