Phase 1/2, First-in-human, Double-blind, Safety, and Efficacy of UX016 in Adults with GNE Myopathy
UCI Specialty Area: Neurology
Principal Investigator:
Tahseen Mozaffar
Official Title:
Phase 1/2, First-in-human, Double-blind, Placebo-controlled Study to Assess Dose, Safety, and Efficacy of UX016 (sialic acid-C16 prodrug) in Adults with GNE Myopathy
A Study On:
Brain - Neurologic/ Psychologic
Myopathy
Neuromuscular Diseases
Study Description
Eligibility
- A confirmed diagnosis of GNEM (also known as distal myopathy with rimmed vacuoles [DMRV], hereditary inclusion body myopathy [HIBM], inclusion body myopathy 2 [IBM2], and Nonaka myopathy in Japan) by Clinical Laboratory Improvement Amendments (CLIA)-certified genetic testing with identification of a disease-associated variant in the gene encoding the GNE/MNK enzyme. Genotyping will not be conducted in this protocol
- Ability to walk a minimum of 20 m independently during Screening. The use of assistive devices and orthotics is allowed.
- Has less than or equal to 80% of normal biceps strength (dominant side) assessed by hand-held dynamometry (HHD) associated with a clinical pattern of weakening in the upper extremity and ability to provide reproducible force in unilateral elbow flexors (dominant side) during HHD testing (unilateral between test variability of less than or equal to 15%) during Screening.
- Willing and able to comply with all study procedures including needle muscle biopsies of the quadriceps muscle.
- From informed consent to after the last dose of study drug, females of childbearing potential and fertile males must consent to use highly effective contraception. If female, agree not to become pregnant and willing to have additional pregnancy testing during the study. Females considered not of childbearing potential include those who have been in menopause for at least 2 years, have had tubal ligation at least 1 year prior to Screening, or who have had a total hysterectomy. If male, agree not to father a child or donate sperm.
- Provide informed consent after the nature of the study has been explained and prior to any research-related procedures.
- Ingestion of N-acetyl-D-mannosamine (ManNAc), SA, or related metabolites, including 6-sialyllactose; intravenous immune globulin; supplements; or anything that can be metabolized to produce significant amounts of SA in the body for the prior 60 days through the end of the study.
- Any changes in diet or exercise routine in the prior 30 days. Subjects are strongly discouraged from making any changes to their diet and exercise routines following enrollment.
- Receiving concomitant oral medications that are substrates for CYP2B6, P-glycoprotein (P-gp) transporters, or breast cancer resistance protein (BCRP) transporters.
- Known hypersensitivity to SA or its excipients that, in the judgment of the Investigator, places the subject at increased risk for adverse effects.
- Any of the following laboratory abnormalities at Screening:
- Alanine aminotransferase (ALT), aspartate aminotransferase (AST), gamma-glutamyl transferase (GGT), or glutamate dehydrogenase (GLDH) greater than 3 × upper limit of normal (ULN)
- Total bilirubin greater than 2 × ULN
- Estimated glomerular filtration rate (eGFR) less than 60 mL/min/1.73 m2 based on cystatin C.
- Men with a Fridericia-corrected QT interval (QTcF) greater than 450 msec and women with a QTcF greater than 460 msec at Screening.
- Presence or history of any condition, laboratory abnormality, or infection that, in the Investigator's judgment, would interfere with participation, pose undue safety risk, or confound interpretation of study results.
- Pregnant or breastfeeding at Screening or planning to become pregnant (self or partner) at any time during the study.
- Use of any investigational product or investigational medical device within 30 days prior to Screening or requirement for any investigational agent prior to completion of all scheduled study assessments.
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