Real-World Use of Selinexor, Daratumumab and Dexamethasone in Chinese Patients With Multiple Myeloma at First Relapse

Fu chengcheng PhD (Other)
Overall Status
Not yet recruiting ID

Study Details

Study Description

Brief Summary

This is a single-arm, prospective, non-interventional, real-world study to observe and evaluate the efficacy and safety of selinexor in combination with daratumumab and dexamethasone in patients with multiple myeloma at first relapse.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This is a non-interventional, prospective, observational post-marketing surveillance study of selinexor, daratumumab and dexamethasone in participants with multiple myeloma (MM).

    The study will assess the safety and effectiveness of selinexor in combination with daratumumab and dexamethasone (XDd) for first relapse MM patients under real-world conditions.

    The study will enroll approximately 34 participants. The data will be prospectively collected, at our center from medical files and recorded into electronic case report forms (e-CRFs).

    The overall duration of the study will be approximately 3 years. Data will be collected over and up to a 12 months-surveillance period (per participant) once enrolled.

    Study Design

    Study Type:
    Anticipated Enrollment :
    34 participants
    Observational Model:
    Time Perspective:
    Official Title:
    A Study of Real-World Use of Selinexor, Daratumumab and Dexamethasone in Chinese Patients With Multiple Myeloma at First Relapse
    Anticipated Study Start Date :
    Sep 20, 2022
    Anticipated Primary Completion Date :
    Jun 1, 2024
    Anticipated Study Completion Date :
    Jun 1, 2025

    Arms and Interventions

    Arm Intervention/Treatment
    Participants With Multiple Myeloma

    Participants with MM who are first relapsed and will start treatment with selinexor, daratumumab and dexamethasone in a real-world clinical practice setting will be observed prospectively for approximately up to 1 year.

    Outcome Measures

    Primary Outcome Measures

    1. Overall Response Rate (ORR) [28 days after the last therapy]

      ORR is defined as the percentage of participants with stringent complete response (sCR), complete response (CR), very good partial response (VGPR), or partial response (PR) based on the review of the myeloma response data assessed by International Myeloma Working Group (IMWG) criteria.

    Eligibility Criteria


    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Accepts Healthy Volunteers:
    Inclusion Criteria:
    1. According to the multiple myeloma diagnostic criteria of the International Myeloma Working Group (IMWG), there is the initial diagnosis of multiple myeloma.

    2. Subjects must have previously received 1 anti-myeloma regimens. Subjects must have documented disease progression

    3. Age ≥18 years;

    4. Life expectancy > 6 months;

    5. patients should provide available clinical case files and/or detailed records of medical history, diagnosis and treatment information, and cooperate with clinical management;

    6. Fertile women and men whose partner is of childbearing potential or pregnant should agree to practice complete abstinence or to use a condom during therapy and dose interruptions and for 90 days after the last treatment.

    Exclusion Criteria:
    1. Patients who are contraindicated as per product label of XDd;

    2. Known positive for HIV or active hepatitis B or C or other infectious diseases;

    3. Pregnancy or lactation;

    4. Patients with a history of malignant tumor that may affect the implementation or results analysis of this study (except cured basal cell carcinoma of the skin, carcinoma in situ of the cervix, carcinoma in situ of the breast, intramucosal carcinoma of the gastrointestinal tract in situ, and localized prostate cancer);

    5. Any other medical condition, including mental illness or substance abuse, deemed by the investigator(s) to likely interfere with the patient's ability to sign informed consent, cooperate and participate in the study, or interfere with the interpretation of the results;

    6. Patients who are unsuitable for this study judged by clinicians.

    Contacts and Locations


    No locations specified.

    Sponsors and Collaborators

    • Fu chengcheng PhD


    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information


    None provided.
    Responsible Party:
    Fu chengcheng PhD, Principal Investigator, The First Affiliated Hospital of Soochow University Identifier:
    Other Study ID Numbers:
    • SDd-MM06
    First Posted:
    Sep 29, 2022
    Last Update Posted:
    Sep 29, 2022
    Last Verified:
    Sep 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    Studies a U.S. FDA-regulated Device Product:
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 29, 2022