A Randomized, Double-blind, Phase 3 Trial of Elesclomol (STA-4783) in Combination With Paclitaxel Versus Paclitaxel Alone for Treatment of Chemotherapy-Naïve Subjects With Stage IV Metastatic Melanoma (SYMMETRY)
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 入组人数
- 630
- 试验地点
- 99
- 主要终点
- Progression free survival
研究概览
简要总结
"Elesclomol (STA-4783), N-malonyl-bis (N'-methyl-N'-thiobenzoylhydrazide) is a new chemical entity with a novel structure. STA-4783 induces an oxidative stress response in cells. This response is characterized by increased production of gene families that protect against different cellular stresses, including excessive heat, the presence of reactive oxygen species such as oxygen radicals, or the presence of heavy metals.
Subjects will participate in up to 2 weeks of screening during which time they will complete all screening procedures. Eligible subjects who have not received any prior cytotoxic chemotherapeutic agent for melanoma will be randomized in a 1:1 ratio to receive either STA-4783 213 mg/m2 in combination with paclitaxel 80 mg/m2 or paclitaxel 80 mg/m2 alone.
One treatment cycle will consist of weekly treatments for 3 weeks, followed by a 1-week rest period. Cycles will be repeated every 4 weeks until disease progression. Tumor assessments will be performed every 8 weeks from the date of randomization or sooner if the Investigator suspects progression has occurred based on clinical signs and symptoms. "
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
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Histologically confirmed metastatic (Stage IV) melanoma of cutaneous origin
- •ECOG performance status of <=2
- •Measurable disease according to modified RECIST
- •Life expectancy of greater than 12 weeks
- •LDH <= 2.0 x ULN
- •Clinical lab values within protocol parameters.
- •At least 18 years old and able and willing to provide informed consent to participate
排除标准
- •Previous cytotoxic chemotherapy treatment for melanoma
- •Received more than one regimen of immunotherapy, kinase inhibitor, biologic therapy, vaccine or investigational non-chemotherapeutic treatment for melanoma.
- •Presence of brain metastases
- •Presence or history (<= 5 years) of a second malignancy other than nonmelanoma skin cancer or cervical carcinoma in situ
- •Female subjects who are pregnant or nursing
研究组 & 干预措施
1
Elesclomol (STA-4783) in Combination With Paclitaxel
干预措施: Elesclomol (STA-4783) (Drug)
2
Paclitaxel alone
干预措施: Paclitaxel (Drug)
结局指标
主要结局
Progression free survival
时间窗: June 2009
次要结局
- Overall Survival(December 2009)
- Clinical benefit rate(December 2009)
- Safety(December 2009)
- Pharmacokinetics(December 2009)
- Objective response rate(December 2009)
- Duration of objective response(December 2009)
