Condition: Healthy Volunteers · Sponsor: RDC Clinical Pty Ltd
This randomized, double-blind, crossover trial (Phase IV) aims to compare the absorption of a novel permeability-enhanced oral vitamin B12 formulation (Ampli-B) versus standard oral vitamin B12 in 12 healthy adults aged 50 years and older. Each participant receives a single dose of each formulation in randomized sequence, separated by a minimum 10-day washout. The primary outcome is time to peak serum concentration (Tmax) of total and active vitamin B12 (holotranscobalamin). Secondary outcomes include Cmax and AUC parameters.
This description comes directly from the study's public registry record.
David Briskey · +61(0)731024486 · research@rdcglobal.com.au
Always discuss trial participation with your own doctor first.
| RDC Clinical | Brisbane, Queensland, Australia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07665671