Myasthenia Gravis
- A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel, Multicenter Study to
Evaluate the Safety and Efficacy of ALXN1720 in Adults with Generalized Myasthenia Gravis - DNTH103‑MG‑201: A Phase 2, Randomized, Blinded, Placebo-Controlled, Study to Evaluate Safety,
Tolerability, Pharmacometrics, and Efficacy of DNTH103 in Adults with Generalized Myasthenia Gravis (MAGIC) - Phase 3 Study to Assess Efficacy and Safety of Batoclimab as Induction and Maintenance Therapy in Adult Participants with gMG
- A Phase 2b, Multicenter, Randomized, Placebo-Controlled, Double-Blind Study to Assess the Efficacy and Safety of IMVT-1402 in Patients With Mild to Severe Myasthenia Gravis
- A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study with an Open-label Extension Period to Evaluate the Efficacy and Safety of Telitacicept in Patients with Generalized Myasthenia Gravis
- A randomized, double-blind, placebo-controlled phase III study to evaluate the efficacy, safety, and tolerability of remibrutinib in patients with generalized Myasthenia Gravis, followed by an open-label extension phase
- MS700568_0183 (MyClad), A Phase 3, Randomized, Double-Blind, Placebo-Controlled, 3-Arm, 3-Period Study to assess the Efficacy and Safety of a New Formulation of Oral Cladribine compared with Placebo in Participants with Generalized Myasthenia Gravis
- A Phase 1b/2a Double Blind, Randomized, Placebo Controlled Study to Evaluate the Safety, Tolerability, Pharmacodynamics, and Efficacy of CNP-106 in Subjects Ages 18–75 with Generalized Myasthenia Gravis
- Long-Term, Observational, Global Registry of Patients With Generalized Myasthenia Gravis Who Have Received Treatment With Complement C5 Inhibition Therapies
Chronic Inflammatory Demyelinating Polyneuropathy
- A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of DNTH103 in Adults with Chronic Inflammatory Demyelinating Polyneuropathy (CAPTIVATE)
- A Phase 3, Double-blind, Placebo-controlled Study Evaluating Efficacy and Safety of Riliprubart in Participants with Refractory Chronic Inflammatory Demyelinating Polyneuropathy
- A Phase 3, Randomized, Double-blind, Study Evaluating Efficacy and Safety of Riliprubart versus Intravenous Immunoglobulin (IVIg) in
Participants with Chronic Inflammatory Demyelinating Polyneuropathy
Migraine
- Pediatric Options for Migraine Relief: A randomized, double-blind, placebo-controlled study of
lasmiditan for acute treatment of migraine: PIONEER-PEDS1 Study. - A Phase 3, 12-Month, Open-Label Study of Lasmiditan in Pediatric Patients
with Migraine – PIONEER-PEDS2 - Interventional, randomized, double-blind, parallel-group, placebo-controlled study to evaluate the efficacy and safety of IV eptinezumab in adolescents (12-17 years) for the preventive treatment of chronic migraine
- Long-term, open-label (dose-blinded), extension study of eptinezumab in children and adolescents with chronic or episodic migraine
Thyroid Eye Disease
- A randomized, double-masked, placebo-controlled safety, tolerability, and efficacy study of VRDN-001, a humanized monoclonal antibody
directed against the IGF-1 receptor, in participants with chronic thyroid eye disease (TED) - An open-label study for participants who are non-responders at the end of treatment assessment on the VRDN-001-101 and VRDN-001-301 pivotal studies
- A Multicenter Phase 2b Randomized, Double-Masked, Placebo-Controlled Dose-Ranging Study of TOUR006 in Participants with Thyroid Eye Disease
Epilepsy
- A Randomized, Double-blind, Placebo-Controlled, Multicenter Phase 3 Study to
Evaluate the Safety, Tolerability, and Efficacy of XEN1101 as Adjunctive Therapy in Focal-Onset
Seizures - A Randomized, Double-blind, Placebo-Controlled, Multicenter, Phase 3 Study to Evaluate the Safety, Tolerability, and Efficacy of XEN1101 as Adjunctive Therapy in Primary Generalized Tonic-Clonic Seizures
- A Multicenter, Open-label, Long-term, Safety, Tolerability, and Efficacy Study of
XEN1101 in Subjects Diagnosed With Epilepsy
Stroke
- A Phase 3, Randomized, Double-Blind, Parallel Group, Placebo-Controlled Study to Demonstrate the Efficacy and Safety of an Oral Factor XIa Inhibitor, after an Ischemic Stroke or High Risk Transient Ischemic Attack
- Phase 3 study to investigate the efficacy and safety of the oral FXIa inhibitor Asundexian (BAY 2433334) compared with placebo in participants after an acute noncardioembolic ischemic stroke or high-risk TIA (OCEANICStroke)
Parkinson’s Disease
- A Phase 2, Randomized, Double-blind, Sham Surgery-controlled Study of the Efficacy and Safety of Intraputaminal AAV2-GDNF in the Treatment of Adults with Moderate Stage Parkinson’s Disease
- 58-Week Open-label Trial of Tavapadon in Parkinson’s Disease (TEMPO-4 Trial)
- A Randomized Placebo-controlled Trial of Zoledronic Acid for Prevention of Fractures in Patients with Parkinson’s Disease
Cervical Dystonia
- A Phase 2a, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Safety, Tolerability and Efficacy of MTR-601, a Novel Oral Treatment in Patients with Cervical Dystonia.
Alzheimer’s Disease
- Visualizing Brain Proteinopathies Using [F-18]Flornaptitril-PET in the Prediction of Clinical Progression of Mild Cognitive Impairment with Either Suspected Chronic Traumatic Encephalopathy or Alzheimer’s Disease
If interested in study participation, please contact:
Aubrey Alexander, CCRC
Clinical Research Manager
Department of Neurology
Phone: 517-884-8920
Email: alexaub@msu.edu