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Phase I trial evaluating the antiviral agent Cidofovir in combination with chemoradiation in cervical cancer patients
PURPOSE: This phase I trial aimed to assess the safety and determine the recommended Phase II dose (RP2D) of Cidofovir combined with chemoradiotherapy in patients with stage IB2-IVA cervical cancer. EXPERIMENTAL DESIGN: Incremental doses (1, 2.5, 5 and 6.5 mg/kg) of IV Cidofovir were administered we...
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| Publié dans: | Oncotarget |
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| Auteurs principaux: | , , , , , , , , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Impact Journals LLC
2016
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5041925/ https://ncbi.nlm.nih.gov/pubmed/27016411 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.8224 |
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