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临床试验/NCT00538668
NCT00538668已完成1 期

Radioimmunotherapy Phase I Dose-Escalation Studies in Prostate Cancer Using 177Lu-J591 Antibody: Dose Fractionation Regimen

Weill Medical College of Cornell University1 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2007年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
55
试验地点
1
主要终点
Define the PK and dosimetry of 177Lu-J591

研究概览

简要总结

The purpose of this study is to test the safety of the experimental drug, 177Lu-J591 and see what effects (good and bad) it has on your prostate cancer. Another purpose is to find the highest dose of the drug that can be given without causing severe side effects.

详细描述

Study Design: We plan to perform a phase I dose-escalation study. The trial is designed to determine the cumulative MTD in a FDR in which 177Lu-J591 will be given in 2 doses, 2 weeks apart. The dose escalation will start at 20 mCi/m2 and escalate in increments of 5 mCi/m2 to 55 mCi/m2 in up to 8 cohorts.We plan to recruit a maximum of 68 subjects in this trial.

Specific Aims: 1. Determine the cumulative MTD of 177Lu-J591 in a 2 week dose-fractionation regimen.

  1. Perform imaging and pharmacokinetic (PK) studies with 177Lu-J591 in order to define the PK and dosimetry of 177Lu-J591 3. Determine the myelotoxicity of fractionated dose of 177Lu-J591 4. Monitor biochemical (PSA) and/or measurable disease response and duration.

Following the administration of 177Lu-J591 mAb on day 0, blood samples may be obtained at 10 min, 1, 2, 4 hrs, days 1, once during days 3-6, day 7 and 14. In addition, total body images may be obtained on day 0 at 1-4 hours after study treatment, day 1, once during days 3-6, days 7 and 14 using a gamma camera. (Amendment dated 15 July 2009: As investigators have gained ample information from the initial cohorts, PK and 177Lu-J591 imaging studies (other than the day 6-8 scan) will be considered optional.) Patients will be followed for a minimum of 12 weeks after the 2nd dose of 177Lu-J591 (total 14 weeks) or until toxicities resolve, disease progression or administration of alternative therapy for the patient¿s prostate cancer. Various clinical and laboratory evaluations will be performed during the first week and then every week until 12 weeks. These include, blood chemistries, CBCs, serum PSA levels, etc. If the patient¿s disease is stable or responding at 12 weeks after his last dose, he will continue to be followed until progression of disease. During the long-term follow-up, the patient¿s PSA will be monitored at least every 6 weeks and CT/bone scans will be evaluated at least every 18 weeks until disease progression.

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

年龄范围
21 Years 至 85 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

1

Experimental

20 mCi/m2 of 177Lu-J591 will be given in 2 doses, 2 weeks apart.

干预措施: 117Lu-J591 (Drug)

2

Experimental

25 mCi/m2 of 177Lu-J591 will be given in 2 doses, 2 weeks apart.

干预措施: 117Lu-J591 (Drug)

3

Experimental

30 mCi/m2 of 177Lu-J591 will be given in 2 doses, 2 weeks apart.

干预措施: 117Lu-J591 (Drug)

4

Experimental

35 mCi/m2 of 177Lu-J591 will be given in 2 doses, 2 weeks apart.

干预措施: 117Lu-J591 (Drug)

5

Experimental

40 mCi/m2 of 177Lu-J591 will be given in 2 doses, 2 weeks apart.

干预措施: 117Lu-J591 (Drug)

6

Experimental

45 mCi/m2 of 177Lu-J591 will be given in 2 doses, 2 weeks apart.

干预措施: 117Lu-J591 (Drug)

7

Experimental

50 mCi/m2 of 177Lu-J591 will be given in 2 doses, 2 weeks apart.

干预措施: 117Lu-J591 (Drug)

8

Experimental

55 mCi/m2 of 177Lu-J591 will be given in 2 doses, 2 weeks apart.

干预措施: 117Lu-J591 (Drug)

9

Experimental

25 mCi/m2 of 177Lu-J591 will be given every 2 weeks.

干预措施: 117Lu-J591 (Drug)

结局指标

主要结局

Define the PK and dosimetry of 177Lu-J591

时间窗: Perform imaging and pharmacokinetic (PK) sampling during the first two weeks of treatment.

Determine the myelotoxicity of fractionated dose of 177Lu-J591

时间窗: Lab tests will be performed weekly.

Define the preliminary efficacy (response rate) of 177Lu-J591

时间窗: PSA will be evaluated at baseline and weeks 6, 10 and 14. Scan will be perfoemed at baseline and week 14.

Determine the cumulative maximum tolerated dose of 177Lu-J591 in a 2 week dose-fractionation regimen.

时间窗: Will be determined baesd on toxicity experienced by patients at each dose level.

次要结局

  • Monitor biochemical (PSA) and/or measurable disease response and duration.(PSA will be evaluated at baseline and weeks 6, 10 and 14. Scan will be perfoemed at baseline and week 14.)
  • Estimate radiation dosimetry of 177Lu-J591 and correlate toxicity with radiation dosimetry.(Total body images will be obtained on day 0 at 1-4 hours after treatment, day 1, once during days 3-6, days 7 and 14)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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