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OncoMatch/Clinical Trials/NCT05972135

Outpatient Administration of Teclistamab or Talquetamab for Multiple Myeloma

Is NCT05972135 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Teclistamab and Talquetamab for multiple myeloma.

Phase 2RecruitingSCRI Development Innovations, LLCNCT05972135Data as of May 2026

Treatment: Teclistamab · Talquetamab · Tocilizumab · Oral DexamethasoneThis is a phase II study to evaluate the outpatient administration of Teclistamab or Talquetamab in Multiple Myeloma patients

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Extracted eligibility criteria

Cancer type

Multiple Myeloma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Must have received: proteasome inhibitor

has received 2 or more prior MM therapies including a PI, IMiD and CD38 antibody.

Must have received: immunomodulatory agent

has received 2 or more prior MM therapies including a PI, IMiD and CD38 antibody.

Must have received: CD38 antibody

has received 2 or more prior MM therapies including a PI, IMiD and CD38 antibody.

Cannot have received: gene modified adoptive cell therapy (CAR-T cells, NK cells, BCMA therapy)

For teclistamab arms only: Prior Gene modified adoptive cell therapy (eg, chimeric antigen receptor modified [CAR]-T cells, NK cells, or BCMA therapy)

Cannot have received: GPRC5D-targeting therapy

For talquetamab arm only: any prior GPRC5D-targeting therapy

Cannot have received: CAR-T cell therapy

For talquetamab arm only: Prior Grade 3 or higher CRS related to any T-cell redirection (e.g., CD-3 redirection technology or CAR-T cell therapy)

Cannot have received: BCMA bispecific antibody

For talquetamab arm only: Prior CAR-T or BCMA bispecific antibody therapy are allowed with the appropriate wash-out period: 1) Gene modified adoptive cell therapy (eg, chimeric antigen receptor modified [CAR]-T cells, NK cells) within 3 months, or 2) BCMA therapies (antibody-drug conjugates and bispecific antibodies, etc) within 21 days or at least 5 half-lives, whichever is less.

Lab requirements

Blood counts

Grade ≥3 hematologic AEs [excluded]

Kidney function

eGFR <20 ml/min or is dependent on dialysis [excluded]

Liver function

Adequate organ system function

Cardiac function

Presence of the following cardiac conditions: NYHA stage III or IV CHF, MI or CABG ≤6 months prior, history of clinically significant ventricular arrhythmia or unexplained syncope, severe non-ischemic cardiomyopathy, poorly controlled CAD and/or CHF, uncontrolled cardiac arrhythmia or clinically significant ECG abnormalities

Adequate organ system function. Has Grade ≥3 hematologic AEs or Grade ≥3, clinically significant non-hematologic AEs. eGFR <20 ml/min or is dependent on dialysis [excluded]. Presence of the following cardiac conditions: New York Heart Association stage III or IV congestive heart failure. Myocardial infarction or CABG ≤6 months prior to enrollment. History of clinically significant ventricular arrhythmia or unexplained syncope, not believed to be vasovagal in nature or due to dehydration. History of severe non-ischemic cardiomyopathy. Poorly controlled coronary artery disease and/or congestive heart failure. Uncontrolled cardiac arrhythmia or clinically significant ECG abnormalities.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Arizona Oncology Associates · Tucson, Arizona
  • Colorado Blood Cancer Institute · Denver, Colorado
  • Rocky Mountain Cancer Center · Denver, Colorado
  • Medical Oncology Hematology Consultants · Newark, Delaware
  • Florida Cancer Specialists · Lake Mary, Florida

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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