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NCT01757431
The Safety and Efficacy of Eculizumab in Japanese Patients With Atypical Hemolytic Uremic Syndrome (aHUS)
Phase 2 trial testing Eculizumab in Atypical Hemolytic Uremic Syndrome (aHUS) in 2 participants. Completed in 25 September 2013.
24 September 2013
Quick facts
| Lead sponsor | Alexion Pharmaceuticals, Inc. |
|---|---|
| Phase | Phase 2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 2 |
| Start date | 16 May 2012 |
| Primary completion | 24 September 2013 |
| Estimated completion | 25 September 2013 |
| Sites | 2 locations across Japan |
Drugs / interventions tested
- Eculizumab (ECULIZUMAB) — full drug profile →
Conditions studied
- Atypical Hemolytic Uremic Syndrome (aHUS) — all drugs for Atypical Hemolytic Uremic Syndrome (aHUS) →
Sponsor
Alexion Pharmaceuticals, Inc. — full company profile →
Who can join
Eligibility, any sex, with Atypical Hemolytic Uremic Syndrome (aHUS). Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Protocol is intended to characterize the overall safety and tolerability of eculizumab in this population.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Interventions for atypical haemolytic uraemic syndrome.
Pugh D, O'Sullivan ED, Duthie FA, Masson P, et al · · 2021 · cited 13× · PMID 33783815 · DOI 10.1002/14651858.cd012862.pub2
Verify or expand the search:
- PubMed search for NCT01757431
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Eculizumab
Trials testing the same drug.
- NCT06764160 — Efficacy, Safety, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of Eculizumab in Chinese Adults With gMG · Phase 3 · completed
- NCT06513338 — Complement C5 mAb in the Treatment of Anti-GBM Disease · Phase 2 · completed
- NCT05876351 — Eculizumab in Pediatric and Adult Participants With Atypical Hemolytic Uremic Syndrome (aHUS) in China · Phase 3 · completed
- NCT05886244 — Eculizumab in Adult Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH) in China · Phase 3 · completed
- NCT05131204 — Efficacy and Safety of the Combination of Pozelimab and Cemdisiran Versus Continued Eculizumab or Ravulizumab Treatment · Phase 3 · terminated
Other recruiting trials for Atypical Hemolytic Uremic Syndrome (aHUS)
Currently open trials in the same condition.
- NCT06312644 — Study of Ultomiris® (Ravulizumab) Safety in Pregnancy · recruiting
Other Alexion Pharmaceuticals, Inc. trials
Trials by the same sponsor.
- NCT06015750 — Mitigate Immune-Mediated Loss of Therapeutic Response to Asfotase Alfa (STRENSIQ®) for Hypophosphatasia · Phase 4 · withdrawn
- NCT07352423 — Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Study of ALXN2230 in Healthy Participants · Phase 1 · recruiting
- NCT07221838 — A Study to Investigate OCS Tapering in Adult Participants With Generalized Myasthenia Gravis Treated With Ravulizumab · Phase 4 · recruiting
- NCT07413250 — Assess Long-Term Safety of Danicopan Add-on Therapy in Participants With Paroxysmal Nocturnal Hemoglobinuria: Analysis o · active not recruiting
- NCT07308574 — Post-Marketing Clinical Study of Ravulizumab in Participants With Clinical aHUS · Phase 4 · recruiting
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 NCT01757431 (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 Alexion Pharmaceuticals, Inc.
- Last refreshed: 10 March 2017
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/NCT01757431.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing