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Co-crystal of tramadol-celecoxib: preclinical and clinical evaluation of a novel analgesic.
Gascon, Neus; Almansa, Carmen; Merlos, Manuel; Miguel Vela, José; Encina, Gregorio; Morte, Adelaida; Smith, Kevin; Plata-Salamán, Carlos.
Afiliación
  • Gascon N; a Research & Development Area , Esteve Pharmaceuticals, S.A , Barcelona , Spain.
  • Almansa C; a Research & Development Area , Esteve Pharmaceuticals, S.A , Barcelona , Spain.
  • Merlos M; a Research & Development Area , Esteve Pharmaceuticals, S.A , Barcelona , Spain.
  • Miguel Vela J; a Research & Development Area , Esteve Pharmaceuticals, S.A , Barcelona , Spain.
  • Encina G; a Research & Development Area , Esteve Pharmaceuticals, S.A , Barcelona , Spain.
  • Morte A; a Research & Development Area , Esteve Pharmaceuticals, S.A , Barcelona , Spain.
  • Smith K; b Department of Clinical Pharmacology , Mundipharma Research Ltd, Cambridge Science Park , Cambridge , UK.
  • Plata-Salamán C; a Research & Development Area , Esteve Pharmaceuticals, S.A , Barcelona , Spain.
Expert Opin Investig Drugs ; 28(5): 399-409, 2019 05.
Article en En | MEDLINE | ID: mdl-31023091
ABSTRACT

INTRODUCTION:

Pain management is a major unmet need due to the suboptimal efficacy and undesirable side effects of current analgesics. Multimodal therapies recruiting complementary mechanisms of action may help address this. Co-crystals incorporating two active pharmaceutical ingredients (APIs) constitute an innovative approach to multimodal therapy, particularly if modification of the physicochemical properties of constituent APIs can be translated into clinical benefits. AREAS COVERED The preclinical and clinical profiles of Co-Crystal of Tramadol-Celecoxib (CTC), a novel API-API co-crystal (11 molecular ratio of rac-tramadol.hydrochloride and celecoxib) are described. EXPERT OPINION CTC may provide a relevant addition to pain therapy due to its i) unique co-crystal structure conferring differentiated intrinsic dissolution profiles on constituent APIs, ii) modified clinical pharmacokinetics (slower absorption of tramadol and faster absorption of celecoxib) compared with commercially available single-entity reference products (in agreement with modified dissolution rates), iii) superior benefit-risk ratio compared with reference products (suggested by preclinical synergistic antinociceptive effects, without potentiation of adverse effects), and iv) efficacy in a phase 2 trial of moderate to severe pain following extraction of ≥2 impacted third molars requiring bone removal, where CTC doses containing low doses of APIs exerted a significant effect. Phase 3 studies are currently ongoing.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dolor / Tramadol / Celecoxib Límite: Animals / Humans Idioma: En Revista: Expert Opin Investig Drugs Asunto de la revista: TERAPIA POR MEDICAMENTOS Año: 2019 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dolor / Tramadol / Celecoxib Límite: Animals / Humans Idioma: En Revista: Expert Opin Investig Drugs Asunto de la revista: TERAPIA POR MEDICAMENTOS Año: 2019 Tipo del documento: Article País de afiliación: España