A Pilot Study of RNS60 in Amyotrophic Lateral Sclerosis (ALS)

Completed · Phase 1

Conditions studied: ALS

In brief

The purpose of this study is to determine the safety and tolerability of RNS60 in patients with Amyotrophic lateral sclerosis (ALS). Investigators will also measure the impact of RNS60 on several markers of neuro-inflammation, measured by blood biomarkers and positron emission tomography (PET) imaging.

Key facts

Study ID

NCT02525471

Run by

Sabrina Paganoni, M.D.

People needed

24

Starts

2015-10-01

Expected to finish

2017-10-18

Last updated by the study team

2021-05-28

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Amyotrophic Lateral Sclerosis (ALS) volunteers must be diagnosed as having possible, probable, probable-laboratory supported, or definite ALS, either sporadic or familial according to modified El Escorial criteria.
• Age 18-80, able to provide informed consent, and comply with study procedures.
• Participants must not have taken riluzole for at least 30 days, or be on a stable dose of riluzole for at least 30 days, prior to screening (riluzole-naïve participants are permitted in the study).
• Women must not be able to become pregnant (e.g. post menopausal, surgically sterile, or using adequate birth control) for the duration of the study and 3 months after study completion.
• Males should practice contraception for the duration of the study and 3 months after completion.
• Ability to safely lie flat for 90 min for Positron Emission Tomography (PET) procedures in the opinion of the study physician.
• High or mixed affinity to bind translocator (TSPO) protein (Ala/Ala or Ala/Thr)

You may not qualify if…

• Abnormal liver function defined as aspartate aminotransferase (AST) and/or alanine transaminase (ALT) > 3 times the upper limit of the normal.
• Renal insufficiency as defined by a serum creatinine > 1.5 times the upper limit of normal.
• The presence of unstable psychiatric disease, cognitive impairment, or dementia that would impair ability of the participant to provide informed consent, according to PI judgment.
• Clinically significant unstable medical condition (other than ALS) that would pose a risk to the participant if they were to participate in the study.
• History of HIV, clinically significant chronic hepatitis, or other active infection.
• Females must not be lactating or pregnant.
• Active participation in another ALS clinical trial within 30 days of the Screening Visit
• Exposure to immunomodulatory medications within 30 days of the Screening Visit.
• Any contraindication to undergo MRI studies such as
• History of a cardiac pacemaker or pacemaker wires
• Metallic particles in the body
• Vascular clips in the head
• Prosthetic heart valves
• Claustrophobia
• Radiation exposure that exceeds the site's current guidelines
• Current use of tobacco products including cigarettes, cigars, snuff and chewing tobacco, or nicotine replacement products such as gum or patch

Where it is running

• Massachusetts General Hospital — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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