Asitri Dashboard Search Clinical Trials
The U.S. National Library of Medicine provides a database of clinical trials worldwide. Use the fields below to search the database. Expand your results and select terms or phrases and right-click to search using Google, MalaCards, MedlinePlus, PubMed, or Wikipedia.
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Clinical Trials Search Results
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Count: 80
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| NCT ID | Title | ||
|---|---|---|---|
| NCT06259331 | Evaluation of Viloxazine and Its Metabolite 5-Hydroxy-viloxazine Glucuronide Into Breast Milk in Healthy Lactating Women | ||
| NCT02614547 | A Study to Evaluate SAGE-547 in Participants With Severe Postpartum Depression | ||
| NCT03247530 | Evaluation of SPN-812 (Viloxazine Extended-release Capsule) Low Dose in Children With ADHD | ||
| NCT03638466 | Exploratory fMRI Study on the Treatment for Impulsive Aggression in Children With ADHD | ||
| NCT01246765 | National Pregnancy Registry for Psychiatric Medications | ||
| NCT00626236 | Phase 2a Study of Safety and Tolerability of SPN-810 in Children With ADHD and Persistent Serious Conduct Problems | ||
| NCT06185985 | Open-label Safety and Efficacy of SPN-812 (Viloxazine Extended-release Capsule) in Adults With ADHD and Mood Symptoms | ||
| NCT05518578 | Safety and Tolerability Study of SPN-817 in Adult Patients With Treatment Resistant Epilepsy | ||
| NCT04602624 | A Study to Evaluate the Safety and Tolerability of SAGE-718 in Participants With Mild Cognitive Impairment or Mild Dementia Due to Alzheimer's Disease (AD) | ||
| NCT05645432 | An Open-Label Study Evaluating Brexanolone in Adults With Tinnitus | ||
| NCT02433314 | An Open Label, Expanded Access Protocol With SAGE-547 for Super-Refractory Status Epilepticus | ||
| NCT04143217 | Open-label Long-Term Safety and Efficacy of SPN-812 (Viloxazine Extended-release Capsule) in Adults With ADHD | ||
| NCT05318937 | A Study to Evaluate the Effects of SAGE-718 in Participants With Parkinson's Disease Cognitive Impairment | ||
| NCT03844906 | A Study to Assess Electrophysiology, Safety, Tolerability, and Pharmacokinetics of Multiple Doses of SAGE-718 Using Ketamine Challenge in Healthy Subjects | ||
| NCT04099667 | Efficacy and Safety Study of MYOBLOC® in the Treatment of Adult Lower Limb Spasticity | ||
| NCT02736656 | Open-label Study to Evaluate Long-term Safety and Efficacy of SPN-812 (Viloxazine Extended-release Capsule) | ||
| NCT02942017 | A Study to Evaluate Safety and Efficacy of SAGE-547 in Participants With Moderate Postpartum Depression (547-PPD-202C) | ||
| NCT03924492 | Expanded Access Protocol of ZULRESSO™ (Brexanolone) Injection for Adult Patients With Postpartum Depression | ||
| NCT03787758 | A Study to Evaluate Safety, Tolerability, and Pharmacokinetics of SAGE-718 Oral Solution in Patients With Huntington's Disease - Part B | ||
| NCT05358821 | 28-Day Study of SAGE-718 on Functioning Capacity in Participants With Huntington's Disease | ||
| NCT01085461 | Assessment of Suicidality in Epilepsy - Rating Tools | ||
| NCT03156439 | Bioavailability, Safety, and Tolerability of BIS-001 ER | ||
| NCT05097079 | Efficacy and Safety Study of MYOBLOC in the Treatment of Sialorrhea in Pediatric Subjects | ||
| NCT07141329 | SPN-817 Open-Label Extension Study in Adults With Focal Onset Seizures | ||
| NCT02618434 | Treatment of Impulsive Aggression in Subjects With ADHD in Conjunction With Standard ADHD Treatment (CHIME 2) | ||
| NCT05102552 | Evaluating the Safety and Relative Bioavailability of Three SPN-817 Treatments (A, B and C) in Healthy Adult Subjects | ||
| NCT03665038 | A Study to Assess the Safety of Brexanolone in the Treatment of Adolescent Female Participants With Postpartum Depression (PPD) | ||
| NCT05059600 | A Study To Assess The Safe-Use Conditions For Administration of ZULRESSO® in a Home Setting | ||
| NCT05619692 | A Study to Evaluate the Effects of SAGE-718 in Participants With Mild Cognitive Impairment or Mild Dementia Due to Alzheimer's Disease (AD) | ||
| NCT01416064 | Open-Label, Extension Study to 810P202 | ||
| NCT00515437 | A Multi-Center Study of MYOBLOC for the Treatment of Sialorrhea in Parkinson's Disease Patients | ||
| NCT05066672 | Phase 2 Study of NV-5138 in Adults With Treatment Resistant Depression | ||
| NCT01994109 | Efficacy and Safety Study of MYOBLOC® in the Treatment of Sialorrhea in Adult Subjects | ||
| NCT00918424 | Long Term Study of the Safety of OXC XR as in Pediatric Epilepsy Subjects | ||
| NCT03944785 | Clinical Outcome Assessment of Parkinson's Disease Patients Treated With XADAGO (Safinamide) | ||
| NCT01770145 | Apokyn for Motor IMProvement of Morning AKinesia Trial (AM IMPAKT) | ||
| NCT03615703 | Functional MRI Study in Healthy Children Engaged in Aggressive Behaviors | ||
| NCT04815967 | Efficacy and Safety Study of MYOBLOC® in the Treatment of Adult Upper Limb Spasticity | ||
| NCT01107496 | Evaluation of Immediate-Release Viloxazine in Adults With ADHD | ||
| NCT05107128 | A Study to Evaluate the Effect of SAGE-718 on Cognitive Function in Participants With Huntington's Disease (HD) | ||
| NCT02052739 | Study to Evaluate SAGE-547 Injection as Adjunctive Therapy for the Treatment of Super-Refractory Status Epilepticus | ||
| NCT03770780 | A Study to Assess the Electrophysiology, Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Response Using Magnetic Resonance Imaging of SAGE-718 Using a Ketamine Challenge in Healthy Subjects | ||
| NCT02023606 | Phase I Study to Assess the Absorption, Metabolism, and Excretion of [14C] Labeled SPN-810M | ||
| NCT02942004 | A Study to Evaluate Efficacy and Safety of SAGE-547 in Participants With Severe Postpartum Depression (547-PPD-202B) | ||
| NCT01284530 | Evaluation of the Pharmacokinetics, Safety, and Tolerability of TPM XR as Adjunctive Therapy in Pediatric Subjects With Epilepsy | ||
| NCT03247517 | Evaluation of SPN-812 (Viloxazine Extended-release Capsule) Low Dose in Adolescents With ADHD | ||
| NCT02477618 | A Study With SAGE-547 for Super-Refractory Status Epilepticus | ||
| NCT03247543 | Evaluation of SPN-812 (Viloxazine Extended-release Capsule) High Dose in Children With ADHD | ||
| NCT00908349 | Safety and Tolerability of OXC XR as Adjunctive Therapy in Subjects With Refractory Partial Epilepsy | ||
| NCT02285504 | Evaluate SAGE-547 in Female Participants With Severe Postpartum Depression |
