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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01099540
Other study ID # 2009-09-090
Secondary ID
Status Completed
Phase Phase 2
First received April 6, 2010
Last updated December 28, 2015
Start date April 2010
Est. completion date March 2013

Study information

Verified date December 2015
Source Samsung Medical Center
Contact n/a
Is FDA regulated No
Health authority Korea: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

To determine the response rate of pazopanib when administered as monotherapy in patients with unresectable neuroendocrine tumor.


Recruitment information / eligibility

Status Completed
Enrollment 37
Est. completion date March 2013
Est. primary completion date March 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- low to intermediate grade neuroendocrine tumor not amenable to surgery or local therapy

Exclusion Criteria:

- poorly differentiated (high grade or anaplastic)/small cell, pheochromocytoma

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
Pazopanib
Pazopanib 800 mg qd daily

Locations

Country Name City State
Korea, Republic of Samsung Cancer Center Seoul

Sponsors (1)

Lead Sponsor Collaborator
Samsung Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary response rate 1~2 year Yes
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