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Journal: Evaluation of human adipose-derived stromal cell behaviour following exposure to Tamoxifen. (Pubmed Central) - Aug 12, 2022 Trial completion date: Oct 2021 --> Apr 2023 | Trial primary completion date: Oct 2021 --> Apr 2023 At physiologically relevant doses, Tamoxifen treatment did not result in any deleterious effect on ASC survival and functionality and is unlikely to negatively impact ASC based breast reconstruction strategies for breast cancer patients receiving this adjuvant hormonal therapy.
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Enrollment closed, Trial completion date: Afimoxifene in Reducing the Risk of Breast Cancer in Women With Mammographically Dense Breast (clinicaltrials.gov) - Sep 13, 2021 P2, N=152, Active, not recruiting, At physiologically relevant doses, Tamoxifen treatment did not result in any deleterious effect on ASC survival and functionality and is unlikely to negatively impact ASC based breast reconstruction strategies for breast cancer patients receiving this adjuvant hormonal therapy. Recruiting --> Active, not recruiting | Trial completion date: Sep 2022 --> Oct 2021
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Journal: Synthesis of Tamoxifen-Artemisinin and Estrogen-Artemisinin Hybrids Highly Potent Against Breast and Prostate Cancer. (Pubmed Central) - Jun 16, 2021 The most potent compounds were the estrogen-artemisinin hybrids 27 and 28 (EC 50 (PC-3) = 1.18 µM and 1.07 µM, correspondingly) against prostate cancer and hybrid 23 (EC 50 (MCF-7) = 2.08 µM) against breast cancer. These findings demonstrate the high potential of hybridization of artemisinin and estrogens to further improve their anticancer activities and to produce synergistic effects between linked pharmacophores.
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Trial completion date, Trial primary completion date: Afimoxifene in Reducing the Risk of Breast Cancer in Women With Mammographically Dense Breast (clinicaltrials.gov) - Mar 4, 2021 P2, N=152, Recruiting, These findings demonstrate the high potential of hybridization of artemisinin and estrogens to further improve their anticancer activities and to produce synergistic effects between linked pharmacophores. Trial completion date: Sep 2020 --> Sep 2022 | Trial primary completion date: Sep 2020 --> Sep 2021
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Journal: Elucidating Binding Sites and Affinities of ERα Agonists and Antagonists to Human Alpha-Fetoprotein by In Silico Modeling and Point Mutagenesis. (Pubmed Central) - Nov 12, 2020 We performed in silico point substitutions of amino acid residues to confirm their roles in HAFP-ligand interactions and showed that Thr132, Leu138, His170, Phe172, Ser217, Gln221, His266, His316, Lys453, and Asp478 residues, along with two disulfide bonds (Cys224-Cys270 and Cys269-Cys277), have key roles in both HAFP-estrogen and HAFP-antiestrogen binding. Data obtained in our study contribute to understanding mechanisms underlying protein-ligand interactions and anticancer therapy strategies based on ERα-binding ligands.
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Low dose tamoxifen and other approaches to improve chemoprevention uptake (Stars at Night Ballroom 1&2 -3rd level) - Aug 19, 2019 - Abstract #SABCS2019SABCS_24; Initial findings indicate the feasibility of this approach in attaining active concentrations in the breast and modulation of Ki-67 (Lee et al Cancer Chemother Pharmacol. 2015).
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