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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.
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.
Afiliação
  • Moss LM; Centre for Human Drug Research, Leiden, the Netherlands.
  • Berends CL; Leiden University, Leiden, the Netherlands.
  • van Brummelen EMJ; Centre for Human Drug Research, Leiden, the Netherlands.
  • Kamerling IMC; Leiden University, Leiden, the Netherlands.
  • Klaassen ES; Centre for Human Drug Research, Leiden, the Netherlands.
  • Bergmann K; Centre for Human Drug Research, Leiden, the Netherlands.
  • Ville V; Leiden University, Leiden, the Netherlands.
  • Juarez-Perez V; Centre for Human Drug Research, Leiden, the Netherlands.
  • Benichou AC; Centre for Human Drug Research, Leiden, the Netherlands.
  • Groeneveld GJ; Stragen France, Lyon, France.
Br J Clin Pharmacol ; 88(1): 103-114, 2022 01.
Article em En | MEDLINE | ID: mdl-34046921
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 Cmax and AUCinf with an estimated t1/2 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).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neprilisina / Manejo da Dor Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans / Male Idioma: En Revista: Br J Clin Pharmacol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neprilisina / Manejo da Dor Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans / Male Idioma: En Revista: Br J Clin Pharmacol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Holanda