跳至主要内容
临床试验/EUCTR2015-001549-96-BG
EUCTR2015-001549-96-BG进行中(未招募)1 期

A MULTICENTER, OPEN-LABEL, FOLLOW-UP STUDY TO ASSESS THE LONG-TERM USE OF LACOSAMIDE (FLEXIBLE DOSE FROM 200 TO 600 MG/DAY) USED AS MONOTHERAPY IN SUBJECTS WHO COMPLETED SP0994 AND RECEIVED LACOSAMIDE MONOTHERAPY TREATMENT

CB BioPharma SPR0 个研究点目标入组 150 人开始时间: 2015年11月3日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
150

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. An Institutional Review Board (IRB)/Independent Ethics Committee (IEC) approved written Informed Consent form is signed and dated by the subject or by the parent(s) or legal representative.
  • •2. Subject/legal representative is considered reliable and capable of adhering to the protocol, visit schedule, and medication intake according to the judgment of the investigator.
  • •3. Subject has completed the Termination Visit of SP0994 and has been treated with Lacosamide monotherapy.
  • •Are the trial subjects under 18? yes
  • •Number of subjects for this age range: 1
  • •F.1.2 Adults (18-64 years) yes
  • •F.1.2.1 Number of subjects for this age range 134
  • •F.1.3 Elderly (>=65 years) yes
  • •F.1.3.1 Number of subjects for this age range 15

排除标准

  • •1. Subject is receiving any investigational drugs or using any experimental devices in addition to Lacosamide.
  • •2. Subject experienced a seizure at the third target dose (ie, Lacosamide 600 mg/day) during SP0994.
  • •3. Subject requires another antiepileptic drug for the treatment of seizures.
  • •4. Subject meets a must” withdrawal criterion for the previous study, SP0994.
  • •5. Subject is experiencing an ongoing serious adverse event from the previous study, SP0994.
  • •6. Female subject who is pregnant or nursing, and/or a woman of childbearing potential who is not surgically sterile, 2 year postmenopausal or does not practice one highly effective method of contraception (according to ICH guidance defined as those that result in a failure rate of less than 1% per year when used consistently and correctly), unless sexually abstinent, for the duration of the study.

研究者

发起方
CB BioPharma SPR

相似试验

进行中(未招募)
1 期
A clinical study to investigate the long-term use of Lacosamide as monotherapy in subjects who completed SP0994.Epilepsy with partial-onset seizures or generalized tonic-clonic seizuresMedDRA version: 18.1 Level: PT Classification code 10015037 Term: Epilepsy System Organ Class: 10029205 - Nervous system disorders
EUCTR2015-001549-96-FRCB BioPharma SPR150
进行中(未招募)
1 期
A clinical study to investigate the long-term use of Lacosamide as monotherapy in subjects who completed SP0994.Epilepsy with partial-onset seizures or generalized tonic-clonic seizuresMedDRA version: 18.1Level: PTClassification code 10015037Term: EpilepsySystem Organ Class: 10029205 - Nervous system disorders
EUCTR2015-001549-96-PLCB BioPharma SPR150
进行中(未招募)
1 期
A clinical study to investigate the long-term use of Lacosamide as monotherapy in subjects who completed SP0994.Epilepsy with partial-onset seizures or generalized tonic-clonic seizuresMedDRA version: 18.0 Level: PT Classification code 10015037 Term: Epilepsy System Organ Class: 10029205 - Nervous system disorders
EUCTR2015-001549-96-LVCB BioPharma SPR150
进行中(未招募)
1 期
A clinical study to investigate the long-term use of Lacosamide as monotherapy in subjects who completed SP0994.Epilepsy with partial-onset seizures or generalized tonic-clonic seizuresMedDRA version: 20.0 Level: PT Classification code 10015037 Term: Epilepsy System Organ Class: 10029205 - Nervous system disorders
EUCTR2015-001549-96-FICB BioPharma SPR150
进行中(未招募)
1 期
A clinical study to investigate the long-term use of Lacosamide as monotherapy in subjects who completed SP0994.Epilepsy with partial-onset seizures or generalized tonic-clonic seizuresMedDRA version: 20.0 Level: PT Classification code 10015037 Term: Epilepsy System Organ Class: 10029205 - Nervous system disorders
EUCTR2015-001549-96-SECB BioPharma SPR150