Other cognitive domains such as language, constructional ability, attention/concentration and psychomotor speed. should, be assessed, as well. Thus, the NfG provides for the assessment of a significant number of different, cognitive domains, including domains not tested by the ADAS-COG, such as psychomotor speed and attention. This reflects the previous recommendations of Inhibitors,research,lifescience,medical the International Working Group on Dementia Drug Guidelines cited earlier.7 However, no specific guidance is given regarding which particular tests should be used in the cognitive assessment. Instead the authors state that: The Alzheimer’s Disease Assessment Scale (ADAS) cognitive subscale, dealing with memory,

language, construction and praxis, orientation, is widely used. However, this remains an open research field. This appears to underline the EWP’s willingness to consider tests other Inhibitors,research,lifescience,medical than the ADAS-COG. Vorinostat solubility dmso efficacy measurement for trials conducted

in the USA The ADAS-COG has become the “gold” standard for dementia drug trials in the USA, in spite of its acknowledged deficiencies.6 An Inhibitors,research,lifescience,medical attempt has been made to remedy the absence of tests of attention from the original version by the inclusion of two additional nonautomated tests, bringing the total number of subtests to 13. Given the status of the ADAS-COG and its continued apparent, popularity, the inclusion of this assessment in pivotal phase 3 trials of dementia drugs is highly recommended. It should also be included in larger phase 2 trials, though not necessarily as the primary outcome. Here, other more sensitive procedures or tests that cover major domains of function not covered by the ADAS-COG could be considered as primary outcomes, as the purpose of phase 2 trials Inhibitors,research,lifescience,medical is to identify optimal doses and dosing strategies, and also of course proof of concept. In spite of a perception that ADAS-COG is the only acceptable outcome measure for Inhibitors,research,lifescience,medical use in AD clinical drug trials, an influential guidance paper published

by Leber during his time with the FDA did not. mandate the use of the ADAS-COG.32 The requirement for coprimary efficacy Given that dementia is prima facie a disorder of cognition, it at. first seems entirely reasonable to consider granting marketing approval to drugs that, occasion cognitive improvement. However, an important consideration for regulators is the clinical relevance of the observed cognitive changes. Traditionally, a four-point ADAS-COG advantage of drug over much placebo has been seen as sufficient evidence of efficacy for regulators to issue marketing approval. However, recent, reviews of the efficacy of licensed drugs have cast considerable doubt on the validity of this assumption. For example, in their 2001 review of dementia drugs, the UK’s National Institute for Clinical Excellence39 stated that: It is not clear the extent to which cognitive measures such as ADAS-COG or MM.