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A study with a partial subtype selective GABAA α2,3 agonist, using quantitative pharmacodynamic measurements in healthy subjects Poster copy Chen, X1,2 , Jaeger, J 3*, Lappalainen, J 4, Maruff, P 3, Smith, MA 5*, Cross, AJ4, van Gerven, JMA2 1Clinical Pharmacology Research Center, Peking Union Medical College Hospital, Beijing, China; 2Centre for Human Drug Research ,Leiden, The Netherlands; 3Cogstate, Melbourne Australia and New Haven CT, USA;4AstraZeneca, R&D, Wilmington Delaware and Cambridge MA; 5Shire Pharmaceuticals, PA, USA AIM To investigate the effects of AZD7325 on cognitive, visuomotor, neurophysiological and postural stability measures relative to lorazepam at doses that result in comparable or higher occupancy. ■ The slopes of the regression lines were flatter for AZD7325, particularly for the ΔLog(Sway)-ΔSPV relation and the ΔVASalertness-ΔSPV relation, compared to lorazepam (Figure 2). 2.86 ■ Design: single-dose, randomized, double-blind, 4-way crossover study in 16 healthy men ■ Treatments: AZD7325 10mg, AZD7325 2 mg, Lorazepam 2 mg, Placebo Identification 2.82 2.80 2.78 2.76 2.74 2.72 2.70 2.68 2.66 2.64 -2 -1 0 1 2 3 4 5 6 7 8 9 Detection, Identification, Chase test Visual and Verbal Learning International Shopping List (ISL), One Card Learning Long term memory ISL delayed recall Executive function Groton Maze group mean (SE) prop correct (arcsine) hours CogState test 1.00 0.95 0.90 0.85 0.80 0.75 0.70 0.65 0.60 0.55 0.50 0.45 0.40 -3 ΔSPV 90.00 low high loraz placebo Visual Learning -2 -1 0 1 2 3 4 hours 5 6 7 8 9 low high loraz placebo 80.00 70.00 60.00 40.00 30.00 20.00 Executive Functioning 10.00 0.00 -3 -2 -1 0 1 2 3 hours 4 5 6 7 8 ■ ■ ■ scales, 9 ΔSPV Figure 2.:ΔSPV-ΔVASalertness and ΔSPV-Δlog(Sway) relation ■ 50.00 CONCLUSIONS ■ The characteristic ΔSPV-relative effect profiles of AZD7325 vs. lorazepam suggests anxio-selectivity related to α2,3-selective GABAA agonism. However, exploration of higher doses may be warranted. ■ The lack of effects on most CNS-PD parameters ■ CNS-PD test battery: ■ Neurophysiological function: saccadic peak velocity (SPV), smooth pursuit Postural balance: Body sway Eye-hand coordination: Adaptive tracking Subjective effect: Visual analogue VASalertness AZD7325 10 mg low high loraz placebo 2.84 -3 ■CogState battery: Attention, processing speed, visuo-motor coordination Neither dose of AZD7325 affected VASalertness, SPV, sway, smooth pursuit, tracking, or any cognitive measures (Figure 1), which were all robustly impaired by lorazepam 2mg (all p<0.05). ■ METHODS Cognitive function AZD7325 2 mg group mean (SE) Errors) ■ ■ RESULTS ΔVAS alertness Does AZD7325, a novel α2,3-subtype selective GABAA modulator produce a benzodiazepine-like profile on cognition and neurophysiologic biomarkers at doses that result in high GABAA receptor occupancy? ■ Δlog(Sway) INTRODUCTION group mean (SE) speed (log10RT) ■ suggests lower cognitive and neurophysiological side-effect burden than non-selective benzodiazepines. Figure 1:Group mean (+SE) performance on CogState measures at each of the time points. Note: Detection and Chase test profiles were very similar to that observed on Identification task, shown above. The authors report no conflicts of interest for this work Centre for Human Drug Research | Zernikedreef 8 | 2333 CL Leiden | The Netherlands | Tel +31 71 52 46 400 | [email protected] | www.chdr.nl