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PHASE I STUDY OF VELIPARIB IN COMBINATION WITH GEMCITABINE
BACKGROUND: Veliparib (ABT-888) is an oral PARP inhibitor expected to increase gemcitabine activity. This phase I determined the maximal tolerable dose (MTD), dose-limiting toxicities (DLT), antitumor activity, pharmacokinetics (PK), and pharmacodynamics (PD) of veliparib combined with gemcitabine....
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| Izdano u: | Cancer Chemother Pharmacol |
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| Glavni autori: | , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2017
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5734661/ https://ncbi.nlm.nih.gov/pubmed/28770300 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00280-017-3409-3 |
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