L-arginine Study for Persistent Symptoms of Schizophrenia

Sponsor

University of Massachusetts, Worcester (Other)

Overall Status

Withdrawn

CT.gov ID

NCT04054973

Collaborator

(none)

Enrollment

Location

Arm

27.7

Actual Duration (Months)

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this research is to see if daily combination treatment of L-arginine and Kuvan changes brain chemistry in people experiencing schizophrenia as measured by MRS brain scans.

Condition or Disease	Intervention/Treatment	Phase
Schizo Affective Disorder Schizophrenia	Drug: L-arginine Drug: Sapropterin Dihydrochloride	Phase 2

Study Design

Study Type:

Interventional

Actual Enrollment :

0 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Intervention Model Description:

Open-label single arm pilot trial of L-arginine and Kuvan combination therapyOpen-label single arm pilot trial of L-arginine and Kuvan combination therapy

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

An Open-label Feasibility Trial of Adjunctive L-arginine and Tetrahydrobiopterin Combination in Patients With Treatment Resistant Schizophrenia

Actual Study Start Date :

Sep 11, 2019

Actual Primary Completion Date :

Dec 31, 2021

Actual Study Completion Date :

Dec 31, 2021

Arms and Interventions

Arm	Intervention/Treatment
Experimental: L-arginine and Kuvan Open-label single arm study, all participants will be in this group	Drug: L-arginine 6000mg of L-arginine daily for 14 days Drug: Sapropterin Dihydrochloride 800mg of Kuvan daily for 14 days Other Names: Kuvan

Arm

Intervention/Treatment

Experimental: L-arginine and Kuvan

Open-label single arm study, all participants will be in this group

Drug: L-arginine

6000mg of L-arginine daily for 14 days

Drug: Sapropterin Dihydrochloride

800mg of Kuvan daily for 14 days

Other Names:

Kuvan

Outcome Measures

Primary Outcome Measures

Changes in brain chemistry as measured by 1H-MRS scans [14 days]
To demonstrate that L-arginine and tetrahydrobiopterin (BH4) combination targets and alters brain chemistry in patients with TRS (target engagement). The investigators hypothesize that two-week treatment of L-arginine and Tetrahydrobiopterin (as Kuvan) will alter glutamate and GABA levels measured with proton magnetic resonance spectroscopy (1H-MRS).
Incidence of Treatment-Emergent Adverse Events as assessed by patient report [14-days]
The study doctor in conjunction with the study coordinator will conduct a diagnostic interview with the subject at each visit to record the incidence of treatment-emergent adverse events as assessed by patient report.

