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European Journal of Drug Metabolism and Pharmacokinetics|June 30, 2018
Pharmacokinetics of Tramadol and Celecoxib in Japanese and Caucasian Subjects Following Administration of Co-Crystal of Tramadol-Celecoxib (CTC): A Randomised, Open-Label StudyHelen Dooner, Gill Mundin, Sabine Mersmann, et al.Clinical Drug Investigation|July 16, 2018
The Effect of Food on Tramadol and Celecoxib Bioavailability Following Oral Administration of Co-Crystal of Tramadol-Celecoxib (CTC): A Randomised, Open-Label, Single-Dose, Crossover Study in Healthy VolunteersGregorio Encina, Mercedes Encabo, Marisol Escriche, et al.Clinical Therapeutics|June 25, 2021
Celecoxib-tramadol co-crystal: A Randomized 4-Way Crossover Comparative Bioavailability StudyJesús Cebrecos, James D Carlson, Gregorio Encina, et al.Drugs in R&D|May 2, 2013
Pharmacokinetic dose proportionality between two strengths (12.5 mg and 25 mg) of doxylamine hydrogen succinate film-coated tablets in fasting state: a single-dose, randomized, two-period crossover study in healthy volunteersSebastián Videla, Jesús Cebrecos, Mounia Lahjou, et al.British Journal of Clinical Pharmacology|September 10, 2017
Pharmacokinetics of multiple doses of co-crystal of tramadol-celecoxib: findings from a four-way randomized open-label phase I clinical trialSebastián Videla, Mounia Lahjou, Anna Vaqué, et al.British Journal of Clinical Pharmacology|August 16, 2017
Single-dose pharmacokinetics of co-crystal of tramadol-celecoxib: Results of a four-way randomized open-label phase I clinical trial in healthy subjectsSebastián Videla, Mounia Lahjou, Anna Vaqué, et al.Acta Pharmaceutica Sinica. B|February 23, 2023
Bispecific sigma-1 receptor antagonism and mu-opioid receptor partial agonism: WLB-73502, an analgesic with improved efficacy and safety profile compared to strong opioidsAlba Vidal-Torres, Begoña Fernández-Pastor, Mónica García, et al.Pageof 2