A Study to Learn How Patients With Triple Class Refractory Multiple Myeloma (TCR-MM) Are Treated in Italian Centers for Blood Related Diseases

NCT ID: NCT05742217

Last Updated: 2026-02-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

250 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-05-26

Study Completion Date

2026-05-31

Brief Summary

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Multiple myeloma (MM) is a type of cancer of the white blood cells, called plasma cells. These plasma cells help in fighting infections.

TCR-MM is when the cancer does not get treated with the 3 main classes of medicines used to treat this disease.

The purpose of this study is to learn about the present clinical practice in Italy and describe the standard of care that will be given to patients with TCR-MM, and their treatment costs, in around 25 centers who treat patients with blood diseases.

Standard of care (SoC) is the treatment that is accepted as a proper treatment for a certain type of disease and that is widely used by doctors.

The study is seeking for participants who are:

* 18 years of age or older
* Confirmed to have MM
* do not show any response when treated with the 3 main classes of medicines used to treat MM Data of participants who received the TCR treatment between 01 December 2021 and 31 May will be collected.

The main data source for the study will be the patient medical record. No clinical visits, examinations, or procedures are required as part of this study.

Detailed Description

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In Italy, MM represents 1.6 percent of all cancers diagnosed in men and 1.5 percent of those diagnosed in women. The 2020 Italian epidemiological data show 5759 new diagnosis of MM. Most MM patients relapse or become refractory to various therapeutic approaches and typically cycle through many lines of treatment. Survival among patients refractory to newer therapies, including PIs, IMiDs and anti-CD38 mAbs, is very low and measured in months. An Italian real life data collection is important to analyse the current therapeutic approaches in TCR patients and the costs incurred by the therapy based on the different treatments.

Conditions

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Relapse Multiple Myeloma Refractory Multiple Myeloma

Study Design

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Observational Model Type

OTHER

Study Time Perspective

OTHER

Eligibility Criteria

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Inclusion Criteria

* Age ≥18 years
* Diagnosis of MM confirmed using International Myeloma Working Group (IMWG) criteria
* Patients are TCR defined as being refractory to all the 3 following classes: at least 1IMiD, at least 1PI and at least 1 anti-CD38 mA
* Relapsed/refractory to last anti-MM regimen prior to first treatment after TCR
* Started anti-MM treatment after TCR MM eligibility
* Eastern Cooperative Oncology Group (ECOG) performance status ≤2 (at the date of first dose of first treatment after TCR MM eligibility, or no longer than 6 months prior to this date)
* Evidence of a personally signed and dated informed consent document indicating that the patient (or a legally acceptable representative) has been informed of all pertinent aspects of the study. Signed Patient informed consent and Privacy consent documents

Exclusion Criteria

* Suffering from Smoldering MM
* Suffering from Plasma cell leukemia
* Suffering from amyloidosis
* Suffering from active Graft versus host disease (GvHD)
* Suffering from any other active malignancy within 3 years prior to enrollment, except for adequately treated basal cell or squamous cell skin cancer or carcinoma in situ
* Patients whose first treatment after becoming TCR was part of a clinical trial
* Participation in Elranatamab EAP
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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A.O.U. - Ospedali Riuniti di Ancona

Torrette, Aviano, Italy

Site Status

A.O.U. Policlinico S.Orsola Malpighi

Bologna, BO, Italy

Site Status

"IRCCS "" Casa Sollievo della Sofferenza""tOpera di San Pio da Pietrelcina U.O.C di Ematologia"

San Giovanni Rotondo, Foggia, Italy

Site Status

AOU Policlinico Umberto I

Rome, Lazio, Italy

Site Status

Fondazione IRCCS Policlinico Sa Matteo U.O.C. Ematologia

Pavia, Lombardy, Italy

Site Status

A.O.U Policlinico G. Rodolico S. Marco

Catania, Sicily, Italy

Site Status

A.O.U. Policlinico Paolo Giaccone

Palermo, Sicily, Italy

Site Status

A.O.O.R. Villa Sofia Cervello, U.O. Oncoematologia

Palermo, Sicily, Italy

Site Status

Azienda Ospedaliera Universitaria Careggi

Florence, , Italy

Site Status

IRST, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori

Meldola (FC), , Italy

Site Status

A.O.U. Policlinico Università degli Studi di Napoli "Federico II"

Napoli, , Italy

Site Status

Azienda Ospedaliero-Universitaria Maggiore della Carita

Novara, , Italy

Site Status

Azienda Ospedaliero - Universitaria Di Parma

Parma, , Italy

Site Status

Ospedale Civile dello Spirito Santo

Pescara, , Italy

Site Status

Arcispedale Santa Maria Nuova

Reggio Emilia, , Italy

Site Status

AUSL della Romagna P.O. Ospedale Infermi U.O. di Oncologia

Rimini, , Italy

Site Status

Irccs Crob

Rionero in Vulture, , Italy

Site Status

San Giovanni Di Dio E Ruggi D'Aragona Hospital

Salerno, , Italy

Site Status

Busto Arsizio Hospital

Varese, , Italy

Site Status

Countries

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Italy

Related Links

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https://pmiform.com/clinical-trial-info-request?StudyID=C1071025

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Other Identifiers

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MUST

Identifier Type: OTHER

Identifier Source: secondary_id

C1071025

Identifier Type: -

Identifier Source: org_study_id

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