Secondary Outcome Measures

Change in Positive and Negative Symptom scale (PANSS) from Baseline to Day 14 [14 days]
The PANSS is a 30-item clinician-rated instrument for assessing schizophrenia symptoms. It consists of 3 subscales: positive subscale (7 items), negative subscale (7 items), and general psychopathology subscale (16 items). For each item, symptom severity was rated on a 7-point scale, from 1=absent to 7=extreme. The PANSS total score for each participant was sum of the rating assigned to each of the 30 PANSS items, and ranged from 30 to 210 with a higher score indicating greater severity of symptoms. The reported measure is the change from baseline at until day 14.
Evaluate changes in NO bioavailability in breath from Baseline to Day 14 [14 days]
Will measure change in NO bioavailability in breath using a Sievers NO Analyzer (NOA280i).
Change in blood levels of glutathione (GSH) from baseline to day 14. [14 days]
Blood levels of glutathione (GSH) (uM) will be measured at baseline and day 14 via blood draw. Values of the this biomarker correspond to the bodies inflammatory and oxidative stress response. The results will be analyzed and compared from baseline to day 14 to measure for the effect of L-arginine and BH4 combination treatment on the body's inflammatory and oxidative stress response regulation.
Change in blood levels of high-sensitivity C reactive protein (hsCRP) from baseline to day 14. [14 days]
Blood levels of high-sensitivity C reactive protein (hsCRP) (mg/L) will be measured at baseline and day 14 via blood draw. Values of the this biomarker correspond to the bodies inflammatory and oxidative stress response. The results will be analyzed and compared from baseline to day 14 to measure for the effect of L-arginine and BH4 combination treatment on the body's inflammatory and oxidative stress response regulation.
Change in blood levels of Tumor Necrosis Factor (TNF-α) from baseline to day 14. [14 days]
Blood levels of Tumor Necrosis Factor (TNF-α) (pg/mL) will be measured at baseline and day 14 via blood draw. Values of the this biomarker correspond to the bodies inflammatory and oxidative stress response. The results will be analyzed and compared from baseline to day 14 to measure for the effect of L-arginine and BH4 combination treatment on the body's inflammatory and oxidative stress response regulation.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 65 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Males or Females aged 18-65 years inclusive.
English speaking.
Primary diagnosis of Schizophrenia established by a structured psychiatric evaluation (MINI) based on Diagnostic and Statistical Manual of Mental Disorders Fifth Edition (DSM-V) criteria.
Written informed consent in compliance with 21 CFR part 50 and in accordance with the International Conference on Harmonization (ICH) Good Clinical Practice (GCP) Guidelines.
A Positive and Negative Syndrome Scale (PANSS) (Kay et al 1987) total score ≥ 70 with a score of > 4 on two or more of the following PANSS items: delusions, conceptual disorganization, hallucinatory behavior, suspiciousness, and unusual thought content.
A score of ≥4 on the Clinical Global Impression-Severity (CGI-S) (Guy, 1976).
Must have ongoing antipsychotic treatment for at least 8 weeks, with a stable dose for at least 4 weeks. Antipsychotic medication will not be modified by the research team during the subject's enrollment or participation.
Subjects who have failed to achieve clinically-recognized symptom reduction to at least 1 marketed antipsychotic agent, given at a Physician Desk Reference (PDR)-defined therapeutic dose for ≥ 8 weeks during the past 12 months, will be eligible.
Women of childbearing potential must have a negative pregnancy test performed at screening visit prior to randomization. Women enrolled in this trial must use adequate birth control.
Understands and is able, willing, and (in the opinion of the investigator) likely to fully comply with the study procedures and restrictions.

Exclusion Criteria:

Subjects with a history of renal insufficiency, congestive heart failure, cardiac arrhythmias or history of myocardial infarction, liver cirrhosis, guanidinoacetate methyltransferase deficiency, herpes.
Subjects who are non-English speaking.
Subjects with any clinically significant abnormalities as determined by medical history, physical exam, clinical and lab evaluation suggestive of an underlying disease state that may, in the opinion of the investigator, confound the results of study, increase risk to the subject, or lead to difficulty complying with the protocol.
Subjects with the lab values defined as exclusionary safety values in Table 1.
On medications known to inhibit folate metabolism (e.g., methotrexate).
On medications known to affect NO-mediated vaso-relaxation (e.g., PDE-5 inhibitors such as sildenafil, vardenafil, or tadalafil).
Subjects on nitrates.
Subjects on levodopa.
Subjects on antihypertensive medications (such as ACE inhibitors, angiotensin receptor blockers, isoproterenol, potassium-sparing diuretics).
Subjects on antidiabetes medications.
Subjects on anticoagulant/antiplatelet medications.
Subjects with a current (within the last 3 months) DSM-V diagnosis of alcohol or substance use disorder (excluding nicotine and caffeine) as established by the clinical assessment (MINI) at the screening visit will be excluded.
Tested positive for the urine drug screen.
Subjects at imminent risk of suicide or injury to self or others, as per the opinion of the investigator, or history of significant suicide attempt within the last 6 months as per the Columbia Suicide Severity Rating Scale (C-SSRS).
Subjects that have taken an investigational drug or taken part in a clinical trial within 30 days prior to screening.
Known history of phenylketonuria (PKU).
Known hypersensitivity reactions (such as anaphylaxis and rash) to L-arginine and/or BH4.
Any other reason that, in the opinion of the investigator, would compromise patient safety or integrity of the study.