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. 2009 Apr 2;3:27–44. doi: 10.2174/1874205X00903010027

Table 4.

Difficulties for the Development of Drugs that Modify the Evolution of AD

  • Scarcity of AD markers in preclinical stage

  • Scarcity of markers of AD phenotypes

  • Difficulty to obtain molecules with selective action on diseased cells

  • Most drugs will have weak effects since they act only on a part of the etiopathogenic chain

  • It is necessary to distinguish between symptomatic action and changes in the course of the disease

  • Need of a prolonged period of observation to prove delay in progression

  • Need to work with very wide human samples to achieve clinical evidence and statistical signification

  • High economic cost of trials designed to ascertain modifications in AD evolution