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Analysis of Effectiveness and Safety of Teclistamab in Relapsed and Refractory Multiple Myeloma Patients (TEC-CARE)

I

Intergroupe Francophone du Myelome

Status

Active, not recruiting

Conditions

Multiple Myeloma

Study type

Observational

Funder types

NETWORK
Industry

Identifiers

NCT06062537
IFM 2023-01

Details and patient eligibility

About

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.

Enrollment

200 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

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

Trial contacts and locations

31

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Central trial contact

Amandine Huguet; Chanaz Louni

Data sourced from clinicaltrials.gov

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