Multiple Myeloma Clinical Trials

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EFfIcacy and Tolerability of FIXed Duration Teclistamab and Talquetamab FOR FRAIL Patients With Newly Diagnosed Multiple Myeloma (2 Cohort Study) - the EMN 37 FITFIX FOR FRAIL Trial

Status: Recruiting
Location: See all (29) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This is a multicenter, open-label phase II study with 2 parallel cohorts for frail patients with newly diagnosed multiple myeloma treated with daratumumab in combination with teclistamab and talquetamab. The main purpose of this study is to determine the progression free survival at 18 months in patients treated with teclistamab and daratumumab (Cohort 1) or talquetamab and daratumumab (Cohort 2).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient is ≥18 years of age and capable of giving informed consent and must sign an informed consent form (ICF), indicating that they understand the purpose of, and procedures required for, the study and is willing to participate in the study

• Newly diagnosed and treatment-naïve patients with a confirmed diagnosis of MM with measurable disease according to IMWG criteria

• Measurable disease defined as M-protein in the serum (≥1 g/dL) or serum free light chain assay ≥10 mg/dL \[≥100 mg/L\] and abnormal serum immunoglobulin kappa/lambda FLC ratio

• Frail according to the Simplified IMWG frailty index

• Have clinical laboratory values meeting defined range

• Patients of childbearing potential must agree to use adequate/highly effective contraception from the time of signing the informed consent form through 3 months after the last dose of study drug

Locations
Other Locations
Italy
IT-Ascoli Piceno-Ospedale Mazzoni [01-016]
RECRUITING
Ascoli Piceno
IT-Bari-A.O.U. Consorziale Policlinico - Medicina Interna [01-018]
NOT_YET_RECRUITING
Bari
IT-Bergamo-A.O. Papa Giovanni XXIII [01-003]
NOT_YET_RECRUITING
Bergamo
IT-Bologna-A.O.U. di Bologna - Policlinico S. Orsola Malpighi [01-004]
NOT_YET_RECRUITING
Bologna
IT-Bolzano-Ospedale di Bolzano - Azienda Sanitaria dell'Alto Adige [01-021]
NOT_YET_RECRUITING
Bolzano
IT-Como-Ospedale Classificato Valduce [01-104]
RECRUITING
Como
IT-Milano-Fondazione IRCCS Ca' Grande Ospedale Maggiore Policlinico [01-039]
NOT_YET_RECRUITING
Milan
IT-Milano-Ospedale S. Carlo Borromeo [01-105]
RECRUITING
Milan
IT-Novara-A.O.U. Maggiore della Carità [01-010]
RECRUITING
Novara
IT-Pescara-Azienda USL di Pescara P.O. dello Spirito Santo [01-053]
RECRUITING
Pescara
IT-Roma-ASL Roma 1 [01-101]
NOT_YET_RECRUITING
Roma
IT-Roma-Policlinico Umberto I - Università 'Sapienza' [01-013]
NOT_YET_RECRUITING
Roma
IT-Torino-A.O.U. Città della Salute e della Scienza di Torino-SSD Clinical trials [01-001]
NOT_YET_RECRUITING
Torino
IT-Varese-Ospedale di Circolo [01-111]
NOT_YET_RECRUITING
Varese
Netherlands
NL-Amsterdam-Vrije Universiteit Medical Center (VUMC) [02-007]
NOT_YET_RECRUITING
Amsterdam
NL-Arnhem-Rijnstate Hospital [02-009]
NOT_YET_RECRUITING
Arnhem
NL-Enschede-Medisch Spectrum Twente [02-024]
NOT_YET_RECRUITING
Enschede
NL-Groningen-University Medical Center Groningen [02-030]
NOT_YET_RECRUITING
Groningen
NL-Nieuwegein-S. Antonius Hospital [02-038]
NOT_YET_RECRUITING
Nieuwegein
NL-Schiedam-Franciscus Vlietland Hospital [02-049]
NOT_YET_RECRUITING
Schiedam
NL-Sittard-Geleen-Zuyderland Medical Center [02-058]
NOT_YET_RECRUITING
Sittard
NL-Den Haag-Haga Ziekenhuis [02-016]
NOT_YET_RECRUITING
The Hague
NL-Zwolle-Isala Klinieken [02-057]
NOT_YET_RECRUITING
Zwolle
Norway
NO-Oslo-Oslo University Hospital [23-007]
NOT_YET_RECRUITING
Oslo
NO-Tønsberg-Vestfold Hospital Trust [23-012]
NOT_YET_RECRUITING
Tønsberg
Spain
ES-Barcelona-H.U. Vall d'Hebrón [06-002]
NOT_YET_RECRUITING
Barcelona
ES-Las Palmas-H.U. de Gran Canaria Dr Negrín [06-030]
NOT_YET_RECRUITING
Las Palmas
ES-Murcia-H.U. Virgen de la Arrixaca [06-016]
RECRUITING
Murcia
ES-Salamanca-H.U. de Salamanca [06-021]
NOT_YET_RECRUITING
Salamanca
Contact Information
Primary
Clinical Trial Office
amministrazione@emnresearch.it
+390110243236
Time Frame
Start Date: 2025-12-12
Estimated Completion Date: 2034-02
Participants
Target number of participants: 150
Treatments
Experimental: Cohort 1
Tec-Dara
Experimental: Cohort 2
Tal-Dara
Related Therapeutic Areas
Sponsors
Leads: European Myeloma Network B.V.
Collaborators: Janssen Pharmaceutica N.V., Belgium, Nordic Myeloma Study Group, HOVON - Dutch Haemato-Oncology Association, PETHEMA Foundation, EMN Trial Office S.r.l. Impresa Sociale

This content was sourced from clinicaltrials.gov

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