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A Phase I Study of Intravenous Fenretinide (4-HPR) for Patients with Malignant Solid Tumors
BACKGROUND: Fenretinide is a synthetic retinoid that can induce cytotoxicity by several mechanisms. Achieving effective systemic exposure with oral formulations has been challenging. An intravenous lipid emulsion fenretinide formulation was developed to overcome this barrier. We conducted a study to...
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| 出版年: | Cancer Chemother Pharmacol |
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| 主要な著者: | , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2021
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8058950/ https://ncbi.nlm.nih.gov/pubmed/33423090 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00280-020-04224-8 |
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