Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
A Study of Talquetamab and Teclistamab Each in Combination With a Programmed Cell Death Receptor-1 (PD-1) Inhibitor for the Treatment of Participants With Relapsed or Refractory Multiple Myeloma
NCT05338775 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of the study is to identify the safe dose(s) of a PD-1 inhibitor in combination with talquetamab or teclistamab, and to characterize the safety and tolerability of talquetamab or teclistamab when administered in combination with a PD-1 inhibitor.
Conditions Studied
Interventions
- DRUG Teclistamab
- DRUG Talquetamab
- DRUG PD-1 Inhibitor
Study Locations (19)
Other
- CHU de Montpellier Hopital Saint Eloi — Montpellier
- CHU de Nantes hotel Dieu — Nantes
- CHU Poitiers - Hopital la Miletrie — Poitiers
- Institut Universitaire du Cancer Toulouse Oncopole — Toulouse
- Universitatsklinikum Carl Gustav Carus Dresden — Dresden
- Universitaetsklinikum Hamburg Eppendorf — Hamburg
- Universitaetsklinikum Heidelberg — Heidelberg
- Universitatsklinikum Wurzburg — Würzburg
- Hosp. Univ. Germans Trias I Pujol — Badalona
- Hosp Univ Fund Jimenez Diaz — Madrid
- Clinica Univ. de Navarra — Pamplona
- Hosp Clinico Univ de Salamanca — Salamanca
New York
- The Blavatnik Family Chelsea Medical Center at Mount Sinai — New York
- Icahn School of Medicine at Mount Sinai — New York
- Memorial Sloan Kettering Cancer Center — New York
Tennessee
- Sarah Cannon Research Institute — Nashville
- Vanderbilt Ingram Cancer Center — Nashville
Colorado
- Colorado Blood Cancer Institute — Denver
North Carolina
- Wake Forest Baptist Medical Center — Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 74 participants |
| Start Date | 2022-05-25 |
| Est. Completion | 2027-05-03 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05338775
The ClinicalTrials.gov registry entry for NCT05338775 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 74 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Janssen Research & Development, which has 442 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Relapsed/ Refractory Multiple Myeloma appearing as the primary indexed condition, and to 3 interventions — of which Teclistamab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05338775 reports 19 study locations spanning 5 distinct geographic areas — top geographies include Other, New York, Tennessee. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05338775 about?
NCT05338775 is a clinical study titled "A Study of Talquetamab and Teclistamab Each in Combination With a Programmed Cell Death Receptor-1 (PD-1) Inhibitor for the Treatment of Participants With Relapsed or Refractory Multiple Myeloma". The purpose of the study is to identify the safe dose(s) of a PD-1 inhibitor in combination with talquetamab or teclistamab, and to characterize the safety and tolerability of talquetamab or teclistamab when administered in combination with a PD-1 inhibitor.
What is the current status of trial NCT05338775?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 74 participants. The study started on 2022-05-25. Estimated completion is 2027-05-03.
What conditions does trial NCT05338775 study?
This clinical trial studies the following conditions: Relapsed/ Refractory Multiple Myeloma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05338775?
The interventions under investigation include: Teclistamab (DRUG), Talquetamab (DRUG), PD-1 Inhibitor (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05338775?
This trial is sponsored by Janssen Research & Development, which has 442 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05338775 being conducted?
This trial has 19 study locations across Colorado, New York, North Carolina, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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