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NCT04138251: GLYCO-1B
Safety, Efficacy Evaluation of Empagliflozin Administration for Neutropenia in Glycogenosis Type 1b and G6PC3 Deficiency
Phase 2 trial testing Empagliflozin in Glycogen Storage Disease Type I in 5 participants. Status unknown.
30 June 2020
Quick facts
| Lead sponsor | Cliniques universitaires Saint-Luc- Université Catholique de Louvain |
|---|---|
| Phase | Phase 2 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 5 |
| Start date | 20 June 2019 |
| Primary completion | 30 June 2020 |
| Estimated completion | 30 June 2020 |
| Sites | 1 location across Belgium |
Drugs / interventions tested
- Empagliflozin (empagliflozin) — full drug profile →
Conditions studied
- Glycogen Storage Disease Type I — all drugs for Glycogen Storage Disease Type I →
- Glucose 6 Phosphatase Deficiency — all drugs for Glucose 6 Phosphatase Deficiency →
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):
-
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 -
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 -
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 -
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:
- PubMed search for NCT04138251
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Cliniques universitaires Saint-Luc- Université Catholique de Louvain trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04138251 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Cliniques universitaires Saint-Luc- Université Catholique de Louvain
- Last refreshed: 28 October 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04138251.
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