Expanded Access to Everolimus, for an Individual Patient With Uterine Sarcoma (CTMS#18-0020)
Primary Purpose
Uterine Sarcoma
Status
Available
Phase
Locations
Study Type
Expanded Access
Intervention
Everolimus
Sponsored by
About this trial
This is an expanded access trial for Uterine Sarcoma
Eligibility Criteria
Sites / Locations
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT03493165
First Posted
April 2, 2018
Last Updated
August 25, 2022
Sponsor
The University of Texas Health Science Center at San Antonio
1. Study Identification
Unique Protocol Identification Number
NCT03493165
Brief Title
Expanded Access to Everolimus, for an Individual Patient With Uterine Sarcoma (CTMS#18-0020)
Official Title
Expanded Access to Everolimus, for an Individual Patient With Uterine Sarcoma (CTMS#18-0020)
Study Type
Expanded Access
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Available
Study Start Date
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Primary Completion Date
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Study Completion Date
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3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Texas Health Science Center at San Antonio
4. Oversight
5. Study Description
Brief Summary
Single patient treatment with everolimus.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Uterine Sarcoma
7. Study Design
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Everolimus
Other Intervention Name(s)
Zortress, Afinitor, and Afinitor Disperz
Intervention Description
mTOR inhibitor
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
John Sarantopoulos, MD
Phone
210-450-1785
Email
sarantopoulo@uthscsa.edu
12. IPD Sharing Statement
Learn more about this trial
Expanded Access to Everolimus, for an Individual Patient With Uterine Sarcoma (CTMS#18-0020)
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