GAIRI: Gazyva Infusion Reaction Investigation

Sponsor
Healthy Future (Other)
Overall Status
Recruiting
CT.gov ID
NCT03529227
Collaborator
(none)
104
2
85
52
0.6

Study Details

Study Description

Brief Summary

The study evaluate safety and effectiveness of chlorambucil and obinutuzumab in routine clinical practice in patients with chronic lymphatic leukemia and with certain comorbidities (any cardiac pathology, diabetes mellitus (DM), kidney pathology or cytopenia), whom obinutuzumab & chlorambucil have been applied according to indications before enrollment in the study.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    MRD (Minimal residual disease) evaluation was chosen as a primary measure outcome as it is considered as prognostic marker for long-term progression freee survival (PFS) and as a potential therapeutic goal in chronic lymphocytic leukemia/ CLL .

    Minimal residual disease (MRD-negative) is assessed in the clinic by 8-color flow cytometry giving the sensitivity level of MRD detection 10-5; MRD is measured in real clinical practice at this clinical center according to National recommendations in diagnostics and treatment of lymphoproliferative disorders.

    To achieve study objectives medical patients' charts will be analyzed retrospectively. In the frame of this program 104 patients' charts treated in defined clinical site, are planned to be analyzed. This number of patients corresponds to the patient flow with this pathology at a defined clinical site for 1 years.

    Data collection is considered to be retrospective as data will be transferred to e-CRF from patient medical charts. During this study no further specific extra procedures for data gathering is expected.

    But since patients included in the study will be at the center of ongoing therapy, the study was called a prospective.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    104 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Prospective One-center Open Label Observational Efficacy & Safety Study of Chlorambucil & Obinutuzumab in Treatment of Unfit Patients With Untreated Chronic Lympho Leukemia With Comorbidities
    Actual Study Start Date :
    Mar 31, 2018
    Anticipated Primary Completion Date :
    Aug 31, 2024
    Anticipated Study Completion Date :
    Apr 30, 2025

    Outcome Measures

    Primary Outcome Measures

    1. MRD status of CLL patients with comorbidities [3 months after the last dose of study treatment]

      Number of patients with positive and negative MRD status

    Secondary Outcome Measures

    1. Response Rate (ORR) [3 months after last dose administration]

      Frequency of the overall response in patients with CLL using the Chlorambucil + Obinutuzumab (G-Clb) therapy regimen (N,%)

    2. Progression free survival (PFS) by the Kaplan-Meier method [3 months after last dose administration]

      Time to full remission in patients with CLL using Chlorambucil + Obinutuzumab (G-Clb) therapy regimen (month) calculated by the Kaplan-Meier method

    3. Duration of response (DOR) by the Kaplan-Meier method [3 months after last dose administration]

      Time to partial remission in patients with CLL using Chlorambucil + Obinutuzumab (G-Clb) therapy regimen (month) calculated by the Kaplan-Meier method

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. CD20+/ (cluster of differentiation antigen 20 positive) B-CLL pts on the 1st line treatment therapy, whom have been already applied Obinutuzumab and chlorambucil

    2. Age ≥ 18 years.

    3. Eastern Cooperative Oncology Group Scale (ECOG) 0-2.

    4. Total Chronic Illness Resources Survey scale (CIRS) score >6 or creatinine clearance <70 ml/min or both for patients ≥ 18 years old or all CLL pts ≥ 75 years old

    5. Any cardiac pathology/ diabetes mellitus/ kidney pathology/ cytopenia (Hb <100 g/l, Platelets < 100 x 109/l)

    6. Life expectancy more than 6 months according to the physician's opinion.

    7. Signed informed consent that allow personal data and data that refer to patient confidentiality processing

    Exclusion Criteria:

    The refusal of the patient to participate in the observational study and the withdrawal of informed consent that allow processing of personal data and data that refer to patient confidentiality.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The State Budgetary Moscow Healthcare Institution Clinical Hospital named after S.P. Botkin of Moscow Health Department". Moscow Russian Federation 125284
    2 The State Budgetary Moscow Healthcare Institution Clinical Hospital named after S.P. Botkin of Moscow Health Department Moscow Russian Federation 125284

    Sponsors and Collaborators

    • Healthy Future

    Investigators

    • Principal Investigator: Eugeny A Nikitin, MD, "The State Budgetary Moscow Healthcare Institution Clinical Hospital named after S.P. Botkin of Moscow Health Department"

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Healthy Future
    ClinicalTrials.gov Identifier:
    NCT03529227
    Other Study ID Numbers:
    • ML40194
    First Posted:
    May 18, 2018
    Last Update Posted:
    Feb 14, 2022
    Last Verified:
    Feb 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Healthy Future
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 14, 2022