Safety evaluation in healthy Colombian volunteers of P2Et extract obtained from caesalpinia spinosa: Design 3+3 phase I clinical trial
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Date
2022-02-23Authors
Duran, María I.Ballesteros-Ramírez, Ricardo
Téllez Arévalo, Angélica María
Torregrosa Almonacid, Lilian
Olejua Villa, Peter Alfonso
Galvis Navarrete, Silvia Helena
Urueña, Claudia Patricia
Fiorentino, Susana
Corporate Author(s)
Pontificia Universidad Javeriana. Facultad de Medicina. Departamento de Ciencias Fisiológicas
Pontificia Universidad Javeriana. Facultad de Medicina. Departamento de Cirugía y Especialidades. Cirugía General
Type
Artículo de revista
ISSN
1741-427X / 1741-4288 (Electrónico)
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Abstract
The polyphenol-enriched extract called P2Et derived from Caesalpinia spinosa (C. spinosa) had antitumor and immunomodulatory activities reported in breast cancer, leukemia, and melanoma. The aim of this study was to evaluate the safety and maximum tolerated dose of P2Et extract in Colombian healthy volunteers in a phase 1 clinical trial, open labelled, single-arm, dose-escalation design 3 + 3. Seven healthy volunteers were included; P2Et was administrated in capsules of 600 mg/d for 28 days. Analysis by intention to treat was performed. 4 volunteers showed adverse events and discontinued the intervention. 94.6% of AE were grade 1, and most of AE had a reasonable possibility of a relationship with the P2Et (83.8%). We found that the oral administration of P2Et is safe in healthy humans with a maximum tolerated dose of 600 mg/d. There was no severe toxicity; most of the adverse events were mild, without significant changes in the safety parameters evaluated.
Spatial coverage (cities)
Bogotá (Colombia)Spatial coverage
ColombiaLink to the resource
https://www.hindawi.com/journals/ecam/2022/7943001/Source
Evidence-Based Complementary and Alternative Medicine; Volumen 2022 , Páginas 1 - 11 (2022)
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