A Non-Randomised, Multicentre, Phase II Clinical Study of CP-4055 in Chemotherapy-Naïve Patients With Metastatic Malignant Melanoma
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 42
- 试验地点
- 6
- 主要终点
- Objective tumour response
研究概览
简要总结
Previously untreated patients with malignant melanoma receive a new chemotherapy drug currently under development. CP-4055 is given intravenously on days 1-5 every four weeks until complete response or disease progression.
详细描述
This is an international multicentre phase II clinical study conducted in the USA and Europe. Previously untreated patients over 18 years, with metastatic malignant melanoma are eligible for inclusion if they fulfil all inclusion- and exclusion criteria. 16 or 42 patients will be enrolled in Pittsburgh USA, Lund Sweden and Oslo Norway.
The new development drug CP-4055 is administered for five consecutive days (Day 1 to 5) in a 4 week schedule (one cycle). The dose is 200 mg/m2/day.
A patient will continue treatment until complete response or until (s)he is withdrawn from the Clinical Study because of disease progression, unacceptable toxicity or any other reason described in the clinical study protocol.
Efficacy is assessed at baseline and end of every second cycle with CT or MRI.
Safety assessments are done at each visit. Blood samples are taken and haematological and biochemical parameters are assessed for safety.
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
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with histologically or cytologically confirmed stage IV or unresectable stage III non-ocular malignant melanoma who have not undergone prior chemotherapy for the treatment of melanoma (chemotherapy-naïve)
- •Measurable disease according to Response Criteria in Solid Tumours (RECIST)
- •Performance Status 0 - 2 according to ECOG (Eastern Cooperative Oncology Group) Performance Status
- •Age 18 years or more
- •Life expectancy > 3 months
- •Signed informed consent
- •Adequate haematological and biological functions:
- •Bone marrow function:
- •Neutrophils ≥ 1.5 x 10^9/L
- •Platelets ≥ 100 x 10^9/L
- •Hemoglobin (Hb) ≥ 10 g/dL
- •Hepatic function:
- •AST/ALT ≤ 2.5 times institutional upper limit of normal (ULN). If liver metastases, ≤ 5 times institutional ULN.
- •Serum bilirubin and alkaline phosphatase ≤ 1.5 times institutional ULN
- •Renal function:
- •Creatinine ≤ 1.5 times institutional ULN
排除标准
- •Known brain metastases
- •Diagnosis of ocular malignant melanoma
- •Radiotherapy to more than 30% of bone marrow
- •Participation in another therapeutic clinical study within 30 days of enrolment or during this clinical study
- •Prior immunotherapy and/or chemotherapy for the treatment of melanoma
- •Requirement of concomitant treatment with a non-permitted medication:
- •Alternative drugs
- •High doses of vitamins
- •History of allergic reactions to Ara-C or egg
- •Presence of any serious concomitant systemic disorders incompatible with the clinical study (e.g. uncontrolled intercurrent illness including ongoing or active infection)
- •Presence of any significant central nervous system or psychiatric disorder(s) that would hamper the patient's compliance
- •Pregnancy, breastfeeding, or absence of adequate contraception for both male and female fertile patients
- •Known positive status for HIV and/or hepatitis B or C
- •Drug and/or alcohol abuse
- •Any reason why, in the Investigator's opinion, the patient should not participate
结局指标
主要结局
Objective tumour response
次要结局
- Time to progression
- Duration of tumour response
- Safety and tolerability of treatment