Last updated: 11/03/2018 19:10:48
This product has been transferred to Novartis. GSK Clinical Study Register is no longer maintained for this study.

Drug Use Investigation of VOTRIENT Tablets

GSK study ID
116461
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
No longer a GSK study
No longer a GSK study
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: Drug Use Investigation of VOTRIENT Tablets
Trial description: This post-marketing surveillance (PMS) is conducted to collect safety and efficacy data in patients with STS who are treated with pazopanib tablets.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:

Progression-free survival

Timeframe: 1 year

Occurrence of adverse drug reactions

Timeframe: 1 year

Secondary outcomes:
Not applicable
Interventions:
Drug: Pazopanib
Enrollment:
300
Observational study model:
Cohort
Primary completion date:
Not applicable
Time perspective:
Prospective
Clinical publications:
Not applicable
Medical condition
Sarcoma, Soft tissue
Product
pazopanib
Collaborators
Not applicable
Study date(s)
December 2012 to September 2016
Type
Observational
Phase
Not applicable

Participation criteria

Sex
Female & Male
Age
Not applicable
Accepts healthy volunteers
none
  • Patients with STS
  • Patients treated with pazopanib tablets
  • None

Trial location(s)

No location data available.

Study documents

Scientific result summary
Available language(s): English

If you wish to request for full study report, please contact - [email protected]

Results overview

Refer to study documents

Recruitment status
No longer a GSK study
Actual primary completion date
Not applicable
Actual study completion date
Not applicable

Plain language summaries

Not applicable. GSK’s transparency policy provides for Plain Language Summaries for Interventional studies.

Additional information about the trial

Not applicable
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