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NCT04138251: GLYCO-1B

Safety, Efficacy Evaluation of Empagliflozin Administration for Neutropenia in Glycogenosis Type 1b and G6PC3 Deficiency

Status unknown Phase 2 Last updated 28 October 2019
What this trial tests

Phase 2 trial testing Empagliflozin in Glycogen Storage Disease Type I in 5 participants. Status unknown.

Timeline
20 June 2019
Primary endpoint
30 June 2020
30 June 2020

Quick facts

Lead sponsorCliniques universitaires Saint-Luc- Université Catholique de Louvain
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment5
Start date20 June 2019
Primary completion30 June 2020
Estimated completion30 June 2020
Sites1 location across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

Cliniques universitaires Saint-Luc- Université Catholique de Louvain — full company profile →

Who can join

Adults 1 to 18, any sex, with Glycogen Storage Disease Type I or Glucose 6 Phosphatase Deficiency. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Treatment of neutropenia of G6PC3 and Glycogenosis type 1b patients with empagliflozin

Publications & conference data

4 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Successful use of empagliflozin to treat neutropenia in two G6PC3-deficient children: Impact of a mutation in SGLT5.
    Boulanger C, Stephenne X, Diederich J, Mounkoro P, et al · · 2022 · cited 33× · PMID 35506446 · DOI 10.1002/jimd.12509
  2. Endocrine involvement in hepatic glycogen storage diseases: pathophysiology and implications for care.
    Rossi A, Simeoli C, Pivonello R, Salerno M, et al · · 2024 · cited 3× · PMID 38556561 · DOI 10.1007/s11154-024-09880-2
  3. The paradox of autoimmunity and autoinflammation in inherited neutrophil disorders - in search of common patterns.
    Krzyzanowski D, Oszer A, Madzio J, Zdunek M, et al · · 2023 · cited 2× · PMID 37350970 · DOI 10.3389/fimmu.2023.1128581
  4. Established and emerging non-cellular therapies in inherited bone marrow failure syndromes.
    Janczar S, Urbański B, Ussowicz M, Mlynarski W. · · 2026 · PMID 41859097 · DOI 10.3389/fimmu.2026.1773574

Verify or expand the search:

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Data sources for this page

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