Outpatient Administration of Teclistamab or Talquetamab for Multiple Myeloma
This is a phase II study to evaluate the outpatient administration of Teclistamab or Talquetamab in Multiple Myeloma patients
Trial Details
- NCT ID
- NCT05972135
- Phase
- PHASE2
- Sponsor
- SCRI Development Innovations, LLC
- Status
- RECRUITING
- Cancer Type
- Relapsed/Refractory Multiple Myeloma
- Interventions
- Teclistamab
- Talquetamab
- Tocilizumab
- Oral Dexamethasone
- Locations (sample)
- Tucson, Arizona, United States|32.22174,-110.92648
- Denver, Colorado, United States|39.73915,-104.9847
- Denver, Colorado, United States|39.73915,-104.9847
- Newark, Delaware, United States|39.68372,-75.74966
- Lake Mary, Florida, United States|28.75888,-81.31784
Key Eligibility Criteria
- Be ≥18 years of age (or the higher legal age in the jurisdiction in which the study is taking place) at the time of informed consent
- Has documented diagnosis of MM according to the IMWG diagnostic criteria (Rajkumar 2011).
- Teclistamab or Talquetamab + Tocilizumab: has received 2 or more prior MM therapies including a PI, IMiD and CD38 antibody.
- Teclistamab + Oral Dexamethasone: has received 1 or more prior MM therapies including a PI, IMiD and/or CD38 antibody.
For full eligibility, visit ClinicalTrials.gov.