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Phase 2 Clinical Trial Case Study

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1. The Ethics of Consent Forms in Phase-II Clinical Trials. The main purpose of a consent form is to acknowledge a voluntarily patient’s rights in a clinical practice or research including the main purpose of the process, what kind and method of treatments, and most importantly, the benefit-risk analysis of it. In this particular aspect, the patient must be transparently explained of what will be the possible benefits and potential harm of it. In this case, it is scientifically acceptable that drugs with chemically similar structure don’t always have to have similar activity as the test had already proven it, where the similar drug cause side effects and was disapproved during the phase-I trial, and the new drug itself didn’t show those adverse …show more content…

By creating a ‘patent court’, it could replace ‘generalized judges’ to a more ‘specialized’ ones perfectly-suited in hearing patent cases because they also understand the technical aspects of it. This would lead to a more reliable, efficient and consistent decision-making. However, opponents of this notion may argued that this could bring disadvantages in the patent system where a higher possibility of bias could occur from unequally distributed knowledge and experience among judges and attorneys, and also from the narrowing-down of judge’s perspective that could prompt them to either under-estimate or (more possibly) over-estimate the necessity of acknowledging intellectual property rights. In response to these arguments, there can be a specialized education and training conducted for these judges and attorneys to make them more qualified for this type of court that could differentiate which kind of patent should be approved and which one doesn’t in a more objective way. These ‘specialized judges’ will base their decisions not only from the law point of view, but also from its technical aspect which will make the decision more reliable. The judges could also be provided with technical expert assistances that can give them neutral but more significant point of views. Opponents might …show more content…

In other words, it is like “sell whatever you want, but don’t get yourself caught”. These seems to be so irresponsible especially for profit-driven manufacturers. Furthermore, even though the FDA (in cooperation with the FTC) have already regulate product advertisement, there are still so many false advertising claiming that their product somehow could be used for diagnosis and curing certain diseases. In this matter, we could not give the consumer full responsibility to determine on their own which ones are safe as most of the people lack the related knowledge. In other examples, even though the advertising is ‘properly-written’ and acceptable under FTC regulations, they still provide us with some scientific facts that the products showed indication of diagnostic and curing effects, but even the source-reliability could still be questioned. Nevertheless, most people will still get fooled easily by these claims, especially from products sold online that also provide pictures of random celebrities as if they are consuming these products (in fact they are not!) and/or some un-reliable testimonial photos. Robert Longley from about.com reported that in 2014, the FDA have sent warning letters to 16 dietary supplement distributors that made false and

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