Effect of Pasireotide Long Acting Release (LAR) on Gonadotroph Adenomas (LAR)
Primary Purpose
Gonadotroph Adenomas
Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
pasireotide LAR
Sponsored by
About this trial
This is an interventional treatment trial for Gonadotroph Adenomas focused on measuring pituitary tumor, endocrine
Eligibility Criteria
Inclusion Criteria:
- gonadotroph adenoma
Exclusion Criteria:
- visual impairment attributable to the adenoma
- radiation therapy
- active gallbladder disease
- uncontrolled diabetes
Sites / Locations
- University of Pennsylvania
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Pasireotide LAR
Arm Description
80 mg IM once monthly
Outcomes
Primary Outcome Measures
Number of Participants With Change in Size of the Adenoma by ≥3 mm in at Least Two Dimensions as Determined by MRI
MRI of the pituitary will be performed at baseline, Month 6 and Month 12 to demonstrate a decrease of ≥3 mm in at least two of three dimensions on MRI (cephalocaudal, transverse, and posterior-anterior). The outcome measure is defined as the number of participants who demonstrated a ≥3 mm decrease in adenoma size in two dimensions.
Secondary Outcome Measures
Number of Participants With Change in Serum FSH Concentration (mIU/mL) in Patients Who Have Gonadotroph Adenomas Treated With Pasireotide.
Serum FSH (mIU/mL) will be measured at baseline and then monthly for the 12 months of the study to determine if serum FSH concentrations decrease by 20%.
Full Information
NCT ID
NCT00929669
First Posted
June 23, 2009
Last Updated
October 20, 2017
Sponsor
University of Pennsylvania
1. Study Identification
Unique Protocol Identification Number
NCT00929669
Brief Title
Effect of Pasireotide Long Acting Release (LAR) on Gonadotroph Adenomas
Acronym
LAR
Official Title
Effect of Pasireotide LAR on Gonadotroph Adenomas: A Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2017
Overall Recruitment Status
Terminated
Why Stopped
unable to identify a third subject
Study Start Date
June 2009 (undefined)
Primary Completion Date
November 2011 (Actual)
Study Completion Date
November 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Pennsylvania
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine if administration of pasireotide LAR for one year to three patients with gonadotroph adenomas and elevated serum FSH concentrations will reduce the serum follicle-stimulating hormone (FSH) to normal and reduce the adenoma size.
Detailed Description
Gonadotroph adenomas are the most common pituitary macroadenomas. Currently no medical treatment as been found that decreases the size of these adenomas, so surgery is the only treatment. The reason to think that pasireotide might affect gonadotroph adenomas is that pasireotide binds avidly to somatostatin subtype 5 receptors, and gonadotroph adenomas express these receptors. For this study, three subjects who have gonadotroph adenomas, as judged by a macroadenoma of the pituitary and elevated serum FSH concentration, will be treated with a long-acting form of pasireotide once a month for one year. The effect of pasireotide on the size of the adenoma will be determined by MRI, and FSH secretion will be judged by the serum concentration.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gonadotroph Adenomas
Keywords
pituitary tumor, endocrine
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
2 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Pasireotide LAR
Arm Type
Experimental
Arm Description
80 mg IM once monthly
Intervention Type
Drug
Intervention Name(s)
pasireotide LAR
Other Intervention Name(s)
SOM230
Intervention Description
pasireotide LAR 80 mg IM once a month
Primary Outcome Measure Information:
Title
Number of Participants With Change in Size of the Adenoma by ≥3 mm in at Least Two Dimensions as Determined by MRI
Description
MRI of the pituitary will be performed at baseline, Month 6 and Month 12 to demonstrate a decrease of ≥3 mm in at least two of three dimensions on MRI (cephalocaudal, transverse, and posterior-anterior). The outcome measure is defined as the number of participants who demonstrated a ≥3 mm decrease in adenoma size in two dimensions.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Number of Participants With Change in Serum FSH Concentration (mIU/mL) in Patients Who Have Gonadotroph Adenomas Treated With Pasireotide.
Description
Serum FSH (mIU/mL) will be measured at baseline and then monthly for the 12 months of the study to determine if serum FSH concentrations decrease by 20%.
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
gonadotroph adenoma
Exclusion Criteria:
visual impairment attributable to the adenoma
radiation therapy
active gallbladder disease
uncontrolled diabetes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter J. Snyder, MD
Organizational Affiliation
University of Pennsylvania
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Effect of Pasireotide Long Acting Release (LAR) on Gonadotroph Adenomas
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