Analysis of the Resistance and Sensitivity Mechanisms to Teclistamab by Focusing on Single Immune Cell Examination
Condition(s) studied
Investigational drug(s) / intervention(s)
Bone marrow sampling: Bone marrow sampling collected at 12 weeks after initiation treatment (day 1 cycle 4)
Study summary
The aim of this study is to discover the immune and oncogenomic features that distinguish patients who respond to teclistamab from patients who are primarily resistant. Moreover, phenotypic and genotypic characteristics that occur with secondary resistance to teclistamab will be analyzed.
Eligibility
Primary outcome measure(s)
- Response to teclistamab at 12 weeks — at day 1 Cycle 4 (each cycle is 28 days)
response according to International Myeloma Working Group criteria
Trial sites (18)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU d'Amiens | Amiens | France | Recruiting |
| CHU de Caen | Caen | France | Recruiting |
| Polyclinique du Parc Drevon | Dijon | France | Recruiting |
| CH Annecy Genevois | Epagny Metz- Tessy | France | Recruiting |
| CHU de Lille | Lille | France | Recruiting |
| Centre Léon Bérard | Lyon | France | Recruiting |
| CHU de Montpellier | Montpellier | France | Recruiting |
| Hôpital Saint-Louis | Paris | France | Recruiting |
| Hôpital Saint-Antoine | Paris | France | Recruiting |
| Hôpital Necker | Paris | France | Recruiting |
| CHU de Bordeaux | Pessac | France | Recruiting |
| CHU de Lyon | Pierre-Bénite | France | Recruiting |
| CHU de Poitiers | Poitiers | France | Recruiting |
| CHU de Rennes | Rennes | France | Recruiting |
| CH Saint-Etienne | Saint-Priest-en-Jarez | France | Recruiting |
| CHU de Toulouse | Toulouse | France | Recruiting |
| CHU de Tours | Tours | France | Recruiting |
| CHRU Nancy | Vandœuvre-lès-Nancy | France | Recruiting |
More University Hospital, Toulouse trials in France
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05945524 on ClinicalTrials.gov ↗ ← All trials in France