Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:26 AM
Ignite Modification Date:
2025-12-25 @ 2:26 AM
NCT ID:
NCT02481934
Eligibility Criteria:
Inclusion Criteria:
* Subjects between 20 and 80 years old
* With multiple myeloma in 2nd or later relapse or showing resistance after 2 treatment lines
* Eastern Cooperative Oncology Group (ECOG) ≤ 2
* Life expectancy greater than six months
* Creatinine clearance rate more than 30 ml / min
* Subjects who have received at least 4 cycles of rescue treatment under the procedures of the 12 de Octubre Hospital (rescue treatment will vary depending on previous anti-myeloma treatment). After treatment, patients must have shown chemosensitivity and disease stabilization.
* Will be included subjects with partial response or stable disease (for at least 2 cycles) after 75% of planned rescue treatment or patients at subclinical progression (defined as an increase of monoclonal component ≥ 25%) at any time of rescue treatment. Subjects have to show tolerance to rescue treatment, without G3/4 adverse effects, if G1/2 adverse effects exist they must be analyzed immediately before starting reinfusion program.
* Subjects have to agree to participate in the trial and they have to sign informed consent.
Exclusion Criteria:
* Subjects with clinical progression or complete response will not be included.
* Any of the following abnormal laboratory results:
Absolute Neutrophil Count \< 1000/ µL Platelets Count \< 50000/ µL in those patients with bone marrow infiltration lower than 50% Measured creatinine clearance \<30 ml/min Hemoglobin level ≤ 8 g/dL Peripheral neuropathy ≥ Grade 2
* Subjects have received allogeneic stem cell transplant.
* Subjects with heart disease which compromises patient's life or protocol accomplishment.
* Subjects with past clinical history of malignant disease within 3 years (exceptions are squamous or basal cell carcinoma).
* Subjects receiving another investigational drug or having received investigational drug within 30 days before screening.
* Subjects who require chronic steroid or immunosuppressive treatment.
* Any condition, including abnormally laboratory results, that might compromise the patient´s life if he participate in this study.
* Any concurrent medical condition, abnormally laboratory results or any psychological disorder that prevent the patient to sign the informed consent.
* Pregnant or fertile women.
* Patients known to be seropositive for human immunodeficiency virus (VIH) or having active hepatitis A, B or C.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
20 Years
Maximum Age:
80 Years
Study:
NCT02481934
Study Brief:
Protocol Section:
NCT02481934