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[VIRTUAL] General pharmacodynamics algorithm-based clinical protocol design with two to three dose-data points for single-drug, and ten data points for two-drug-combination synergy quantification, using computer simulation for digitalized data analysis and conclusions (Virtual Meeting: All Session Times Are U.S. EDT) - Apr 13, 2020 - Abstract #AACRI2020AACR-I_155; This report reaffirm Example 2 with the same drug combos against MX-1 mammary carcinoma xenograft in nude mice, using only 10 data points, which showed similar synergy at ED75 to ED97, CI= 0.82-0.79 for MX-1, and CI= 0.98-0.64 for HCT-116. In conclusion, the MAL-PD/BD and its equations, algorithms and computer simulation provide a rigorous, cost-effective, automated, quantitative biomedical R and D and general drug evaluation guidance in clinical trial design and data analysis, that save resources, time and efforts.
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Journal: Chemical and biological properties of new sealant-use cement materials. (Pubmed Central) - Dec 20, 2019 In conclusion, the MAL-PD/BD and its equations, algorithms and computer simulation provide a rigorous, cost-effective, automated, quantitative biomedical R and D and general drug evaluation guidance in clinical trial design and data analysis, that save resources, time and efforts. Three of four newly developed GICs modified with calcium, phosphate and fluoride ions were found to be superior to other sealant materials.
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Trial completion: T900607 in Treating Patients With Unresectable Liver Cancer (clinicaltrials.gov) - Feb 22, 2014 P2, N=0, Completed, Three of four newly developed GICs modified with calcium, phosphate and fluoride ions were found to be superior to other sealant materials. Active, not recruiting --> Completed
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Enrollment change, Metastases: TTP607 in Refractory Solid Malignancies (clinicaltrials.gov) - Jul 26, 2012 P1, N=0, Withdrawn, Active, not recruiting --> Completed N=40 --> 0
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