drugset / Trial / NCT01213355

Scopolamine Challenge Study

NCT01213355

Phase 1 Completed 38 enrolled Pfizer
RandomizedCrossoverDouble-blindOther

Summary

It is hypothesized that PF-05212377 (SAM-760) will reverse scopolamine induced cognitive impairments in healthy adults subjects.

Timeline

Start
2011-04
Primary completion
2011-08
Completion
2011-08

Drugs

EvaluationDrugModalityDoseRoute
Comparator Donepezil Small molecule 10 mg Oral
Subject PF-05212377 Small molecule 5 mg Oral
Subject PF-05212377 Small molecule 20 mg Oral
Subject PF-05212377 Small molecule 60 mg Oral
Background Scopolamine Unknown 0.5 mg Subcutaneous

Indications

No indication recorded.