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An Exploratory Study of the Potential for Rational Immune System Manipulation to Prevent Emergence of Synucleinopathy Manifestations in Persons With REM Sleep Behavior Disorder (RBD)

NCT06996652 · Yale University
In plain English

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About this study
Primary Objective: To assess the ability of adalimumab as compared to placebo to reduce or prevent progression of synuclein-related neurodegeneration in persons with idiopathic REM Sleep Behavior Disorder (RBD). Secondary Objective, Safety: Safety will be assessed by monitoring the incidence of adverse events, clinical laboratory abnormalities, serious infections, signs and symptoms suggestive of new onset demyelinating disease, incidence of new demyelinating lesions on brain MRI scan and number of study participants who develop serum anti-adalimumab antibodies (ADAs). Secondary Objective, Clinical: To assess the effect of adalimumab treatment on change in clinical measures presumptively related to underlying neurodegeneration. The key secondary endpoint of interest will be a composite outcome. A study participant will be considered to have met the study endpoint upon the attainment of at least 1 of the following milestones at 2 consecutive study visits at least 3 months apart: * Increase from baseline of \> 2 points on the combined MDS-UPDRS Parts 1b and 2, OR * Increase from baseline in MDS-UPDRS Part III motor score \> 4 points, OR * Decrease from baseline in MoCA of \> 3 points, OR * Participant is diagnosed with PD, DLB, or MSA by a Movement Disorder specialist or a neurologist specializing in cognitive disorders, OR * Participant has initiated pharmacologic treatment for PD-, DLB-, or MSA-related symptoms Additional (or Exploratory) Objectives: * To evaluate the pharmacodynamic effect of adalimumab on biomarkers of immune system dysfunction in RBD patients to predict response to treatment * To evaluate the effect of adalimumab on selected biomarkers reflective of neurodegeneration * To evaluate effects of adalimumab treatment on selected measures of quality of life After a 12-week screening period, subjects will be randomized 1:1 to receive active or placebo treatment. Thereafter, subjects will be seen in clinic at 4, 12 and 24 weeks after their initial dose, and then at approximately 24-week intervals up to Week 96. A safety follow-up visit will occur 70 days after the last dose of study treatment. At specified visits, safety and clinical and biomarker assessments will be obtained, and study medication will be dispensed. Quantitative motor and cognitive assessments will be completed at home at intervals between in-person study visits. At 6-month intervals, subjects will be given a body-worn sensor that they will wear for 7 days to record patterns of activity during sleep and wakefulness. Subjects who meet one of the clinical secondary endpoints will remain in the study until its termination. Approximately 25 subjects in each treatment group will be enrolled in an Cerebrospinal Fluid (CSF) biomarker sub-study. Subjects in this sub-study: Individuals participating in the CSF sub-study will undergo lumbar punctures at baseline and at yearly intervals, thereafter, to assess the effects of adalimumab on biomarkers of immune processes and neurodegeneration in the CSF.
Eligibility criteria
Inclusion Criteria: * Males, or females who are either 1. post-menopausal or otherwise not of child-bearing potential, defined as either 1) having had no menses for 12 or months without an alternative medical cause or explanation or 2) having undergone a surgical procedure (hysterectomy, bilateral tubal ligation) that prevents conception, or 2. practicing adequate contraception. Female participants of childbearing potential must practice at least 1 protocol-specified method of birth control, that is effective from 30 days before baseline (or earlier) through at least 150 days after the last dose of the study drug. Female participants of non-childbearing potential do not need to use birth control. 3. women of childbearing potential must have a negative urine pregnancy test prior to enrollment, and agree to undergo a pregnancy test at each study visit. Women with a positive pregnancy test at screening or at any subsequent study visit will be withdrawn from the study. * Diagnosis of idiopathic REM Sleep Behavior Disorder (RBD) based upon: 1. History of Dream Enactment Behavior during sleep and 2. Evidence of REM sleep without muscle atonia based upon polysomnogram obtained in a qualified sleep laboratory, consistent with ICSD-3 Diagnostic Criteria for RBD * Hyposmia, defined as score \< 15th percentile for age-and gender-specific normal values * Not diagnosed with motor Parkinson's Disease or Lewy Body Dementia * Have a MoCA score at screening and baseline ≥23 * Able to speak, read and write fluently in the official language of the site's geographical region * Participant must be willing and able to attend all study visits as required by the study protocol * Participant must have a study partner who is in regular contact with the subject and can accompany the subject to clinic visits and report