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NCT00169533

Rollover Study Of Lapatinib In Cancer Patients

Completed Phase 1 Last updated 17 November 2017
What this trial tests

Phase 1 trial testing GW572016 oral tablets in Neoplasms, Breast in 31 participants. Completed in 5 May 2009.

Timeline
19 August 2004
Primary endpoint
5 May 2009
5 May 2009

Quick facts

Lead sponsorGlaxoSmithKline
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment31
Start date19 August 2004
Primary completion5 May 2009
Estimated completion5 May 2009
Sites12 locations across Canada, United States, Israel

Drugs / interventions tested

Conditions studied

Sponsor

GlaxoSmithKline — full company profile →

Who can join

18 and older, any sex, with Neoplasms, Breast. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The EGF19060 study is a rollover study to evaluate the long term safety of lapatinib and to provide lapatinib to patients who had a positive response in previous lapatinib studies until lapatinib is available pending FDA approval.

Publications & conference data

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

Verify or expand the search:

Other trials of GW572016 oral tablets

Trials testing the same drug.

Other recruiting trials for Neoplasms, Breast

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/NCT00169533.

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