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NCT01253122

Comparative Bioavailability of TRx0037 and TRx0014 in Healthy Elderly Volunteers

Completed Phase 1 Last updated 2 December 2010
What this trial tests

Phase 1 trial testing TRx0037 in Alzheimer's Disease in 24 participants. Completed in 1 April 2010.

Timeline
1 February 2010
Primary endpoint
1 April 2010
1 April 2010

Quick facts

Lead sponsorTauRx Therapeutics Ltd
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposebasic science
Enrollment24
Start date1 February 2010
Primary completion1 April 2010
Estimated completion1 April 2010

Drugs / interventions tested

Conditions studied

Sponsor

TauRx Therapeutics Ltd — full company profile →

Who can join

55 and older, any sex, with Alzheimer's Disease. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

A randomised four way crossover design in which each subject will receive two dose levels of TRx-0037 and two doses of TRx-0014 over approximately a four week period in randomised order.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Alzheimer's Disease

Currently open trials in the same condition.

Other TauRx Therapeutics Ltd trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01253122.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing