Phase I Clinical Trial of ManNAc in Patients With GNE Myopathy or Hereditary Inclusion Body Myopathy (HIBM)

• Status: Completed
• Trial end date: 2013-05-29
• Target enrollment: 0
• Participant gender: All

Summary

Background:

• Hereditary inclusion body myopathy (HIBM) is a genetic disorder caused by mutations in a gene called GNE. This gene is responsible for producing a sugar called sialic acid. Low levels of sialic acid may cause muscle problems. Symptoms of HIBM include walking difficulties and muscle weakness, which usually start in a person s 20s or 30s and become worse over time.

Researchers are studying a drug called ManNAc. It may be useful for treating HIBM. However, this drug is still being tested. Researchers want to see how ManNAc is absorbed into and removed from the blood. They will not be looking specifically at whether ManNAc can stop or slow the symptoms of HIBM.

Objectives:

-To study how MaNAc is absorbed into and removed from the blood in people with HIBM.

• To study of safety of ManNAc in people with HIBM.

Eligibility:

• Individuals between 18 and 70 years of age who have HIBM.

Design:

• Participants will be screened with a physical exam and medical history. Blood and urine samples will be collected.

• Participants will have a 3 to 4-day inpatient stay for the main part of the study.

• Participants will be divided into groups of six. In each group, four will take ManNAc and two will take a placebo. Participants will not know which one they will receive.

• Participants will have a single dose of either ManNAc or placebo. They will be monitored for any possible side effects. Frequent blood samples will be collected during the 4-day stay.

• No treatment for HIBM will be provided as part of this study. Phase: Phase 1Accepts Healthy Volunteers? No

Details

• Lead Sponsor: National Human Genome Research Institute (NHGRI)
• Collaborators: National Center for Advancing Translational Science (NCATS); Therapeutics for Rare and Neglected Diseases (TRND)

Criteria

• INCLUSIONI CRITERIA:

• Subject is 18-70 years, either gender, inclusive.

• Subject has a diagnosis of HIBM (or IBM2, GNE myopathy, DMRV or Nonaka myopathy) based upon a consistent clinical course and identification of 2 GNE mutations. Molecular confirmation of the diagnosis will be obtained for all subjects in the study.

• Subject must be willing to stop any treatment with ManNAc, sialic acid, IVIG, and/or other supplements containing sialic acid (eg, St John s wort, sialyllactose) 30 days prior to randomization and remain off such treatment for the duration of the trial.

• Subject has the ability to travel to the NIH Clinical Center (CC) for admissions.

• Subject (if a woman of reproductive age) must be willing to use an effective method of contraception for the duration of the trial.

• Subject provides written informed consent.

EXCLUSION CRITERIA:

• Subject has a severe disease manifestation that would interfere with the ability to comply with the requirements of this protocol.

• Subject has a psychiatric illness or neurological disease that would interfere with the ability to comply with the requirements of this protocol. This includes, but is not limited to, uncontrolled/untreated psychotic depression, bipolar disorder, schizophrenia, substance abuse or dependence, antisocial personality disorder, or panic disorder.

• Subject has hepatic laboratory parameters (AST, ALT, GGTP), or renal laboratory parameters (creatinine, BUN) greater than 3 times the upper limit of normal.

• Subject has a QTcB >450 msec (males) or QTcB >470 msec (females).

• Subject is anemic (defined as two standard deviations below normal for age and gender).

• Subject shows evidence of clinically significant cardiovascular, pulmonary, hepatic, renal, hematological, metabolic, or gastrointestinal disease, or has a condition that requires immediate surgical intervention.

• Subject is pregnant or breastfeeding at any time during the study.

• Subject has received treatment with another investigational drug, investigational device, or approved therapy for investigational use within 4 weeks of initial screening.

• Subject has a hypersensitivity to ManNAc or in the judgment of the investigator, has a condition that places the subject at increased risk for adverse effects.