Observational study on treatments for relapsed multiple myeloma

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study is a multicenter observational analysis focusing on patients with relapsed and refractory multiple myeloma who have previously undergone treatment with anti-CD38 monoclonal antibodies and immunomodulatory drugs (IMIDs). It aims to evaluate the effectiveness of on-label treatment regimens in these patients. The study includes both retrospective and prospective data collection to assess patient outcomes and treatment responses. Participants must be at least 18 years old and provide informed consent for data review.

Why it matters

Who can join: the full rules

Inclusion Criteria:

Phase I

* Patients with RRMM after therapy with anti-CD38 MoAb plus IMIDS started on therapy with PVD scheme
* Patients aged ≥ 18 years
* Patients able to understand and voluntarily sign an informed consent and be willing to consent to the review of clinical data

Phase II

* Patients with RRMM after first-line therapy with anti-CD38 MoAb plus IMIDS started on therapy with on-label schemes
* Patients aged ≥ 18 years
* Patients able to understand and voluntarily sign an informed consent and be willing to consent to the review of clinical data

Exclusion Criteria:

* Patients not willing to consent to review of clinical data

Where it's running

• Irccs San Matteo Pavia
  Pavia, Pv, Italy Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.