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NCT01004809: AVODART®PMS

AVODART® Alopecia Post-marketing Surveillance (PMS)

Completed Last updated 19 June 2018
What this trial tests

trial testing Dutasteride in Alopecia in 712 participants. Completed in 21 December 2012.

Timeline
29 April 2010
Primary endpoint
1 December 2012
21 December 2012

Quick facts

Lead sponsorGlaxoSmithKline
StatusCompleted
Study typeOBSERVATIONAL
Enrollment712
Start date29 April 2010
Primary completion1 December 2012
Estimated completion21 December 2012
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

GlaxoSmithKline — full company profile →

Who can join

Adults 18 to 41, male only, with Alopecia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Post-marketing surveillance(PMS) to monitor the safety and effectiveness of dutasteride in Korean androgenetic alopecia patients

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Safety and Tolerability of the Dual 5-Alpha Reductase Inhibitor Dutasteride in the Treatment of Androgenetic Alopecia.
    Choi GS, Kim JH, Oh SY, Park JM, et al · · 2016 · cited 21× · PMID 27489426 · DOI 10.5021/ad.2016.28.4.444

Verify or expand the search:

Other trials of Dutasteride

Trials testing the same drug.

Other recruiting trials for Alopecia

Currently open trials in the same condition.

Other GlaxoSmithKline 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/NCT01004809.

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