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Absolute Bioavailability of Vemurafenib in Patients With BRAF(V600) Mutation-Positive Malignancies.
Zhang W, Colburn D, Simmons B, Papai Z, Bertran E, Schadt S, Husser C, Forbes H, Roethlisberger D, Hartung T. Zhang W, et al. Clin Pharmacol Drug Dev. 2020 May;9(4):496-504. doi: 10.1002/cpdd.773. Epub 2020 Feb 21. Clin Pharmacol Drug Dev. 2020. PMID: 32083398 Clinical Trial.
Patients received oral vemurafenib 960 mg twice daily on days 1 through 28, with a single intravenous infusion of (14) C-labeled vemurafenib solution (3 mL, corresponding to a radioactive dose of 18.5 kBq and a vemurafenib dose of 20 g) g …
Patients received oral vemurafenib 960 mg twice daily on days 1 through 28, with a single intravenous infusion of (14) C
A single-dose mass balance and metabolite-profiling study of vemurafenib in patients with metastatic melanoma.
Goldinger SM, Rinderknecht J, Dummer R, Kuhn FP, Yang KH, Lee L, Ayala RC, Racha J, Geng W, Moore D, Liu M, Joe AK, Bazan SP, Grippo JF. Goldinger SM, et al. Pharmacol Res Perspect. 2015 Mar;3(2):e00113. doi: 10.1002/prp2.113. Pharmacol Res Perspect. 2015. PMID: 25729580 Free PMC article.
This study characterized mass balance, metabolism, rates/routes of elimination, and disposition of (14)C-labeled vemurafenib in patients with metastatic melanoma. Seven patients with metastatic BRAF-mutated melanoma received unlabeled vemurafenib
This study characterized mass balance, metabolism, rates/routes of elimination, and disposition of (14)C-labeled vem