[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"tourettes-disorder\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:tourettes-disorder":23},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,37,73],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":4,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":25,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":4,"completionDateStruct":4,"leadSponsor":33,"locationsCount":36},"100600134","expanded-access-program-for-treatment-with-ecopipam-for-tourettes-disorder-100600134",false,"NCT07093541","Expanded Access Program for Treatment With Ecopipam for Tourette's Disorder","An Open Label Expanded Access Program Intended to Provide Treatment With Ecopipam (EBS-101) to Children, Adolescents, and Adults in the U.S. With Tourette's Disorder","EBS-101-TD-392","Participants must fulfill all of the following inclusion criteria to be eligible for participation in the Study:\n\n1. Age 6 to 50 years old inclusive at the time of informed consent\u002Fassent.\n2. Participant must sign\u002Fdate the most current Informed Consent Form (ICF). For minor participants the LAR must\u002Fsign date the most current consent and the participant must sign\u002Fdate the most current age-appropriate assent.\n3. In the opinion of the principal investigator (PI), the participant or in the case of a minor their LAR is capable of understanding and complying with protocol and program requirements, oral drug administration and care instructions.\n4. Weight ≥18 kg (39.6 lbs.).\n5. In the opinion of the PI, the participant meets diagnostic criteria for Tourette's Syndrome (TS) per Diagnostic and Statistical manual for Mental Disorders - 5th Edition (DSM-5-TR diagnostic criteria for TD).\n6. The participant must have been treated with an FDA-approved treatment for TD (aripiprazole, haloperidol, or pimozide) or any other D2r antagonist (D2rA) and have experienced treatment failure, tolerability or safety issues as per LAR, participant or prescribing clinician or not have access to any of these approved medications.\n7. Females of child-bearing potential must have a negative urine pregnancy test at Screening.\n8. Females of child-bearing potential who are sexually active or become sexually active must be using double barrier method (condom and IUD, condom and spermicide, etc.) in addition to any oral contraceptive they may be using and agree to continue use of double barrier contraception for the duration of their participation in the study and for 30 days after their last dose of study drug. Females of non-childbearing potential are exempt from this criterion.\n\n   Non-Childbearing potential is defined by:\n   1. Post menopausal defined as \\>= 2 years amenorrheic, or,\n   2. Bilateral salpingo-oopherectomy, or\n   3. Hysterectomy, or\n   4. Pre-menarche\n9. Sexually active male participants must use a barrier method of contraception during the study and agree to continue the use of male contraception for at least 30 days after the last dose of study drug.\n10. Male participants must agree to not donate sperm and female participants not to donate eggs for at least 30 days after the last dose of study drug.\n\nDiagnosis and Main Criteria for Inclusion:\n\nInclusion Criteria\n\nParticipants must fulfill all of the following inclusion criteria to be eligible for participation in the Study:\n\n1. Age 6 to 50 years old inclusive at the time of informed consent\u002Fassent.\n2. Participant must sign\u002Fdate the most current Informed Consent Form (ICF). For minor participants the LAR must\u002Fsign date the most current consent and the participant must sign\u002Fdate the most current age-appropriate assent.\n3. In the opinion of the principal investigator (PI), the participant or in the case of a minor their LAR is capable of understanding and complying with protocol and program requirements, oral drug administration and care instructions.\n4. Weight ≥18 kg (39.6 lbs.).\n5. In the opinion of the PI, the participant meets diagnostic criteria for Tourette's Syndrome (TS) per Diagnostic and Statistical manual for Mental Disorders - 5th Edition (DSM-5-TR diagnostic criteria for TD).\n6. The participant must have been treated with an FDA-approved treatment for TD (aripiprazole, haloperidol, or pimozide) or any other D2r antagonist (D2rA) and have experienced treatment failure, tolerability or safety issues as per LAR, participant or prescribing clinician or not have access to any of these approved medications.\n7. Females of child-bearing potential must have a negative urine pregnancy test at Screening.\n8. Females of child-bearing potential who are sexually active or become sexually active must be using double barrier method (condom and IUD, condom and spermicide, etc.) in addition to any oral contraceptive they may be using and agree to continue use of double barrier contraception for the duration of their participation in the study and for 30 days after their last dose of study drug. Females of non-childbearing potential are exempt from this criterion.