Compassionate Use: Progressive Metastatic Castrate Resistant Prostate Cancer; Monotherapy Treatment With Trametinib
Primary Purpose
Progressive Metastatic Castrate Resistant Prostate Cancer
Status
No longer available
Phase
Locations
Study Type
Expanded Access
Intervention
Trametinib 2 mg
Sponsored by
About this trial
This is an expanded access trial for Progressive Metastatic Castrate Resistant Prostate Cancer
Eligibility Criteria
Inclusion Criteria:
- Progressive Metastatic Castrate Resistant Prostate Cancer
Exclusion Criteria:
- Absence of Progressive Metastatic Castrate Resistant Prostate Cancer
Sites / Locations
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT03386071
First Posted
December 21, 2017
Last Updated
January 14, 2019
Sponsor
Jonsson Comprehensive Cancer Center
Collaborators
Novartis
1. Study Identification
Unique Protocol Identification Number
NCT03386071
Brief Title
Compassionate Use: Progressive Metastatic Castrate Resistant Prostate Cancer; Monotherapy Treatment With Trametinib
Official Title
Individual Patient Program for Patient With Progressive Metastatic Castrate Resistant Prostate Cancer; Monotherapy Treatment With Trametinib
Study Type
Expanded Access
2. Study Status
Record Verification Date
January 2019
Overall Recruitment Status
No longer available
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Jonsson Comprehensive Cancer Center
Collaborators
Novartis
4. Oversight
5. Study Description
Brief Summary
The dosage of trametinib for oral administration is 2mg once daily. The patient is instructed to take the trametinib oncedaily dose at approximately the same time each day, by mouth with approximately 200 mL (almost 1 cup) of water on an empty stomach, either 1 hour before or 2 hours after a meal.
Detailed Description
The dosage of trametinib for oral administration is 2mg once daily. The patient is instructed to take the trametinib once daily dose at approximately the same time each day, by mouth with approximately 200 mL (almost 1 cup) of water on an empty stomach, either 1 hour before or 2 hours after a meal.
The patient will be provided with complete dosing instructions from his treating physician. If the subject is instructed that if he vomits after taking either of the medications provided under this program, he should not retake the dose. The patient should take the next dose as originally scheduled. If a dose is missed, the patient should not double the next regularly scheduled dose. However, the patient can take the missed dose immediately if the next scheduled dose is at least 12 hours later. If the next scheduled dose is due in less than 12 hours, the patient is instructed to skip the dose and resume dosing the next day at the regular time. Then to take the next dose at the usual time the subject is scheduled to take it. It is not known for how long the subject will remain in the program because each patient may respond differently to the treatment. The length of time the patient will take trametinib therapy will depend on his cancer status and how well he tolerates the drugs. If he experiences severe side effects, he is instructed to call his treating physician immediately. The treating physician may advise him stop compassionate used of trametinib or may advise him to lower the dose. Trametinib may also be stopped completely at his Treating Physician's discretion. The treating physician will use his/her clinical expertise considering the intensity of the adverse effect and/or the results of your laboratory tests to make his/her decision. The Treating Physician may consult with the Novartis Country Pharma Organization Medical Advisor/Director about dose interruptions or modifications.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Progressive Metastatic Castrate Resistant Prostate Cancer
7. Study Design
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Trametinib 2 mg
Intervention Description
The dosage of trametinib for oral administration is 2mg once daily.
10. Eligibility
Sex
Male
Gender Based
Yes
Gender Eligibility Description
Prostate
Minimum Age & Unit of Time
18 Years
Eligibility Criteria
Inclusion Criteria:
Progressive Metastatic Castrate Resistant Prostate Cancer
Exclusion Criteria:
Absence of Progressive Metastatic Castrate Resistant Prostate Cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthew Rettig, M.D.
Organizational Affiliation
Jonsson Comprehensieve Cancer Center
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Compassionate Use: Progressive Metastatic Castrate Resistant Prostate Cancer; Monotherapy Treatment With Trametinib
We'll reach out to this number within 24 hrs