Skip to content

Efficacy of Sialic Acid GNE Related Thrombocytopenia

A Phase 2 Study to Evaluate the Efficacy of Sialic Acid-Extended Release (SA-ER) Tablets in Patients With GNE Related Thrombocytopenia

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02845609
Acronym
SA-thrombo
Enrollment
5
Registered
2016-07-27
Start date
2016-09-30
Completion date
2017-09-30
Last updated
2018-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Thrombocytopenia

Keywords

Congenital macrothrombocytopenia, Sialic acid, Bleeding

Brief summary

Sialic Acid-Extended Release (SA-ER, aceneuramic acid, UX001) is an extended release formulation of sialic acid (SA, also known as N-acetylneuraminic acid or NANA). The SA-ER is currently studied as a substrate replacement therapy for patients with GNE myopathy. The investigators plan to study the SA-ER compound in a cohort of five patients with GNE-related thrombocytopenia.

Detailed description

The investigators identified 5 affected individuals (3 males and 2 females from three families, age 19-40 years) with GNE-related thrombocytopenia . All subjects will receive 2 gram SA-ER, three times per day for a total daily dose of 6 grams (6,000 mg). The dose should be administered with food (i.e. within 30 minutes of a meal or snack). Efficacy will be evaluated by improvement in clinical and laboratory assessments. Results from Baseline assessments will be compared with those of post-treatment assessments with efficacy conclusions based on improvement between Baseline and the last scheduled assessment. Safety will be evaluated by the incidence and frequency of adverse events, including clinically significant changes from Baseline to scheduled time points in: * Vital signs. * History and physical examination findings. * Laboratory evaluations. * Serum uric acid levels and urinary excretion of uric acid.

Interventions

DRUGSialic Acid-Extended Release

Oral drug of Sialic acid

Sponsors

Hadassah Medical Organization
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Patients with GNE-related macrothrombocytopenia in the investigated family

Exclusion criteria

* non consenting for this study * pregnancy

Design outcomes

Primary

MeasureTime frame
Increase in platelet count from baseline3 month

Secondary

MeasureTime frame
Incidence and frequency of AEs and SAEs (Safety)3 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026