\n\n   Non-Childbearing potential is defined by:\n   1. Post menopausal defined as \\>= 2 years amenorrheic, or,\n   2. Bilateral salpingo-oopherectomy, or\n   3. Hysterectomy, or\n   4. Pre-menarche\n9. Sexually active male participants must use a barrier method of contraception during the study and agree to continue the use of male contraception for at least 30 days after the last dose of study drug.\n10. Male participants must agree to not donate sperm and female participants not to donate eggs for at least 30 days after the last dose of study drug.\n\nParticipants cannot be enrolled in the study if they meet any of the following criteria.\n\n1. Clinically meaningful abnormalities on laboratory tests at Screening as determined by the PI.\n2. Specific laboratory findings at enrollment\n\n   1. T. Bili \\>= 2.5 x ULN for age (Participants with a history of Gilbert's Disorder must have prior documentation of the disorder.)\n   2. ALT \\>= 2.5 x ULN for age\n   3. AST \\>= 2.5 x ULN for age\n   4. Positive urine drug screen for cocaine, amphetamine, benzodiazepines, barbiturates, phencyclidine (PCP), or opiates at Screening, except those receiving stable, prescribed treatment for attention deficit\u002Fhyperactivity disorder (ADHD) or a positive for benzodiazepine prescribed (either routine or as needed) for any anxiety disorder or anxiety associated with a depressive disorder\n   5. Severe renal impairment or end stage renal disease as defined by eGFR \\\u003C 60 ml\u002Fmin\u002F1.73m2\n3. Any of the following cardiovascular:\n\n   1. ECG with a QTcF \\> 450 for males or \\> 470 for females at screening.\n   2. A history or finding on the screening ECG of any significant arrhythmia in the opinion of the principal investigator\n   3. A known family history of QT prolongation syndrome with sudden death\n   4. Current or anticipated need for medications known to prolong the QT interval\n4. A lifetime history of any of the following disorders:\n\n   1. Myocardial Infarction\n   2. Cancer (excluding Basal Cell Carcinoma or Cervical Cancer in situ)\n   3. Seizure Disorder (except febrile seizure)\n   4. Neuroleptic Malignant Syndrome\n   5. Tardive Dyskinesia\n   6. Parkinson's Disorder\n   7. Dementia\n   8. Essential Tremor\n   9. Substance Use Disorders (as defined by DSM-5-TR) in the past 6 months prior to screening. (Excluding nicotine and\u002For caffeine)\n   10. Any general medical disorders OR psychiatric disorder that are not under good control in the opinion of the PI OR require treatment with any prohibited medication.\n5. All prescription or over-the-counter drug (e.g., St. Johns Wort) that are strong and moderate inhibitors or inducers of CYP3A4; drugs that are substrates of CYP2D6; or drugs that are substrates of MATE-2K transporters (e.g., metformin).\n6. At significant risk of attempting suicide in the opinion of the PI or any one of the following:\n\n   1. A history of a suicide attempt OR behavior in the past one year prior to Screening.\n   2. A lifetime history of 2 or more suicide attempts OR behaviors.\n   3. A history of non-suicidal self-injurious behavior in the past 2 years prior to Screening.\n   4. A history of suicide ideation OR thoughts in the past 6 months prior to Screening.\n7. Female participants who are currently pregnant or lactating or planning to become pregnant during the study.\n8. A history of hypersensitivity or allergic reaction to ecopipam or any inactive ingredient of the formulation.\n9. Participants unable to swallow tablets.\n10. Any participant who in the opinion of the PI or the Sponsor is not a suitable candidate for the program.","ALL","6 Years","50 Years","EXPANDED_ACCESS","The goal of this expanded access study is to learn about the long-term effects of Ecopipam in participants with Tourette's Disorder (TD). The main question it aims to answer is:\n\n* Is ecopipam safe and well-tolerated in participants equal and over the age of 6 to 50 with TD?\n* Assess quality of life measures and to provide access to ecopipam while NDA is being prepared and submitted for review for marketing approval\n\nEligible participants with TD will take ecopipam with guidance from their treating physician. In addition to the standard of care from the treating physician, treatment with ecopipam will continue until ecopipam becomes commercially available in the United States or the program is terminated.