A Pilot Study of Inosine in Amyotrophic Lateral Sclerosis (ALS)

Completed · Phase 1

Conditions studied: Amyotrophic Lateral Sclerosis

In brief

This is a single center, open label, 12-week study of inosine treatment. Inosine treatment leads to an increase in the levels of urate (uric acid) in the blood. The primary objective of the study is to determine the tolerability of oral administration of inosine. Secondary study objectives include the measurement of biomarkers of oxidative stress and damage in response to inosine treatment.

Key facts

Study ID

NCT02288091

Run by

Massachusetts General Hospital

People needed

32

Starts

2015-01-01

Expected to finish

2016-03-01

Last updated by the study team

2017-11-06

Who can join

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

You may qualify if…

• Age 18 years or older.
• Sporadic or familial ALS diagnosed as possible, laboratory-supported probable, probable, or definite as defined by revised El Escorial criteria (Appendix 1).
• Capable of providing informed consent and following trial procedures.
• Serum urate < 5.5 mg/dl at screening (i.e. below the population median serum urate levels).
• Willingness to undergo magnetic resonance spectroscopy (MRS) at Baseline and at Week 12 of the study.
• Women must not be able to become pregnant (e.g. post menopausal, surgically sterile, or using adequate birth control methods) for the duration of the study and 3 months after study completion. Adequate contraception includes: abstinence, hormonal contraception (oral contraception, implanted contraception, injected contraception or other hormonal (patch or contraceptive ring, for example) contraception), intrauterine device (IUD) in place for ≥ 3 months, barrier method in conjunction with spermicide, or another adequate method.

You may not qualify if…

• History of urolithiasis.
• Urine pH < 5.5 at screening (as acidic urine is a major determinant of uric acid urolithiasis).
• Urate crystalluria at Screening.
• History of gout.
• History of stroke or myocardial infarction.
• History of symptomatic coronary artery disease (e.g. angina pectoris) or symptomatic peripheral arterial disease within 1 year prior to Screening.
• Symptomatic congestive heart failure with a documented ejection fraction below 45%.
• Poorly controlled arterial hypertension (SBP>160mmHg or DBP>100mmHg at Screening).
• Contraindications to undergo magnetic resonance spectroscopy (MRS) at Baseline and at Week 12 of the study such as history of claustrophobia, inability to lie flat for approximately one hour, or metal implants (metal pins or plates, extensive non-removable dental work, cerebral aneurysm clips, pacemaker).
• Women who are pregnant or lactating.
• The presence of unstable psychiatric disease, cognitive impairment, or dementia that would impair ability of the subject to provide informed consent, according to PI judgment, or a history of active substance abuse within the prior year.
• Anything that, in the opinion of the investigator, would place the subject at increased risk or preclude the subject's full compliance with or completion of the study.
• Use of the following within 30 days prior to Screening: inosine, allopurinol, probenecid, more than 300mg vitamin C daily (note that a subject may take a standard multivitamin up to one tablet or capsule daily). Use of thiazides is permissible as long as the subject is on a stable dose from 1 week prior to Screening.
• Known hypersensitivity or intolerability to inosine.

Where it is running

• Massachusetts General Hospital — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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