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NCT06062537Active, not recruiting

Analysis of Effectiveness and Safety of Teclistamab in Relapsed and Refractory Multiple Myeloma Patients

Analysis of Effectiveness and Safety of Teclistamab in Relapsed and Refractory Multiple Myeloma Patients: a Collaborative Janssen - IFM Study IFM 2023-01: TEC-CARE

Source: ClinicalTrials.gov · Last updated 13 Apr 2026

Brief summary (registry, in English)

200 adult patients with multiple myeloma receiving teclistamb will be included. Effectiveness, safety, and condition of use of teclistamab in early access program (post-MA) will be assessed. Primary objective is the evaluation of overall response rate (ORR) of teclistamab according to IMWG criteria. This is a multicenter, prospective, observational study.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
200 (actual)
First submitted
22 Sept 2023
Start date
19 Sept 2023
Primary completion date
Dec 2026
Lead sponsor
Intergroupe Francophone du Myelome
NCT number
NCT06062537

What you commit to

  • Study type: Observational
  • Participants enrolled: 200
  • From 19 Sept 2023 to the primary completion date, Dec 2026
  • 31 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who received teclistamab as part of an interventional clinical trial

Other

  • Patients alive at the start of the study who did not receive study information or who objected to the collection of data
  • Patients who are initiating teclistamab as part of a current interventional clinical trial

Who the study is looking for

  • Adult patient (≥18 years) with multiple myeloma who will receive at least one dose of teclistamab (first dose of the step-up dose)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (31)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chu Amiens Picardie
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AmiensFranceUnknown status
CH d'ANNECY
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AnnecyFranceUnknown status
Centre hospitalier d'Argenteuil
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ArgenteuilFranceUnknown status
Hopital de la cote Basque
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BayonneFranceUnknown status
CHU de Besançon
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BesançonFranceUnknown status
CHU Bordeaux
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BordeauxFranceUnknown status
Centre hospitalier de Brive-la-Gaillarde
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Brive-la-GaillardeFranceUnknown status
CHU Caen
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CaenFranceUnknown status
Centre Hospitalier Métropole de Savoie
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ChambéryFranceUnknown status
CHU Clermont-Ferrand Site Estaing
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Clermont-FerrandFranceUnknown status
CHU Henri Mondor
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CréteilFranceUnknown status
CHU Dijon
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DijonFranceUnknown status
CH Dunkerque
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DunkirkFranceUnknown status
CHU de Lille
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LilleFranceUnknown status
Groupe Hospitalier Bretagne Sud
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LorientFranceUnknown status
Institut Paoli-Calmette
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MarseilleFranceUnknown status
CH de METZ
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MetzFranceUnknown status
CHU Saint-Eloi - CHU de Montpellier
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MontpellierFranceUnknown status
CHU de Nantes
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NantesFranceUnknown status
CHU de Nice
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NiceFranceUnknown status
Hopital Saint Louis
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ParisFranceUnknown status
Hôpital Necker
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ParisFranceUnknown status
Ch Perpignan
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PerpignanFranceUnknown status
Hôpital NOVO
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PontoiseFranceUnknown status
CHU de Rennes
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RennesFranceUnknown status
Centre Henri Becquerel
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RouenFranceUnknown status
Institut de Cancérologie Lucien Neuwirth, CHU Saint-Etienne
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Saint-Priest-en-JarezFranceUnknown status
Hôpital de Hautepierre
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StrasbourgFranceUnknown status
CHU Toulouse
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ToulouseFranceUnknown status
CHU de Tours
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ToursFranceUnknown status
CH Bretagne Atlantique
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VannesFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.