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Bortezomib plus dexamethasone in monoclonal gammopathy of renal significance

Bortezomib plus dexamethasone in monoclonal gammopathy of renal significance

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026355
Enrollment
Unknown
Registered
2019-10-02
Start date
2019-10-02
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

multiple myeloma

Interventions

1:Bortezomib plus dexamethasone +general kindey therapy
2:general kindey therapy

Sponsors

The First Affiliated Hospital, Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years. 2. MGRS according to the updated IKMGRG diagnostic criteria 2018. 3. EGCO 0-3 4. Estimated survival times over 6 months. 5. Meet the pregnancy prevention requirements: not of childbearing potential or agree to practice effective barrier contraception during the entire study treatment period and through 90 days after the last dose of study drug. 6. Able to provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Received other clinical trials for multiple myeloma within three months. 2. Prior or concurrent invasive malignancies. 3. Active systemic infection or any other medical or psychiatric condition which, in the opinion of the investigator, contraindicates the participant's participation in this study.

Design outcomes

Primary

MeasureTime frame
hemotological response rate;

Secondary

MeasureTime frame
organ response rate;toxicity;

Countries

China

Contacts

Public ContactJuan Li

The First Affiliated Hospital, Sun Yat-Sen University

hbh_st@126.com+86 13719209240

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026