Last updated: 11/07/2018 16:17:53
Phase I Study of GW572016 in Patients with Solid Tumors <Clinical Pharmacology Study>
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: Phase I Study of GW572016 in Patients with Solid Tumors <Clinical Pharmacology Study>
Trial description: Phase I Study of GW572016 in Patients with Solid Tumors <Clinical Pharmacology Study>
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Nakagawa K, Minami H, Kanezaki M, Mukaiyama A, Minamide Y, Shimizu H, Sasaki Y, Fukuoka M.Phase I dose-escalation and pharmacokinetic trial of lapatinib (GW572016), a selective oral dual inhibitor of ErbB-1 and ErbB-2 tyrosine kinases, in Japanese patients with solid tumors.Japan Journal of Clinical Oncology.2009;39(2):116-123
Medical condition
Neoplasms, Colorectal
Product
lapatinib
Collaborators
Not applicable
Study date(s)
October 2002 to May 2004
Type
Not applicable
Phase
1
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2004-11-05
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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