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Pre-Approval Access Single Patient Request for Talquetamab in Relapsed or Refractory Multiple Myeloma

Primary Purpose

Relapsed or Refractory Multiple Myeloma

Status
No longer available
Phase
Locations
International
Study Type
Expanded Access
Intervention
Talquetamab
Sponsored by
Janssen Research & Development, LLC
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an expanded access trial for Relapsed or Refractory Multiple Myeloma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)

Sites / Locations

  • DUMMY
  • DUMMY
  • DUMMY
  • DUMMY

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
August 12, 2022
Last Updated
September 13, 2023
Sponsor
Janssen Research & Development, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT05503550
Brief Title
Pre-Approval Access Single Patient Request for Talquetamab in Relapsed or Refractory Multiple Myeloma
Official Title
Pre-Approval Access Single Patient Request Treatment for Talquetamab for Treating Physician Use in Relapsed or Refractory Multiple Myeloma
Study Type
Expanded Access

2. Study Status

Record Verification Date
September 2023
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
Janssen Research & Development, LLC

4. Oversight

5. Study Description

Brief Summary
The purpose of this pre-approval access program is to provide talquetamab for the treatment of participants with relapsed or refractory multiple myeloma.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Relapsed or Refractory Multiple Myeloma

7. Study Design

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Talquetamab
Other Intervention Name(s)
JNJ-64407564
Intervention Description
Talquetamab will be administered subcutaneously (SC).

10. Eligibility

Minimum Age & Unit of Time
18 Years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Janssen Research & Development, LLC Clinical Trial
Organizational Affiliation
Janssen Research & Development, LLC
Official's Role
Study Director
Facility Information:
Facility Name
DUMMY
City
Dummy
ZIP/Postal Code
99999
Country
Belgium
Facility Name
DUMMY
City
Dummy
ZIP/Postal Code
99999
Country
Iceland
Facility Name
DUMMY
City
Dummy
ZIP/Postal Code
99999
Country
Portugal
Facility Name
DUMMY
City
Dummy
ZIP/Postal Code
99999
Country
Slovenia

12. IPD Sharing Statement

Learn more about this trial

Pre-Approval Access Single Patient Request for Talquetamab in Relapsed or Refractory Multiple Myeloma

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