on subject's functional status * Participant must be able to self-inject study drug regularly or have a study partner who is available, willing and able to do so * Participant must be able to understand the study requirements and provide written informed consent Exclusion Criteria: * Women who are pregnant, planning to become pregnant, or currently breastfeeding * Alternative explanation or etiology for the presence of RBD (e.g. narcolepsy) * Other than RBD, neurologic or medical disorder which may impair cognition including: head trauma, seizure disorder, neurodegenerative disease, hydrocephalus, cerebral/spinal hematoma, inflammatory disease, CNS infection (e.g., encephalitis or meningitis), neoplasm, toxic exposure, metabolic disorder (including hypoxic or hypoglycemic episodes), or endocrine disorder, or any significant medical conditions that, in the opinion of the investigator, would prohibit their participation in the study. * As assessed by the central reader, MRI evidence of (a) more than three lacunar infarcts, (b) territorial infarct or macroscopic hemorrhage, or (c) deep white matter lesions corresponding to a Fazekas score of 3 * Any contra-indication to undergo MRI, as judged by local PI or radiologist, including but not limited to presence of pacemaker, aneurysm clips, artificial heart valves, ear implants, ventriculoperitoneal shunt, foreign metal objects in the eyes, skin or body or any other circumstance which would contra-indicate an MRI scan or impair MRI image quality, or history of claustrophobia or of not tolerating MRI scanning procedures * History or active presence of any of the following neurological, psychiatric or medical conditions: 1. Large vessel stroke 2. Peripheral or CNS demyelinating disease 3. Chronic and/or recurrent fungal, bacterial or opportunistic infections 4. Myocardial infarction or unstable angina within the previous 12 months 5. Clinically relevant or significant ECG abnormalities, including ECG with QT interval corrected for heart rate using Fridericia's formula (QT interval corrected for heart rate using Fridericia's formula) \> 450 msec (males) or \> 470 msec (females). 6. Congestive heart failure, NYHA Class 3 or 4 7. Autoimmune disease (e.g., Systemic Lupus Erythematosis (SLE), or symptoms suggestive of a lupus-like syndrome, multiple sclerosis, rheumatoid arthritis, Type 1 diabetes mellitus, inflammatory bowel disease, psoriasis, etc.) 8. Immunocompromised systemically due to continuing effects of immune suppressing medication 9. Current or previous hepatitis B infection (defined as positive test for hepatitis B surface antigen (HbSAg) and/or hepatitis B core antibody (anti-HBc). * Participants with immunity to hepatitis B (if due to natural infection defined as negative HBsAg, positive hepatitis B antibody (anti-HBs) and positive anti-HBc; if due to vaccination defined as negative HBsAg, negative anti-HBc and positive anti-HBs are eligible to participate in the study * For patients with resolved HBV infection, if anti-HBc negative, HBV DNA testing is needed prior to initiating study drug j. History or positive test at Screening for hepatitis C virus antibody (anti-HCV) in the absence of treatment resulting in cure k. History or positive test at Screening for human immunodeficiency virus (HIV) l. History of untreated or incompletely treated tuberculosis or a positive tuberculosis IGRA test. m. History of malignancy other than successfully treated, non-metastatic cutaneous squamous or basal cell carcinoma or localized carcinoma in situ of the cervix n. Major depressive episode requiring initiation of medication or hospitalization within the previous 90 days o. Seated blood pressure \> 150/90 on 3 separate determinations p. Presence of hallucinations or delusions q. Psychiatric disorder (schizophrenia, schizoaffective disorder, etc.) associated with psychosis r. Active infection(s) requiring treatment with intravenous anti-infectives within 30 days, or oral/intramuscular anti-infectives within 14 days prior to baseline s. Major surgery within 12 weeks of screening t. Blood donation of 1 unit or more within 8 weeks prior to the first dose of study medication * Any of the following laboratory abnormalities at Screening 1. Screening values for hemoglobin \< 12 g/d for men or \< 11 g/dL for women or other clinically significant hematological abnormality 2. Any serum chemistry value (e.g., AST, ALT, alkaline phosphatase, CK, total bilirubin etc. \> 2x the upper limit of normal on 2 successive determinations less than 2 weeks apart 3. Serum creatinine above the ULN or eGFR \< 60 mL/min/1.73 m2 4. Platelet count, INR, PT or PTT not within the normal range or other risk for increased or uncontrolled bleeding * Any other significant medical conditions that, in the opinion of the investigator, would prohibit participation in the study, including inability to tolerate the MRI scan * For participants agreeing to lumbar puncture: Presence of contra-indication to lumbar puncture as judged by local PI (e.g., known X-ray or other evidence of significant lumbar spine abnormalities or history of lumbar surgery with sequalae that would interfere with or pose risks from the procedure; platelet