Trials / Completed
CompletedNCT00725764
Phase 2 Study of GSK1363089 (Formerly XL880) in Adults With Squamous Cell Cancer of the Head and Neck
A Phase 2 Study of the MET RTK Inhibitor GSK1363089 (Formerly XL880) in Subjects With Recurrent or Metastatic Squamous Cell Cancer of the Head and Neck
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 14 (actual)
- Sponsor
- GlaxoSmithKline · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study is being conducted to determine the best confirmed response rate, safety, and tolerability of GSK1363089 treatment in adult subjects with squamous cell carcinoma of the head and neck (SCCHN). GSK1363089 is a new chemical entity that inhibits multiple receptor tyrosine kinases (RTKs) with growth-promoting and angiogenic properties. The primary targets of GSK1363089 are the HGF and vascular endothelial growth factor (VEGF) RTK families (eg, MET, VEGFR2/kinase insert domain receptor \[KDR\]). Since MET overexpression has been associated with poorer prognosis and MET tyrosine kinase mutations have been reported in SCCHN, inhibition of MET receptor and VEGFR2/KDR activation by agents such as GSK1363089 may be of therapeutic benefit in this patient population.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | GSK1363089 (foretinib) | Multitargeted tyrosine kinase inhibitor |
Timeline
- Start date
- 2007-08-27
- Primary completion
- 2009-05-02
- Completion
- 2009-05-02
- First posted
- 2008-07-30
- Last updated
- 2017-10-16
- Results posted
- 2017-10-16
Locations
11 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00725764. Inclusion in this directory is not an endorsement.