Study to Evaluate NRCT-101SR in Adult Attention Deficit Hyperactivity Disorder (ADHD)

Completed · Phase 2/Phase 3 · Has a placebo group

Conditions studied: ADHD

In brief

The goal of this clinical trial is to evaluate the efficacy and safety of NRCT-101SR compared to placebo in adult patients with ADHD aged 18 years and older.

Key facts

Study ID

NCT05683249

Run by

Neurocentria, Inc.

People needed

223

Starts

2023-02-25

Expected to finish

2024-01-17

Last updated by the study team

2025-06-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female, ≥ 18 years of age at screening
• Has a primary diagnosis of ADHD according to the Diagnostic and Statistical Manual, Fifth Edition (DSM-5) classification, confirmed with Mini International Neuropsychiatric Interview (MINI) using DSM-5 probes
• AISRS ≥ 26 at screening and baseline, and does not change by more than 25% from screening to baseline, except subjects who stop taking ADHD medication after screening may have an increase of more than 25%
• Has a minimum score of 4 on the CGI-S at baseline
• Must be fluent in English, and capable of reading, writing, and communicating effectively with others and willing to participate in laboratory classroom
• Completion of at least 10 years of formal education
• Hearing and Vision ability sufficient to complete cognitive testing, in investigator's opinion
• Willing and able to give informed consent
• Total Body weight (bw) must be ≥ 50 kg and ≤ 105 kg and lean body mass (LBM) must be ≤ 75 kg at screening
• Naïve to stimulant or non-stimulant medications used for the treatment of ADHD or have discontinued stimulants at least 2 weeks and non-stimulants at least 3 weeks prior to randomization

You may not qualify if…

• Subject is functioning below an age-appropriate level intellectually, as judged by the investigator.
• Lifetime history of severe psychiatric symptoms of major depression requiring hospitalization, bipolar disorder, schizophrenia of schizoaffective disorder, hallucinations, or delusions. Severe comorbid disorders such as PTSD, severe obsessive-compulsive disorder, or other symptomatic presentation that, in the opinion of the examining physician, will contraindicate NRCT-101SR treatment or confound efficacy or safety assessments. Subjects with mild to moderate forms of social phobia or dysthymia, for instance, may be included.
• History of seizures (other than infantile febrile seizures), any tic disorder (except transient tic disorder and subject has no episodes for at least 1 year), or a current diagnosis of Tourette's Disorder.
• Recent history (within the past 1 year) of suspected substance abuse or dependence disorder (excluding stable nicotine use) in accordance with DSM-5 criteria. (Note: subject's average nicotine use should not be exceeded during each LC visit)
• Current abnormal thyroid function as defined as abnormal screening thyroid stimulating hormone. Treatment for at least 3 months with a stable dose of thyroid medication is permitted.
• Poor kidney function; corrected estimated glomerular filtration rate (eGFRcorr) < 40 mL/min/m2
• History of significant gastrointestinal disorders, such as chronic diarrhea, irritable bowel syndrome, ulcerative colitis, Crohn's disease, etc.
• Female subjects who are pregnant and/or lactating
• A "yes" answer to "suicidal ideation" item 4 (active suicidal ideation with some intent to act, without specific plan) or item 5 (active suicidal ideation with specific plan and intent) on the Columbia-Suicide Severity Rating Scale (C-SSRS) assessment at screening (in the past 12 months).
• Has history of severe drug allergy or hypersensitivity to the study medication or its excipients.
• Hypermagnesemia; magnesium > 2.5 mg/dL
• Reproduction:
• a. Females of childbearing potential (FOCP) must be either sexually inactive abstinent) or, if sexually active, must agree to use one of the following acceptable birth control methods beginning 30 days prior to the first dose of study drug and throughout the study: i. Simultaneous use of male condom and intra-uterine contraceptive device placed at least 4 weeks prior to first study drug administration ii. Surgically sterile male partner iii. Simultaneous use of male condom and diaphragm with spermicide iv. Established hormonal contraceptive b. Males must: i. Use 2 methods of contraception in combination if his female partner is of childbearing potential; this combination of contraceptive methods must be used from the Baseline Visit to ≥ 1 month after the last dose of study drug, or ii. Have been surgically sterilized prior to the Screening Visit.
• Is currently participating in another clinical trial or has participated in a clinical trial within 30 days prior to the Screening Visit.
• Currently living in an institutional facility such as a nursing home
• Severe physical disability not associated with cognitive function that limits ability to complete testing (e.g., severe tremor, debilitating arthritis, etc.)
• Known history of symptomatic cardiac disease, advanced atherosclerosis, structural cardiac abnormality, cardiomyopathy, serious heart rhythm abnormalities, coronary heart disease, transient ischemic attack or stroke or other serious cardiac problems.
• Known family history of sudden cardiac death or ventricular arrhythmia.
• Serious or unstable clinically important systemic illness or disease that, in the judgment of the investigator, is likely to affect cognitive assessment, deteriorate, or affect the subject's safety or ability to complete the study, including hepatic (e.g., Child-Pugh grade C), renal, gastroenterologic, respiratory, cardiovascular, endocrinologic, immunologic, infectious, or hematologic disorders
• Has previously participated in a NRCT-101SR investigational study or a study that includes the active ingredient of NRCT-101SR
• Investigators and their immediate family members are not permitted to participate in the study.
• Consumes more than a weekly average of: 2 drinks / day or more than 3 drinks in any day for males; 1 drink / day or more than 2 drinks in any day for females
• Changes in medications or doses of medication as follows:
• All allowed concomitant medications, supplements, or other substances must be at stable doses for at least 30 days prior to screening and must be kept as stable as medically possible during the trial. For allowed concomitant medications, any dosing change within 30 days of Screening may be allowed if, in the opinion of the investigator, it will not affect or influence study results.

Where it is running

• Collaborative Neuroscience Network — Garden Grove, California, United States
• Accel Research Sites — Lakeland, Florida, United States
• Accel Research Sites — Maitland, Florida, United States
• Miami Dade Medical Research Institute — Miami, Florida, United States
• Velocity Clinical Research - Meridian — Meridian, Idaho, United States
• Alcanza Clinical Research Company — Boston, Massachusetts, United States
• Center for Psychiatry and Behavioral Medicine — Las Vegas, Nevada, United States
• Hassman Research Institute — Berlin, New Jersey, United States
• Coastal Carolina Research Center - North Charleston — North Charleston, South Carolina, United States

Full record on ClinicalTrials.gov

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