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xyy0307
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2025-01-08 加入
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An FDA oncology analysis of CD3 bispecific constructs and first-in-human dose selection
1小时前
已完结
Relationships between preclinical cardiac electrophysiology, clinical QT interval prolongation and torsade de pointes for a broad range of drugs: evidence for a provisional safety margin in drug development
1个月前
已完结
Scientific white paper on concentration-QTc modeling
2个月前
已完结
The pharmacokinetics, pharmacodynamics and safety of oral doses of ilaprazole 10, 20 and 40 mg and esomeprazole 40 mg in healthy subjects: a randomised, open‐label crossover study
5个月前
已完结
Pharmacokinetics and Bioequivalence of Amlodipine Besylate Tablet in Healthy Chinese Volunteers Under Fasting and Fed Conditions
6个月前
已完结
Pharmacokinetics, Bioequivalence, and Safety Studies of Amlodipine Besylate in Healthy Subjects
6个月前
已完结
A Study to Compare Bioequivalence Approach Between FDA and EMA in a Highly Variable Drug: Pinaverium Bromide Film Tablets
7个月前
已完结
[Study of the bioequivalence of a new isosorbide dinitrate tablet formulation compared with the standard preparation]
7个月前
已关闭
Pharmacokinetics and Bioequivalence of Fixed‐Dose Combination of Simvastatin and Ezetimibe Tablets: A Randomized, Crossover, Open‐Label Study in Healthy Volunteers
8个月前
已完结
Pharmacokinetics and Safety of Ezetimibe/Simvastatin Combination Tablet
8个月前
已完结
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