EUCTR2010-020402-15-HU进行中（未招募）1 期
Randomised, double-blind, cross-over Phase III study to investigate the efficacy and safety of oxycodone after once daily administration of Oxycodone HCl XL tablets in comparison to twice daily administration of Oxygesic® tablets in patients with chronic cancer pain.
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1.Caucasian male and female patients =18 years of age with chronic cancer pain.
- •2.Patients with predominantly non-neuropathic pain
- •3.Patients requiring continuous oral opioid therapy with at least 40 mg oxycodone per day (or equivalent).
- •4.Adequate analgesia (mean current pain intensity per day =40 mm on VAS) prior to randomisation for at least three consecutive days.
- •5.Stable analgesic requirements prior to randomisation for at least three days (stable maintenance dose of oxycodone; requirement of at least 40 mg oxycodone per day; =2 doses of rescue medication per day), tolerable AEs.
- •6.ECOG (Eastern Cooperative Oncology Group) performance status <3.
- •7.Life expectancy of at least 3 months
- •8.Female patients of childbearing potential agree to undergo pregnancy tests.
- •9.Willingness to undergo a pre-study physical examination and pre- and post-study laboratory investigations.
- •10.Ability to comprehend and willingness to sign informed consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 25
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 25
排除标准
- •1.Hypersensitivity to oxycodone or any of the excipients of the study drugs.
- •2.Patients requiring more than 120 mg oxycodone per day (or equivalent).
- •3.Surgery within 1 month prior to study start and/or anticipated or scheduled surgical intervention during the study.
- •4.Intravenous chemotherapy and/or radiotherapy for pain alleviation and/or neural blockade within 2 weeks prior to study start and/or anticipated and/or scheduled during the course of the study.
- •5.Known or suspected clinically significant respiratory depression, hypoxia, hypercapnia, or decrease in respiratory reserve.
- •6.Known or suspected severe obstructive pulmonary disease, acute or severe bronchial asthma, or cor pulmonale.
- •7.Known or suspected significant hepatic impairment (hepatic transaminases >3 times the upper limit of normal).
- •8.Known or suspected severe renal impairment (CRCL <30 ml/min) or patients with renal failure who are on any form of dialysis.
- •9.Known or suspected significant circulatory disturbance, hypotension, or circulatory shock.
- •10.Known or suspected clinically relevant endocrine disorder, such as myxoedema, not adequately treated hypothyroidism or adrenocortical insufficiency (e.g. Addison's disease)
- •11.Known or suspected paralytic ileus, significant impairment of bowel motility severe enough to potentially result in ileus.
- •12.Known or suspected acute or chronic pancreatitis or biliary tract disease.
- •13.Any gastro-intestinal pathology or surgery or intractable vomiting likely to significantly influence drug absorption.
- •14.Inability to swallow the study drugs whole (e.g. due to dysphagia).
- •15.Known or suspected significant prostatic hypertrophy or urethral stricture severe enough to potentially result in urinary retention.
- •16.Known or suspected CNS depression (signs/symptoms: decreased vital signs, impaired thinking and perception, slurred speech, slowed reflexes, fatigue, decreased consciousness), coma, or convulsive disorder.
- •17.Known or suspected elevation of intracranial pressure.
- •18.Known or suspected acute alcoholism, delirium tremens, or toxic psychosis.
- •19.History of drug addiction or drug seeking behaviour.
- •20.Concomitant treatment with MAO inhibitors.
- •21.Pregnancy or breast-feeding. Women of childbearing potential unable or unwilling to practice adequate contraceptive measures. Reliable methods for women are orally administered hormonal contraceptives, surgical intervention (e.g. tubal ligation), intrauterine device (IUD) and sexual abstinence.
- •22.Any other condition of the patient that in the opinion of the investigator may compromise evaluation of the study treatment or may jeopardize patient’s compliance or adherence to protocol requirements.
- •23.Previous enrolment in this study or participation in any other drug investigational trial within the past 30 days (or five half-lives whichever is longer) prior to enrolment.
- •24.Persons suspected to be at risk of suicide.
- •25.Persons who are not suitable for inclusion in the study in the opinion of the investigator.
研究者
相似试验
进行中（未招募）
不适用
This clinical trial is conducted to investigate whether once daily administration of Oxycodone HCl XL tablets - a new prolonged formulation of oxycodone hydrochloride - is as least effective (or even more effective) and safe as twice daily administration of Oxygesic tablets - a marketed formulation of oxycodone hydrochloride (brand name Oxygesic in Germany) - at the same daily dosage.EUCTR2010-020402-15-DEDevelco Pharma Schweiz AG126
进行中（未招募）
不适用
Randomised, double-blind study to investigate the efficacy and safety of two opioids of which one will be administered once daily and the other twice daily in patients with chronic severe pain.Chronic severe cancer or non-cancer painMedDRA version: 14.1Level: LLTClassification code 10049475Term: Chronic painSystem Organ Class: 10018065 - General disorders and administration site conditionsEUCTR2011-004471-37-SIDevelco Pharma Schweiz AG76
进行中（未招募）
不适用
Randomised, double-blind study to investigate the efficacy and safety of two opioids of which one will be administered once daily and the other twice daily in patients with chronic severe pain.EUCTR2011-004471-37-DEDevelco Pharma Schweiz AG76
进行中（未招募）
不适用
Randomised, double-blind study to investigate the efficacy and safety of two opioids of which one will be administered once daily and the other twice daily in patients with chronic severe pain.Chronic severe cancer or non-cancer painMedDRA version: 14.1Level: LLTClassification code 10049475Term: Chronic painSystem Organ Class: 10018065 - General disorders and administration site conditionsEUCTR2011-004471-37-PLDevelco Pharma Schweiz AG76
已完成
3 期
Randomised double-blind, cross-over Phase III study to investigate the efficacy and safety of oxycodone after once daily administration of Oxycodone HCl XL tablets in comparison to twice daily administration of Oxygesic tablets in patients with chronic paichronic cancer painR52.2Other chronic painDRKS00000577Develco Pharma Schweiz AG89