\n\nWhile in the EAP program, participants will be asked regarding how safe and tolerable ecopipam is to the participant. Several questionnaires will be collected regarding participants experiences while taking ecopipam during monthly visits for the first year and every three months thereafter until the conclusion of the study.",[23,24],"Tourettes Disorder","Tourette Disorder",[26,27],"Tourettes Syndrome","Ecopipam Tourette Disorder","AVAILABLE","2026-05-14",{"date":31,"type":32},"2026-05-18","ACTUAL",{"name":34,"class":35},"Emalex Biosciences Inc.","INDUSTRY",26,{"id":38,"slug":39,"hasResults":11,"nctId":40,"briefTitle":41,"officialTitle":41,"acronym":42,"eligibilityCriteria":43,"healthyVolunteers":11,"sex":17,"minAge":44,"maxAge":4,"enrollmentInfo":45,"targetDuration":4,"studyType":48,"phases":49,"briefSummary":51,"conditions":52,"keywords":4,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":72},"100547491","remote-delivery-of-a-mindfulness-based-intervention-for-tics-100547491","NCT06408662","Remote Delivery of a Mindfulness-based Intervention for Tics","MBIT","Inclusion Criteria:\n\n1. be ≥18 years of age;\n2. meet diagnostic criteria for a primary or co-primary diagnosis of Tourette Syndrome or a Persistent Motor or Vocal Tic Disorder on a structured clinical interview;\n3. have moderate or greater tic severity as evidenced by a YGTSS Total Tic Score of \\>14 (when motor and vocal tics are present) or \\>10 (when only motor or vocal tics are present);\n4. be medication free and\u002For on a stable dose of psychiatric medication 8 weeks prior to study participation;\n5. be not engaged in psychotherapy for non-TS conditions and\u002For be on a stable course of therapy for 6 months prior to study participation\n6. be fluent in English;\n7. have access to a smart phone and\u002For tablet.\n\nExclusion Criteria:\n\n1. a current diagnosis of substance use disorder, psychosis, mania or another condition that requires another form of care;\n2. severe current suicidal\u002Fhomicidal ideation and\u002For self-injury requiring medical intervention;\n3. concurrent psychotherapy for TS;\n4. prior extensive experience with mindfulness and\u002For meditation.","18 Years",{"count":46,"type":47},150,"ESTIMATED","INTERVENTIONAL",[50],"NA","This research study is being done to compare a mindfulness-based intervention for tics (MBIT) to psychoeducation with relaxation and supportive therapy (PRST) for individuals with Tourette's syndrome or Persistent Tic Disorders (collectively TS). It is the investigator's hope that this information cam be used to improve current treatments for individuals with TS.",[53,54,55,56,57,58,59,60],"Tourette Syndrome","Tourette's Disorder","Chronic Motor Tic Disorder","Chronic Vocal Tic Disorder","Persistent Motor Tic Disorder","Persistent Vocal Tic Disorder","Persistent Tic Disorder","Tic Disorders","RECRUITING","2026-05-07",{"date":64,"type":32},"2026-05-11",{"date":66,"type":32},"2024-05-23",{"date":68,"type":47},"2028-12",{"name":70,"class":71},"Johns Hopkins University","OTHER",1,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":17,"minAge":44,"maxAge":19,"enrollmentInfo":80,"targetDuration":4,"studyType":48,"phases":82,"briefSummary":83,"conditions":84,"keywords":86,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":72},"100477651","forehead-temperature-regulating-therapy-for-insomnia-in-adults-with-tourettes-disorder-100477651","NCT05499741","Forehead Temperature-Regulating Therapy for Insomnia in Adults With Tourette's Disorder","Piloting Forehead Temperature-Regulating Therapy for Insomnia in Adults With Tourette's Disorder","Inclusion Criteria:\n\n* DSM-5 diagnosis of Tourette's disorder\n* DSM-5 diagnosis of Insomnia disorder\n* Yale Global Tic Severity Scale Score ≥ 14 for Tourette's disorder or ≥ 10 for persistent motor tic disorder or persistent vocal tic disorder\n* Insomnia Severity Index score \\> 14\n* Sleep efficiency ≤ 85 per cent on 50 percent or greater nights over monitoring week, per Consensus Sleep Diary\n* Age of 18 to 50 years\n* English fluency\n\nExclusion Criteria:\n\n* Current or lifetime diagnosis of bipolar disorder, psychosis, or pervasive developmental disorder\n* Suicidality, severe depression or anxiety, or alcohol or substance dependence present within the past 6 months\n* Moderate to severe sleep apnea risk per score of ≥ 3 on the Stop-Bang Questionnaire\n* current diagnosis of Narcolepsy\n* Wechsler Abbreviated Scale for Intelligence-Second Edition IQ score \\\u003C 80\n* Changes in prescribed or over-the-counter medications for sleep within prior month and planned during the study\n* Changes in tic or other psychotropic medication within prior month and planned during study\n* Caffeine use \\> 3 cups per day\n* Behavior therapy for tics or sleep within prior 3 months\n* Travel across \\> 2 time zones in prior month\n* Shift work, or irregular sleep schedule (i.e., nightly variation of \\> 3 hours in bedtime or wake time, or time in bed duration \\\u003C 5.5 or \\> 10 hours per night)\n* Raynaud's disease or severe cold sensitivity\n* Other major medical or neurological condition",{"count":81,"type":47},25,[50],"The primary aim of the present research project is to investigate the preliminary effects of four weeks of forehead temperature-regulating therapy on insomnia in adults with Tourette's disorder and co-occurring insomnia disorder. This project will also examine the effects of the device on depression, anxiety, and daytime sleepiness, and explore its effects on tic severity.",[54,85],"Insomnia",[87,88,89,90,91],"tics","insomnia","sleep","temperature","device","2025-03-13",{"date":94,"type":32},"2025-03-17",{"date":96,"type":32},"2023-04-27",{"date":98,"type":47},"2026-01",{"name":100,"class":71},"University of California, Los Angeles"]