Last updated: 02/18/2024 17:40:28

Efficacy/effectiveness of pazopanib and trabectedin treatment for metastatic synovial sarcoma

GSK study ID
213368
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: Efficacy/effectiveness of pazopanib and trabectedin treatment for metastatic synovial sarcoma: systematic review and meta-analysis
Trial description: The objective of the study is to evaluate the efficacy/effectiveness of pazopanib and trabectedin for >=2nd line metastatic synovial sarcoma using data from regulatory documents, clinical trials, and observational studies with regards to overall response rate and other listed outcomes.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:

Overall response rate (ORR)

Timeframe: Up to 17 years

Secondary outcomes:

Overall Survival (OS)

Timeframe: Up to 17 years

Progression free survival (PFS)

Timeframe: Up to 17 years

Number of participants with partial response (PR)

Timeframe: Up to 17 years

Number of participants with stable disease (SD)

Timeframe: Up to 17 years

Interventions:
Not applicable
Enrollment:
0
Primary completion date:
2020-06-04
Observational study model:
Other
Time perspective:
Retrospective
Clinical publications:
Not applicable
Medical condition
Sarcoma, Synovial
Product
GSK3377794
Collaborators
NA
Study date(s)
November 2019 to April 2020
Type
Observational
Phase
Not applicable

Participation criteria

Sex
Female & Male
Age
18+ years
Accepts healthy volunteers
No
  • Adults with metastatic SS.
  • Studies among participants with STS, but reporting results for the SS subgroup, are in scope.
  • Studies among STS participants will be excluded if they do not report results for the SS subgroup separately.
  • Cross-sectional studies, and case reports will be excluded.

Trial location(s)

This study does not involve prospective enrollment of participants.

Study documents

Protocol
Available language(s): English
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
Study complete
Actual primary completion date
2020-06-04
Actual study completion date
2020-06-04

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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