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NCT03126617 Clinical Trial

Expanded Access to Elotuzumab (Empliciti) for Multiple Myeloma

Multiple Myeloma Clinical Trial

Official title:
Expanded Access to Elotuzumab (Empliciti) for Multiple Myeloma

Clinical Trial Details — Status: No longer available

Administrative data
NCT number NCT03126617
Other study ID # EAP-01-CA204
Secondary ID
Status No longer available
Phase
First received
Last updated

Study information
Verified date November 2021
Source Bristol-Myers Squibb
Contact n/a
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial 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.

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.

Recruitment information / eligibility
Status No longer available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design

Related Conditions & MeSH terms

Intervention

Biological:
• Elotuzumab
Elotuzumab (Emplicitii) is a Signaling Lymphocytic Activation Molecule Family member 7 (SLAMF7) directed immunostimulatory antibody approved by the US Food and Drug Administration (FDA) and indicated in combination with lenalidomide and dexamethasone for the treatment of patients with multiple myeloma who have received one to three prior therapies. Please contact your physician for more details.

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Bristol-Myers Squibb
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