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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
Celldex Therapeutics
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an expanded access trial for Metastatic gpNMB Expressing Triple Negative Breast Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All Sexes

Inclusion Criteria:

  1. The patient is 18 years of age or older.
  2. The patient has histologically confirmed, gpNMB expressing, metastatic triple-negative breast cancer
  3. Overexpression of gpNMB in at least one tumor sample as determined by a Sponsor approved laboratory using IHC methods
  4. 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.
  5. The patient is not eligible for or cannot access ongoing glembatumumab vedotin clinical trials
  6. The patient does not qualify for, or cannot access, other comparable or satisfactory alternative therapy for triple negative breast cancer.
  7. 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:

  1. History of allergic reactions attributed to compounds of similar composition to glembatumumab vedotin, MMAE, dolastatin or auristatin.
  2. 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.
  3. The patient was previously treated with glembatumumab vedotin or previously enrolled on the METRIC trial (regardless of which arm they were randomized to).
  4. 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

    First Posted
    February 23, 2017
    Last Updated
    May 17, 2018
    Sponsor
    Celldex Therapeutics
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    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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