Ixazomib, Lenalidomide, and Combination for Maintenance in NDMM Patients

NCT04217967 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 211

Last updated 2024-08-01

No results posted yet for this study

Summary

The purpose of this study is to evaluate the real-world efficacy and safety of ixazomib, lenalidomide, or ixazomib in combination with lenalidomide as maintenance therapy in patients with newly diagnosed multiple myeloma in China.

Conditions

Interventions

DRUG

Ixazomib

the ixazomib group uses ixazomib as the comparator group, the combination group receives both lenalidomide and ixazomib as the experimental group

DRUG

Lenalidomide

the lenalidomide group uses lenalidomide as comparitor group and the combination group receives both lenalidomide and ixazomib

Sponsors & Collaborators

  • Peking University Third Hospital

    collaborator OTHER
  • Beijing Jishuitan Hospital

    collaborator OTHER
  • Beijing Chao Yang Hospital

    collaborator OTHER
  • Xuanwu Hospital, Beijing

    collaborator OTHER
  • Peking University First Hospital

    collaborator OTHER
  • Jilin Provincial Tumor Hospital

    collaborator OTHER
  • Second Hospital of Shanxi Medical University

    collaborator OTHER
  • The First Affiliated Hospital of Shanxi Medical University

    collaborator OTHER
  • Tianjin Medical University General Hospital

    collaborator OTHER
  • The First Affiliated Hospital of Anhui Medical University

    collaborator OTHER
  • Shanxi Bethune Hospital

    collaborator OTHER
  • Beijing Hospital

    collaborator OTHER_GOV
  • Peking Union Medical College Hospital

    lead OTHER

Principal Investigators

  • Junling Zhuang, MD · Peking Union Medical College, department of hematology

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-24
Primary Completion
2024-06-30
Completion
2024-06-30
FDA Drug
Yes

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04217967 on ClinicalTrials.gov