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NCT Number: NCT06697483

Risk Stratification and MRD-driven Maintenance for MM After ASCT

This study evaluates the maintenance strategy based on risk stratification and MRD status after stem cell transplantation.

This is a single-arm, multicenter, prospective study. Participants who are R2-ISS 1,2 and MRD negative receive the single drug lenalidomide maintenance. In other circumstances, for example, patients who are R2-ISS 3 or 4 will receive daratumumab combined with lenalidomide regardless of MRD status, while patients with MRD positivity will also receive daratumumab plus lenalidomide maintenance.

Recruiting

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Newly diagnosed multiple myeloma with a history of a minimum of 4 cycles of induction therapy, have received high-dose therapy (HDT) and autologous stem cell transplantation (ASCT) within 12 months of the start of induction therapy, and be within 6 months of ASCT.
  • Must have a partial response (PR) or better response before maintenance.
  • Must have an Eastern Cooperative Oncology Group performance status score of 0, 1, or 2.
  • This study allows for post-ASCT consolidation therapy.
  • ANC ≥ 1.0 x 10^9/L, Hb ≥ 85 g/L PLT ≥ 75 x 10^9/L (if BMPC < 50%) or PLT ≥ 50 x 10^9/L (if BMPC ≥ 50%).
  • No active infection.
  • a).TBIL<1.5 x upper limit of normal (ULN) (<3 x ULN in patients with Gilbert's syndrome); b).AST and ALT <3 x ULN.; c. Creatinine clearance ≥ 45mL/min.

Exclusion criteria

  • Must not refractory or non-tolerate to lenalidomide in Arm A.
  • Must not refractory or non-tolerate to lenalidomide and daratumumab in Arm B.
  • Must not have progressed on multiple myeloma (MM) therapy before screening
  • Chronic obstructive pulmonary disease (COPD) with FEV1 less than 50 % of predicted normal;
  • Have known moderate or severe persistent asthma within the past 2 years or current uncontrolled asthma of any classification
  • History of stroke or serious thrombotic event within 12 months prior to screening.

Treatment and study plan

Daratumumab

Drug

Patients who are R2-ISS 3 or 4 OR MRD (Minimal Residual Disease) positivity will receive daratumumab plus lenalidomide maintenance.

Lenalidomide

Drug

Patients are R2-ISS 1,2 and MRD (Minimal Residual Disease) negative after autologous stem cell transplantation.

Patients will receive the single drug lenalidomide maintenance.

Primary outcomes

  1. MRD (Minimal Residual Disease) status at 12 months after maintenance

    Time frame: 12 months

    Bone marrow minimal residual disease status at 12 months after maintenance

Secondary outcomes

  1. CR+VGPR

    Time frame: 12 months

    complete response plus very good partial response at 12 months from maintenance

  2. Estimated 3 year-PFS

    Time frame: 3 years

    Estimated 3 year progression free survival

  3. Estimated 3 year OS

    Time frame: 3 years

    Estimated 3 year overall survival

  4. TRAEs

    Time frame: 3 years

    Treatment related adverse events

Study contacts

Contact information is provided by the study sponsor or research team.

Yang Dr, M.D.

CONTACT

[email protected]

+86-10-88326542

Sponsors and collaborators

Lead sponsor

Peking University People's Hospital

Other

Registry information

Official study title

Risk Stratification and MRD-driven Maintenance for Multiple Myeloma After Autologous Stem Cell Transplantation

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Nov 20, 2024
Registry last updated
Nov 25, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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