Teclistamab Expanded Access Treatment Protocol for Relapsed or Refractory Multiple Myeloma Patients
Overview
The purpose of this expanded access treatment protocol is to provide patients access to teclistamab prior to market authorization. The program is limited to patients with relapsed or refractory multiple myeloma who have exhausted all treatment options available as local standard of care and who are not eligible for a teclistamab clinical trial.
Full Title of Study: “Teclistamab US Expanded Access Treatment Protocol for Patients With Relapsed or Refractory Multiple Myeloma”
Study Type
- Study Type: Expanded Access
Interventions
- Drug: Teclistamab
- Teclistamab will be administered subcutaneously (SC).
Participating in This Clinical Trial
Inclusion Criteria
- Patient diagnosed with Relapsed or Refractory Multiple Myeloma – Patient exhausted all commercially approved and clinically appropriate (not patient or physician preference) treatment options, and is ineligible for a clinical trial
Gender Eligibility: All
Minimum Age: 18 Years
Maximum Age: N/A
Investigator Details
- Lead Sponsor
- Janssen Research & Development, LLC
- Provider of Information About this Clinical Study
- Sponsor
- Overall Official(s)
- Janssen Research & Development, LLC Clinical Trial, Study Director, Janssen Research & Development, LLC
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