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NCT05230537CompletedPhase 2

A Masked, Placebo-controlled Study to Assess Iptacopan in Age-related Macular Degeneration

A Randomized, Participant and Investigator Masked, Placebo-controlled, Multicenter, Proof-of-concept Study to Assess the Safety and Efficacy of LNP023 (Iptacopan) in Patients With Early and Intermediate Age-related Macular Degeneration

Source: ClinicalTrials.gov · Last updated 27 Oct 2026

Brief summary (registry, in English)

The purpose of this study is to assess the effect of Iptacopan to prevent conversion of early or intermediate age-related macular degeneration (AMD) eyes to new incomplete retinal pigment epithelium and outer retinal atrophy (iRORA) or late AMD.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
168 (actual)
First submitted
28 Jan 2022
Start date
17 Feb 2022
Primary completion date
19 Aug 2026
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT05230537

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 168
  • From 17 Feb 2022 to the primary completion date, 19 Aug 2026
  • 28 sites in 4 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.

Prior treatment

  • History of stroke or myocardial infarction during the 6-month period prior to Baseline/Day 1, any current clinically significant arrhythmias, or any advanced cardiac or severe pulmonary hypertension

Other illness

  • History or current diagnosis of ECG abnormalities indicating significant safety risk, such as clinically significant cardiac arrhythmias, e.g., sustained ventricular tachycardia and clinically significant second or third degree atrioventricular block (AV block) without a pacemaker.
  • History of end stage kidney disease requiring dialysis or renal transplant
  • History of malignancy of any organ system
  • History of solid organ or bone marrow transplantation
  • History of recurrent meningitis or history of meningococcal infections despite vaccination
  • History of immunodeficiency diseases, including a positive Human Immunodeficiency Virus test result at Screening
  • Active Hepatitis B (HBV) or Hepatitis C (HCV) infection
  • History of hypersensitivity to any of the study treatments or excipients or to drugs of similar chemical classes or clinically relevant sensitivity to fluorescein dye as assessed by the Investigator.

Lab values

  • History of familial long QT syndrome or known family history of Torsades de Pointes
  • Participants who have current active TB as evidenced by clinical, radiographic and laboratory tests.

Other

  • Evidence of cRORA or exMNV in the study eye based on multimodal imaging as determined by the central reading center.

Who the study is looking for

  • Male or female participants ≥ 50 years of age
  • Diagnosis of early or intermediate age-related macular degeneration (AMD) in the study eye as determined by the investigator on fundus examination
  • Study eye (early/intermediate AMD eye) must have at least one high risk optical coherence tomography (OCT) feature (as defined by a central reading center).
  • Diagnosis of neovascular AMD (nAMD) in the fellow eye as determined by the investigator.
  • Vaccination against Neisseria meningitidis and Streptococcus pneumoniae infection are required prior to the start of the treatment with LNP023.
  • If not received previously, vaccination against Haemophilius influenzae infection should be given, if available and according to local regulations.

Age in the registry: 50 years to 100 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (28)

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

SiteCityCountrySite status
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HarbinChinaUnknown status
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ShanghaiChinaUnknown status
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TianjinChinaUnknown status
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LondonUnited KingdomUnknown status
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SouthamptonUnited KingdomUnknown status
Emanuelli Research and Development Center, LLC
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AreciboPuerto RicoUnknown status
Austin Research Center for Retina
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AustinUnited StatesUnknown status
Retina Care Center
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BaltimoreUnited StatesUnknown status
Retina Consultants TX Rsrch Ctr
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BellaireUnited StatesUnknown status
Envision Ocular, LLC
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BloomfieldUnited StatesUnknown status
Opthamalic Consultants of Boston
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BostonUnited StatesUnknown status
Midwest Eye Institute
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CarmelUnited StatesUnknown status
Retina Foundation
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DallasUnited StatesUnknown status
Advanced Research LLC
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Deerfield BeachUnited StatesUnknown status
Retina Center Of South Florida
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Delray BeachUnited StatesUnknown status
Southwest Retina Research Center
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DurangoUnited StatesUnknown status
Duke Eye Center
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DurhamUnited StatesUnknown status
Texas Retina Associates
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Fort WorthUnited StatesUnknown status
Retina Consultants of Orange County
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FullertonUnited StatesUnknown status
Charles Retina Institute
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GermantownUnited StatesUnknown status
Retina Consultants of Houston PA
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HoustonUnited StatesUnknown status
Salehi Retina Institute
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Huntington BeachUnited StatesUnknown status
Retina Associates New Orleans
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MetairieUnited StatesUnknown status
Retina Northwest, PC
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PortlandUnited StatesUnknown status
Martel Eye Medical Group
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Rancho CordovaUnited StatesUnknown status
Retinal Consultants Medical Group, Inc.
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SacramentoUnited StatesUnknown status
California Retina Consultants
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Santa BarbaraUnited StatesUnknown status
Retina Vitreous Associates of Florida
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St. PetersburgUnited StatesUnknown status

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