NCT03773055终止2 期
A Multicenter, Double-blind, Randomized, Placebo-controlled Parallel Group Trial to Investigate the Proof of Concept of NPC-06 in Patients With Neuropathic Pain in Cancer
Nobelpharma1 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2019年4月3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
- 终止
- 发起方
- 入组人数
- 7
- 试验地点
- 1
- 主要终点
- Improvement of Numeric Rating Scale (NRS) score within 2 hours after administration
研究概览
简要总结
The purpose of this trial is to investigate the efficiency of pain relief and the safety of NPC-06 for the neuropathic pain associated with cancer, in addition to explore the effective concentration of NPC-06.
详细描述
The eligible patients will be randomized into three groups, and will receive NPC-06 (high dose), NPC-06 (low dose) or placebo once a day for 7 days.
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
- 16 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •16 years old or greater at the time of informed consent
- •Both genders
- •Patients who can admit to hospital for all assessment duration from first administration until the next day of final administration. (including the hospitalized patient )
- •Patients who are diagnosed and informed as cancer (including sarcoma, lymphoma and multiple myeloma)
- •Patients who are diagnosed as neuropathic pain by neurological examination and imaging findings
- •Patients who NRS score of average persistent pain is higher than 4, even they were treated with level 3 of WHO three-step analgesic ladder at the observation period.
- •Patients who NRS score at the time of first administration and NRS score of persistent pain in the past 24 hours are higher than
- •Patients who average number of daily rescue medication use during observation period is less than
- •Patients who are predicted to survive longer than 3 month.
- •Patients who ECOG Performance Status (PS) score is 0 to
- •Patients who (or whose legally acceptable representative if the patient is underage) provide a written consent at their own will with a full understanding after receiving a sufficient explanation on participation in the study
排除标准
- •Patients who can not evaluate NRS by themselves.
- •Patients who have leukemia as a complication.
- •Patients who have a primary brain neoplasm or a metastatic brain neoplasm as a complication.
- •Patients who have epilepsy, serious psychiatric or neurological disease ( i. e. dementia, Parkinson disease or schizophrenic disorder) or consciousness disturbance as a complication.
- •Patients who have primary trigeminal neuralgia, diabetic neuropathy, post herpetic neuralgia or acute herpes zoster pain as a complication.
- •Patients who has other serious pain which affect the evaluation of neuropathic pain in cancer.
- •Patients who have sinus bradycardia or serious disturbance of conduction system.
- •Patients who have history of hypersensitivity against hydantoin compound.
- •Patients who are administrated tadalafil (for pulmonary hypertension), rilpivirine, asunaprevir, daclatasvir, vaniprevir, macitentan or sofosbuvir.
- •Patients who are administrated methadone.
- •Patients who have complications such as serious heart disease, hepatic function disorder or renal function disorder which severity are considered by investigator as grade 3 or more severe with reference to ''Concerning classification criteria for seriousness of adverse drug reactions of medical agents'' (except cancer).
- •Patients who received surgical treatment or internal radiation therapy in past three month before the first day of pre observation period.
- •Patients who are treated nerve block, radiation therapy, spinal cord stimulation or surgical treatment for the part of neuropathic pain in past one month before the first day of pre observation period.
- •Patients who change the usage or dosage of medication for cancer as primal disease in the past two week before the first day of the pre observation period, or patients who are predicted not to continue the treatment without change in the medication while this clinical trial.
- •Patients who are administrating with fosphenytoin, phenytoin or ethotoin or have taken these drugs as medication for neuropathic pain.
- •Patients who have participated in other clinical trial and have taken a trial drug in past three month before the first day of pre observation period.
- •Female patients who are pregnant or lactating or who may be pregnancy in the period of the clinical trial.
- •Patients who can not agree to prevent contraception appropriately following the direction of the Investigator or the sub-investigator.
- •Any other patients who are considered by the investigator as unsuitable for participation in the trial.
研究组 & 干预措施
NPC-06 (High dosage)
Active Comparator
18 mg (iv) in Day 1 as an induction dosage and 9 mg (iv) in Day 2 - 7 as a maintenance dosage
干预措施: NPC-06 (Drug)
NPC-06 (Low dosage)
Active Comparator
15 mg (iv) in Day 1 as an induction dosage and 6 mg (iv) in Day 2 - 7 as a maintenance dosage
干预措施: NPC-06 (Drug)
Placebo
Placebo Comparator
Saline will be administered intravenously
干预措施: NPC-06 (Drug)
结局指标
主要结局
Improvement of Numeric Rating Scale (NRS) score within 2 hours after administration
时间窗: Pre-administration, 30, 60, 90 and 120 minutes post-administration
Average change (slope) of NRS score
次要结局
- Other improvements of NRS score(Pre-dose, Days 1,2,3,4,5,6,7,8,9,10,11,12,13)
- Time to event(2 hours after initial administration to Day 7)
- Improvement of Neuropathic Pain Symptom Inventory (NPSI) score(Pre-dose, Days 1,2,3,4,5,6,7,8,9,10,11,12,13)
- Rescue medication use(Day 1 to Day 13)
- Effective concentration(Day 0 to Day 13)
研究者
研究点 (1)
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