count below 50,000 cells/mL; need for anticoagulant or antiplatelet medications other than aspirin at a dose of \< 100 mg/day or clopidogrel (see item 10 (g) below)) * Taking any of the following medications: 1. Symptomatic anti-Parkinson agents, including but not limited to levodopa-containing preparations, dopamine agonists, monoamine oxidase inhibitors, amantadine, and adenosine receptor antagonists taken any time prior to the screening visit 2. Cognitive enhancing agents, including but not limited to acetylcholinesterase inhibitors and memantine taken any time prior to the screening visit 3. Stimulant medications, including but not limited to lisdexamphetamine, dextroamphetamine/amphetamine (Adderall) and methylphenidate taken at any time prior to the screening visit 4. Antipsychotic agents, including pimavanserin 5. Antidepressant medications whose dose has not been stable for at least 90 days 6. Use of any of the following medications within 12 months prior to Screening: Immunosuppressant medications, including chronic corticosteroids, anakinra and abatacept 7. Any previous use of injected or infused antibody therapies, including but not limited antibodies directed against TNF, anti-IL-6, natalizumab, rituximab, conventional or targeted DMARD agents 8. For participants agreeing to undergo lumbar puncture: Anticoagulant or anti-platelet medications including warfarin, heparinoids and direct coagulation factor inhibitors (e.g., apixaban, dabigatran, rivaroxaban) within 90 days of the planned first dose of study drug; either aspirin at a dose of \<¬ 100 mg/day or clopidogrel at a dose of 75 mg/day, but use of both in combination is permitted. 9. Received any live vaccine, with the exception of non-replicating live viral vaccines such as Jynneos vaccine, within 30 days prior to the first dose of study drug, or expected need of live vaccination during study participation including at least 70 days after the last dose of study drug. * History of an allergic reaction or significant sensitivity to adalimumab or constituents of the study drug (and its excipients) and/or other products in the same class * Participation in any other interventional clinical trial, or treatment with any investigational drug or investigational use of an approved therapy within 30 days (or 5 half-lives of such agent) prior to the first Screening visit. * History of drug or alcohol abuse within the last 5 years (including cannabis use disorder) * Positive urine drug test at screening * Unwillingness or inability to comply with study requirements, including self-administration of study medication, or history of noncompliance in prior clinical trials
Study design
Enrollment target: 108 participants
Allocation: randomized
Masking: quadruple
Age groups: adult, older_adult
Timeline
Starts: 2026-08-17
Estimated completion: 2030-01-01
Last updated: 2026-08-24
Interventions
Drug: AdalimumabDrug: Placebo
Primary outcomes
  • Change in Parkinson Disease Related Pattern (PDRP) expression (Baseline and Week 96)
Sponsor
Yale University · other
With: The Marcus Foundation, National Institute on Aging (NIA), University of Rochester - Center for Health + Technology (CHeT)/Clinical Trials Coordinaton Center (CTCC), The Parkinson Study Group
Contacts & investigators
ContactErika Renkl · contact · erika.renkl@yale.edu · 475-254-9169
ContactKathy Gerich · contact · katherine_gerich@URMC.rochester.edu
InvestigatorJesse Cedarbaum, MD · principal_investigator, Yale University
All locations (19)
Cedars Sinai Medical CenterNot Yet Recruiting
Los Angeles, California, United States
University of Colorado AnschutzRecruiting
Aurora, Colorado, United States
Yale MedicineNot Yet Recruiting
North Haven, Connecticut, United States
Parkinson's Disease & Movement Disorders Center of Boca RatonNot Yet Recruiting
Boca Raton, Florida, United States
Emory University School of MedicineNot Yet Recruiting
Atlanta, Georgia, United States
Johns Hopkins UniversityNot Yet Recruiting
Baltimore, Maryland, United States
Massachusetts General HospitalRecruiting
Boston, Massachusetts, United States
Beth Israel Deaconess Medical CenterNot Yet Recruiting
Boston, Massachusetts, United States
University of MinnesotaNot Yet Recruiting
Minneapolis, Minnesota, United States
Washington UniversityNot Yet Recruiting
St Louis, Missouri, United States
Cleveland Clinic Lou Ruvo Center for Brain Health - Las VegasNot Yet Recruiting
Las Vegas, Nevada, United States
Dartmouth Hitchcock Medical CenterNot Yet Recruiting
Lebanon, New Hampshire, United States
Weill Medical College of Cornell UniversityNot Yet Recruiting
New York, New York, United States
Oregon Health & Science UniversityNot Yet Recruiting
Portland, Oregon, United States
University of PennsylvaniaNot Yet Recruiting
Philadelphia, Pennsylvania, United States
Medical University of South CarolinaNot Yet Recruiting
Charleston, South Carolina, United States
University of Texas Houston Medical CenterNot Yet Recruiting
Houston, Texas, United States
University of Texas Health Science Center- San AntonioNot Yet Recruiting
San Antonio, Texas, United States
Montreal Neurological Institute-Hospital at McGill UniversityNot Yet Recruiting
Montreal, Quebec, Canada