Individual Patient Expanded Access-Glembatumumab Vedotin
Primary Purpose
Metastatic gpNMB Expressing Triple Negative Breast Cancer
Status
No longer available
Phase
Locations
Study Type
Expanded Access
Intervention
glembatumumab vedotin
Sponsored by
About this trial
This is an expanded access trial for Metastatic gpNMB Expressing Triple Negative Breast Cancer
Eligibility Criteria
Inclusion Criteria:
- The patient is 18 years of age or older.
- The patient has histologically confirmed, gpNMB expressing, metastatic triple-negative breast cancer
- Overexpression of gpNMB in at least one tumor sample as determined by a Sponsor approved laboratory using IHC methods
- The patient does not have abnormal organ function, active autoimmune disease, active infections or additional concurrent conditions that would compromise the patient's ability to safely receive glembatumumb vedotin.
- The patient is not eligible for or cannot access ongoing glembatumumab vedotin clinical trials
- The patient does not qualify for, or cannot access, other comparable or satisfactory alternative therapy for triple negative breast cancer.
- The patient is able to read and understand, and has signed a patient informed consent form, which outlines the nature of the proposed treatment and the anticipated benefits and risks of treatment with glembatumumab vedotin.
Exclusion Criteria:
- History of allergic reactions attributed to compounds of similar composition to glembatumumab vedotin, MMAE, dolastatin or auristatin.
- Pregnant or breast-feeding women, and women or men who are not willing to use effective contraception during the time from signing of informed consent through two months after the last dose of glembatumumab vedotin treatment.
- The patient was previously treated with glembatumumab vedotin or previously enrolled on the METRIC trial (regardless of which arm they were randomized to).
- Any underlying medical condition that, in the investigator's or Sponsor's opinion, will make the administration of Glembatumumab vedotin hazardous to the patient, or would obscure the interpretation of adverse events.
Sites / Locations
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03067935
Brief Title
Individual Patient Expanded Access-Glembatumumab Vedotin
Study Type
Expanded Access
2. Study Status
Record Verification Date
May 2018
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
Celldex Therapeutics
4. Oversight
5. Study Description
Brief Summary
Celldex endeavors to make investigational products available to patients with life-threatening diseases who have exhausted other treatment options and where there is a reasonable expectation of benefit over risk. Requests for expanded access to glembatumumab vedotin in patients with gpNMB expressing triple negative breast cancer will be considered.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic gpNMB Expressing Triple Negative Breast Cancer
7. Study Design
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
glembatumumab vedotin
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Eligibility Criteria
Inclusion Criteria:
The patient is 18 years of age or older.
The patient has histologically confirmed, gpNMB expressing, metastatic triple-negative breast cancer
Overexpression of gpNMB in at least one tumor sample as determined by a Sponsor approved laboratory using IHC methods
The patient does not have abnormal organ function, active autoimmune disease, active infections or additional concurrent conditions that would compromise the patient's ability to safely receive glembatumumb vedotin.
The patient is not eligible for or cannot access ongoing glembatumumab vedotin clinical trials
The patient does not qualify for, or cannot access, other comparable or satisfactory alternative therapy for triple negative breast cancer.
The patient is able to read and understand, and has signed a patient informed consent form, which outlines the nature of the proposed treatment and the anticipated benefits and risks of treatment with glembatumumab vedotin.
Exclusion Criteria:
History of allergic reactions attributed to compounds of similar composition to glembatumumab vedotin, MMAE, dolastatin or auristatin.
Pregnant or breast-feeding women, and women or men who are not willing to use effective contraception during the time from signing of informed consent through two months after the last dose of glembatumumab vedotin treatment.
The patient was previously treated with glembatumumab vedotin or previously enrolled on the METRIC trial (regardless of which arm they were randomized to).
Any underlying medical condition that, in the investigator's or Sponsor's opinion, will make the administration of Glembatumumab vedotin hazardous to the patient, or would obscure the interpretation of adverse events.
12. IPD Sharing Statement
Learn more about this trial
Individual Patient Expanded Access-Glembatumumab Vedotin
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