Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Murray Ducharme"'
Publikováno v:
Journal of Pharmacy & Pharmaceutical Sciences, Vol 18, Iss 5 (2015)
Purpose: Clinical studies have suggested that proton pump inhibitors may decrease levothyroxine absorption and an in vitro study suggested that the effect of pH on dissolution may differ with formulation. To determine the impact of formulation on the
Externí odkaz:
https://doaj.org/article/8dd88cfd3a754744946607c674c6eae4
Autor:
Murray, Ducharme, Claudia, Scarsi, Elisa, Bettazzi, Giuseppe, Mautone, Yvette, Lewis, Francesco S, Celi
Publikováno v:
Thyroid. 32:897-904
Autor:
Kevin W Garey, Martin Kankam, Julie Mercier, Corinne Seng Yue, Murray Ducharme, Anne J Gonzales-Luna, M Jahangir Alam, Khurshida Begum, Michael Silverman
Publikováno v:
Open Forum Infectious Diseases
Background ACX-362E, a novel DNA polIIIC inhibitor, is a narrow-spectrum antibacterial selectively active against certain Gram-positive bacteria, including Clostridioides difficile (MIC90 = 4 µg/mL). The objectives of this phase I study was to asses
Autor:
Jennifer B. Dressman, Paul Fackler, Leon Shargel, Terry Hyslop, Saji Thomas, Henning Blume, Yu Chung Tsang, Murray Ducharme, Mei-Ling Chen, Lorelei Lutter, Dennis Bashaw, Lawrence X. Yu, Masood Bhatti, José A.G. Morais, Eric Ormsby, Vinod P. Shah, Raja Velagapudi, Daan J.A. Crommelin
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Regulatory approaches for evaluating therapeutic equivalence of multisource (or generic) drug products vary among different countries and/or regions. Harmonization of these approaches may decrease the number of in vivo bioequivalence studies and avoi
Autor:
Mitchell A, Garrison, Lisa A, Hammond, Charles E, Geyer, Garry, Schwartz, Anthony W, Tolcher, Leslie, Smetzer, Jose A, Figueroa, Murray, Ducharme, John, Coyle, Chris H, Takimoto, Robert L, De Jager, Eric K, Rowinsky
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 9(7)
The purpose of this study was to assess the feasibility of administering exatecan, a water-soluble, potent camptothecin analogue, as a protracted 21-day continuous i.v. infusion (CIVI). The study also sought to determine the maximum tolerated dose (M