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临床试验/NCT04538833
NCT04538833撤回2 期

Monosialoganglioside in the Treatment of Neurotoxicity Induced by Albumin-bound Paclitaxel : a Multicenter, Double-blind, Randomized Controlled Phase II Clinical Trial

Henan Cancer Hospital1 个研究点 分布在 1 个国家开始时间: 2020年9月9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
撤回
试验地点
1
主要终点
FACT-Ntx score

研究概览

简要总结

Taxane-induced peripheral neuropathy (TIPN) caused by albumin-bound paclitaxel is a dose-limiting toxicity. The main symptoms of discomfort are numbness, tingling, and burning sensations in the glove-sock-like distribution of the limbs. At present, there are few effective methods for clinical treatment of TIPN, and there is no widely agreed consensus on effective treatment in the world. Therefore, it is of great clinical significance and practical value to carry out clinical research to explore drugs to relieve TIPN.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Female patients diagnosed with early breast cancer by histology;
  • Age ≥18 years old and ≤75 years old
  • At least 1-2 cycles of standard chemotherapy regimens containing albumin-bound paclitaxel were used in adjuvant / neoadjuvant chemotherapy regimens, The FACT-Ntx score was ≤ 37, and the remaining chemotherapy cycles were at least 2 cycles. the standard regimen included: a, albumin paclitaxel one-week regimen; b, albumin paclitaxel 3-week regimen. Platinum and other types of neurotoxic drugs shall not be included in the regimen.
  • ECOG score of the patient is ≤1;
  • Expected survival time ≥ 3 months;
  • The function level of main organs must meet the following requirements (no blood transfusion and no use of leukocyte or platelet rising drugs within 2 weeks before screening) Blood routine: neutrophil (ANC) ≥ 1.5x 10^9 / L; platelet (PLT) ≥ 90x10^9 / L; hemoglobin (Hb) ≥ 90g / L; Blood biochemical total bilirubin (TBIL) ≤ 1.5xULN; alanine aminotransferase (AST) and aspartate aminotransferase (AST) not exceeding 2×ULN; blood urea nitrogen (BUN) and creatinine (CR) below 1.5 × ULN;
  • FACT-Ntx score is 44 points before the adjuvant / neoadjuvant chemotherapy was given;
  • Sign the informed consent.

排除标准

  • Other pathological symptoms or diseases may affect the assessment of adverse neurotoxicity before enrollment
  • Patients receiving other medications may cause similar adverse neurotoxic effects within 4 weeks before treatment with this regimen, or they may also receive neurotoxic medications at the same time. Including paclitaxel or analogues; vinca alkaloids or analogues; platinums or analogues; cytarabine, thalidomide, bortezomib or cabazine; other drugs or treatments may cause peripheral neurotoxicity;
  • Patients with poor overall condition and ECOG score> 1;
  • pregnant or lactating women;
  • Patients who also suffer from other neurological abnormalities cannot accurately record the occurrence and severity of neurotoxicity;
  • The patient is known to be allergic to the test drug or excipient ingredients of these products;
  • Patients with hereditary abnormalities of glucose and lipid metabolism (gangliopathies, such as idiopathic and retinopathy of triad families);
  • Patients not suitable for ganglioside treatment;
  • Patients with severe concurrent diseases may endanger safety and interfere with scheduled treatment, or the combination of diseases may affect the completion of the study, depending on the judgment of the investigator.
  • Patients with a clear history of neurological or mental disorders, including epilepsy or dementia.

研究组 & 干预措施

monosialic ganglioside

Experimental

On the days -1, 1, and 2 of albumin-bound paclitaxel application, 80 mg of monosialic ganglioside were applied (monosialic ganglioside was a single infusion)

干预措施: monosialic gangliosides (Drug)

Placebo

Placebo Comparator

The control group received placebo on days -1, 1, and 2 of albumin-bound paclitaxel application, (placebo as a single infusion)

干预措施: Placebo (Other)

结局指标

主要结局

FACT-Ntx score

时间窗: 2 weeks after chemotherapy

The FACT-Ntx subscale includes 11 items, each of which is divided into 5 scoring levels: 0, 1, 2, 3, 4, and a total score of 44. Higher scores indicate lower side effects

次要结局

  • FACT-Taxane score(During chemotherapy, and 2 weeks, 3 months, 6 months, and 12 months after chemotherapy)
  • CTCAE Version 4.0 score(During chemotherapy, and 2 weeks, 3 months, 6 months, and 12 months after chemotherapy)
  • FACT-Ntx score(3 months, 6 months, and 12 months after chemotherapy)
  • FACT-G score(During chemotherapy, and 2 weeks, 3 months, 6 months, and 12 months after chemotherapy)

研究者

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

Zhenzhen Liu

Director

Henan Cancer Hospital

研究点 (1)

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