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临床试验/NCT06771180
NCT06771180尚未招募2 期

Daratumumab, Bortezomib, Cyclophosphamide, and Dexamethasone Therapy for Patients with Rare Monoclonal Gammopathies of Renal Significance

Peking University People's Hospital0 个研究点目标入组 10 人开始时间: 2025年1月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
尚未招募
入组人数
10
主要终点
Rate of Hematologic Complete Response at the completion of 6 cycles

研究概览

简要总结

This is an open-label, multicenter, phase 2 study in subjects with newly diagnosed proliferative glomerulonephritis with monoclonal immunoglobulin deposits (PGNMIDs), OR light chain proximal tubulopathy (LCPT), OR thrombotic Microangiopathy (TMA), OR cryoglobulinemic glomerulonephritis, (CGGN), treated with daratumumab, bortezomib, cyclophosphamide, and dexamethasone.

详细描述

The current study aims to investigate daratumumab, bortezomib, cyclophosphamide, and dexamethasone regimen in patients with newly diagnosed PGNMIDs, LCPT, TMA, CGGN. Approximately 10 subjects will receive primary therapy with daratumumab-CyBorD. The primary endpoint is overall complete hematologic response (CHR) rate at 6 months.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Diagnosis of PGNMIDs, OR LCPT, OR TMA, OR CGGN.
  • Evidence of clonal plasma cell in bone marrow.
  • Neu≥ 1.0*10^9/L, HGB ≥70g/L, PLT ≥ 50*10^9/L.
  • Total bilirubin (TBil) ≤3×upper limit of normal (ULN); aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤3.0×ULN;
  • Informed consent explained to, understood by and signed by the patient.

排除标准

  • Prior therapy for MGRS, with the exception of equal or less than 160 mg dexamethasone (or equivalent corticosteroid)
  • Fulfill with the criteria of active multiple myeloma or active lymphoplasmacytic lymphoma.
  • Presence of other tumors which is/are in advanced malignant stage and has/have systemic metastasis;
  • Severe or persistent infection that cannot be effectively controlled;
  • Presence of severe autoimmune diseases or immunodeficiency disease;
  • Patients with active hepatitis B or hepatitis C ([HBVDNA+] or [HCVRNA+]); Patients with HIV infection or syphilis infection;
  • Any situations that the researchers believe will increase the risks for the subject or affect the results of the study.

研究组 & 干预措施

Dara-CyBorD

Experimental

Daratumumab Cyclophosphamide Bortezomib Dexamethasone

干预措施: Dara-CyBorD (Drug)

结局指标

主要结局

Rate of Hematologic Complete Response at the completion of 6 cycles

时间窗: 6 months

Hematologic complete response requires absence of monoclonal protein by immunofixation electrophoreses of both serum and urine as well as a normal FLC ratio (FLCr). CR is considered when FLCr was altered in favour of the non-amyloidogenic, uninvolved FLC (uFLC), even though the ratio may not have been normalised.

次要结局

  • Rate of Hematologic CR (Complete Response)+ VGPR (very good partial response) at the completion of 6 cyels(6 months)
  • Rate of Hematologic ORR (Overall Response, CR+VGPR+low-dFLC response+PR) at the completion of 6 cyels(6 months)
  • Renal response at 6 months(6 months)
  • MRD status at 6 months(6 months)
  • Renal Survival in 2 years(2 years)
  • Overall Survival in 2 years(2 years)
  • TRAEs(2 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jin Lu, MD

Dr

Peking University People's Hospital

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