- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01797874
Pazopanib Maintenance for SCLC
December 5, 2019 updated by: Myung-Ju Ahn, Samsung Medical Center
Phase II Study of Pazopanib Maintenance for SCLC
To evaluate the efficacy of pazopanib maintenance after 1st line CTx for SCLC.
Study Overview
Study Type
Interventional
Enrollment (Actual)
97
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Seoul, Korea, Republic of, 135-710
- Samsung Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- histologically confirmed SCLC
- no disease progression after 4 cycles of etoposide/platinum 1st-line therapy
- history of 4 cycles of etoposide/platinum 1st-line therapy
- between 21 days and 42 days since C4D1 of etoposide/platinum
- no symptomatic brain meta
Exclusion Criteria:
- poor hepatic, renal function
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Pazopanib
pazopanib maintenance after 4 cycles of etoposide/platinum in SCLC
|
Experimental
Other Names:
|
Placebo Comparator: placebo
placebo after 4 cycles of etoposide/platinum chemotherapy in SCLC
|
placebo arm
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Progression-free survival
Time Frame: 12 months
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2013
Primary Completion (Actual)
February 1, 2017
Study Completion (Actual)
December 1, 2017
Study Registration Dates
First Submitted
February 21, 2013
First Submitted That Met QC Criteria
February 22, 2013
First Posted (Estimate)
February 25, 2013
Study Record Updates
Last Update Posted (Actual)
December 9, 2019
Last Update Submitted That Met QC Criteria
December 5, 2019
Last Verified
December 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2012-09-060-002
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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