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NCT04469465CompletedPhase 3

Danicopan as Add-on Therapy to a C5 Inhibitor in Paroxysmal Nocturnal Hemoglobinuria (PNH) Participants Who Have Clinically Evident Extravascular Hemolysis (EVH)(ALPHA)

A Phase 3 Study of Danicopan (ALXN2040) as Add-on Therapy to a C5 Inhibitor (Eculizumab or Ravulizumab) in Patients With Paroxysmal Nocturnal Hemoglobinuria Who Have Clinically Evident Extravascular Hemolysis (EVH)

Source: ClinicalTrials.gov · Last updated 4 May 2025

Brief summary (registry, in English)

The main objective of this study is to evaluate the efficacy of danicopan as add-on therapy to a complement component 5 (C5) inhibitor (eculizumab or ravulizumab) in participants with PNH who have clinically evident EVH.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
86 (actual)
First submitted
9 Jul 2020
Start date
16 Dec 2020
Primary completion date
29 Jun 2022
Lead sponsor
Alexion Pharmaceuticals, Inc.
NCT number
NCT04469465
EudraCT number
2019-003829-18

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 86
  • From 16 Dec 2020 to the primary completion date, 29 Jun 2022
  • 59 sites in 18 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of a major organ transplant or hematopoietic stem cell transplantation (HSCT)
  • Participants with known aplastic anemia or other bone marrow failure that requires HSCT or other therapies including anti-thymocyte globulin and/or immunosuppressants
  • Evidence of human immunodeficiency virus, hepatitis B, or active hepatitis C infection at screening

Lab values

  • Laboratory abnormalities at screening, including:
    • Alanine aminotransferase \>2 x ULN (\>3 x ULN in case of patients with documented liver iron overload defined by serum ferratin values
    • 500 ng/ML)
    • Direct bilirubin \>2 x ULN (unless due to EVH or documented Gilbert's Syndrome)

Other

  • Known or suspected complement deficiency
  • Current evidence of biliary cholestasis
  • Estimated glomerular filtration rate of \<30 milliliters/minute/1.73 meter squared and/or are on dialysis

Who the study is looking for

  • Diagnosis of PNH
  • Clinically Evident EVH defined by:
    • Anemia (Hgb ≤9.5 gram/deciliter) with absolute reticulocyte count ≥120 x 10\^9/liter
  • Receiving an approved C5 inhibitor for at least 6 months prior to Day 1
  • Platelet count ≥30,000/microliters (µL)
  • Absolute neutrophil counts ≥500/μL
  • Documentation of/or willingness to receive vaccinations for N. meningiditis and prophylactic antibiotics as required

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (59)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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BelémBrazilUnknown status
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CuritibaBrazilUnknown status
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GoiâniaBrazilUnknown status
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Porto AlegreBrazilUnknown status
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Rio de de JaneiroBrazilUnknown status
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TorontoCanadaUnknown status
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BrnoCzechiaUnknown status
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UlmGermanyUnknown status
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BarcelonaSpainUnknown status
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Las Palmas de Gran CanariaSpainUnknown status
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MadridSpainUnknown status
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MajadahondaSpainUnknown status
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SevilleSpainUnknown status
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LilleFranceUnknown status
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ParisFranceUnknown status
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PessacFranceUnknown status
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Pierre-BéniteFranceUnknown status
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AirdrieUnited KingdomUnknown status
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LeedsUnited KingdomUnknown status
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LondonUnited KingdomUnknown status
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AthensGreeceUnknown status
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ThessalonikiGreeceUnknown status
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HaifaIsraelUnknown status
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JerusalemIsraelUnknown status
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AvellinoItalyUnknown status
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Bassano del GrappaItalyUnknown status
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FlorenceItalyUnknown status
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MilanItalyUnknown status
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Reggio CalabriaItalyUnknown status
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RomaItalyUnknown status
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Bunkyō CityJapanUnknown status
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FukuokaJapanUnknown status
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Kashiwa-shiJapanUnknown status
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KyotoJapanUnknown status
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Nagakute-shiJapanUnknown status
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Ogaki-shiJapanUnknown status
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OsakaJapanUnknown status
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SayamaJapanUnknown status
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Shibuya-kuJapanUnknown status
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Tanabe-shiJapanUnknown status
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Toyoake-shiJapanUnknown status
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TsukubaJapanUnknown status
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DaejeonSouth KoreaUnknown status
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SeoulSouth KoreaUnknown status
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SuwonSouth KoreaUnknown status
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Kota KinabaluMalaysiaUnknown status
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KuchingMalaysiaUnknown status
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MiriMalaysiaUnknown status
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MaastrichtNetherlandsUnknown status
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GdanskPolandUnknown status
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BangkokThailandUnknown status
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TaipeiTaiwanUnknown status
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ChicagoUnited StatesUnknown status
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DallasUnited StatesUnknown status
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KalamazooUnited StatesUnknown status
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Los AngelesUnited StatesUnknown status
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MilwaukeeUnited StatesUnknown status
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New YorkUnited StatesUnknown status
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WestonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.