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IRD (ixazomib, lenalidomide, and dexamethasone) consolidation therapy after autologous peripheral hematopoietic stem cell transplantation for elderly multiple myeloma patients.

IRD (ixazomib, lenalidomide, and dexamethasone) consolidation therapy after autologous peripheral hematopoietic stem cell transplantation for elderly multiple myeloma patients. - IRD consolidation after ASCT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000039016
Enrollment
28
Registered
2019-12-28
Start date
2020-01-06
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

multiple myaloma

Interventions

4 cycles of IRD consolidation therapy will be administered. ixazomib 3mg at day 1,8, 15 on a 28-day cycle basis. lenalidomide 15mg at day 1-21 on a 28-day cycle basis. dexamathasone 20mg day 1, 8,

Sponsors

Tokyo-Kita Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Participants must sign the most current institutional review board (IRB)-approved informed consent form(ICF). 2) Multiple myeloma patients who received ASCT in 3 months and achieved partial response or better. 3) Age 65 - 74 years or <65 years who are not deemed appropriate for KRD consolidation therapy. 4) ECOG performance status 0-1. 5) Neutrophil >1000 and platelet >75000. 6) Serum GOT or GPT < 3.0 X upper limit of normal (ULN), and Serum total bilirubin < 1.5 ULN 7) Serum creatinine clearance > 30 ml/min.

Exclusion criteria

Exclusion criteria: 1) Peripheral neuropathy grade > 2 2) Uncontrolled diabetes. 3) Uncontrolled hypertension, arrhythmia, or heart failure. 4) Uncontrolled infectious diseases. 5) Uncontrolled psychiatric disorders. 6) Pregnant or lactating patients. 7) Allergic to ixazomib or lenalidomide. 8) Inability to comply with RevMmate. 9) Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study

Design outcomes

Primary

MeasureTime frame
Completion rate of 4 cycles of IRD consolidation therapy.

Countries

Japan

Contacts

Public ContactAkira Tanimura

Tokyo-kita Medical Center Department of Hematology

akiratan@jadecom.jp03-5963-3311

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026