Expanded Access to Elotuzumab (Empliciti) for Multiple Myeloma

Sponsor
Bristol-Myers Squibb (Industry)
Overall Status
No longer available
CT.gov ID
NCT03126617
Collaborator
(none)

Study Details

Study Description

Brief Summary

At BMS, we work with physicians/investigators to make investigational products available to patients with life-threatening diseases that have exhausted other treatment options and where there is a reasonable expectation of benefit over risk.

When contacted by a treating physician, BMS will consider requests for providing early patient access to Elotuzumab in patients with multiple myeloma who are residents of Belgium, Thailand, Turkey, Argentina, and Colombia.

Condition or Disease Intervention/Treatment Phase
  • Biological: Elotuzumab

Detailed Description

Choosing to participate in an early patient access program is an important personal decision. Talk with your doctor and family members or friends about deciding to participate in an early patient access program.

To learn more about early patient access programs, your doctor may contact BMS using the information provided below.

Study Design

Study Type:
Expanded Access
Official Title:
Expanded Access to Elotuzumab (Empliciti) for Multiple Myeloma

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All

    Specific eligibility criteria must be met for access outside of a clinical trial.

    These inclusion criteria include:
    • The illness must be serious or life threatening

    • There are no other viable options (including approved products or active clinical trials)

    • There is sufficient evidence that the potential benefit to the patient would likely outweigh the potential risks based on what is known at the time

    • Other defined inclusion/exclusion criteria could be applicable.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Bristol-Myers Squibb

    Investigators

    • Study Director: Bristol-Myers Squibb, Bristol-Myers Squibb

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Bristol-Myers Squibb
    ClinicalTrials.gov Identifier:
    NCT03126617
    Other Study ID Numbers:
    • EAP-01-CA204
    First Posted:
    Apr 24, 2017
    Last Update Posted:
    Nov 29, 2021
    Last Verified:
    Nov 1, 2021
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 29, 2021