Iptacopan History and Updates

68 events · 2018 – present

Synced daily from openFDA and ClinicalTrials.gov. Last sync: .

5
FDA Approvals
1
Label Revisions
62
Trial Milestones
0
Pivotal Publications
Iptacopan — history and updatesFDA approvals, label revisions, recalls, trials, and pivotal publicationsFDA approvalsLabel revisionsRecalls + safetyTrialsPublications2018201920202021202220232024202520262027202820292030Trial: NCT07347990 2026-01-01 → 2027-12-31 (primary completion)Trial: NCT06994845 2025-11-27 → 2030-06-28 (primary completion)Trial: NCT06903234 2025-03-31 → 2029-10-01 (primary completion)Trial: NCT06847607 2025-03-01 → 2025-10-30 (primary completion)Trial: NCT06797518 2025-02-21 → 2027-11-27 (primary completion)Trial: NCT06388941 2024-08-05 → 2026-12-30 (primary completion)Trial: NCT06517758 2024-07-31 → 2027-04-30 (primary completion)Trial: NCT05935215 2024-02-28 → 2028-07-21 (primary completion)Trial: NCT05755386 2023-10-02 → 2028-10-27 (primary completion)Trial: NCT05630001 2023-04-24 → 2024-10-17 (primary completion)Trial: NCT05268289 2022-08-10 → 2026-03-19 (primary completion)Trial: NCT05230537 2022-02-17 → 2026-10-01 (primary completion)Trial: NCT04889430 2022-01-17 → 2026-04-11 (primary completion)Trial: NCT05086744 2021-12-21 → 2023-09-20 (primary completion)Trial: NCT05078580 2021-11-10 → 2022-06-20 (primary completion)Trial: NCT04817618 2021-07-28 → 2027-01-29 (primary completion)Trial: NCT04747613 2021-07-27 → 2027-10-18 (primary completion)Trial: NCT04820530 2021-07-19 → 2022-11-02 (primary completion)Trial: NCT03439839 2018-04-09 → 2020-04-22 (primary completion)FDA approval — 2023-12-05 FDA approved Fabhalta (iptacopan) (NDA 218276) Sponsor: NOVARTIS. Class: Type 1 - New Molecular Entity.FDA approval (supplemental) — 2024-03-26 FDA approved supplemental application for Fabhalta (iptacopan) — Labeling (NDA 218276 S-2) Sponsor: NOVARTIS. Class: Labeling.FDA approval (supplemental) — 2024-05-24 FDA approved supplemental application for Fabhalta (iptacopan) — REMS (NDA 218276 S-3) Sponsor: NOVARTIS. Class: REMS.FDA approval (supplemental) — 2024-08-07 FDA approved supplemental application for Fabhalta (iptacopan) — Efficacy (NDA 218276 S-1) Sponsor: NOVARTIS. Class: Efficacy.FDA approval (supplemental) — 2025-03-20 FDA approved supplemental application for Fabhalta (iptacopan) — Efficacy (NDA 218276 S-4) Sponsor: NOVARTIS. Class: Efficacy.Label revision — 2026-06-08 Boxed warning present on label on FABHALTA label (effective 2026-06-08) WARNING: SERIOUS INFECTIONS CAUSED BY ENCAPSULATED BACTERIA FABHALTA, a complement inhibitor, increases the risk of serious infections, especially those caused by encapsulated bacteria, such as Streptococcus pneumoniae, Neisseria meningitidResults posted — 2023-11-15 Trial results posted: NCT04820530 Study of Efficacy and Safety of Twice Daily Oral Iptacopan (LNP023) in Adult PNH Patients Who Are Naive to Complement Inhibitor TherapyResults posted — 2024-01-03 Trial results posted: NCT03439839 Study of Safety, Efficacy, Tolerability, Pharmacokinetics and Pharmacodynamics of LNP023 in in Patients With Paroxysmal Nocturnal HemoglobinResults posted — 2025-03-19 Trial results posted: NCT05086744 Basket Study to Assess Efficacy, Safety and PK of Iptacopan (LNP023) in Autoimmune Benign Hematological DisordersResults posted — 2025-12-15 Trial results posted: NCT05630001 Single Arm, Open Label Trial With Iptacopan Treatment for 24 Weeks, in Patients on Stable Regimen of Anti-C5 Who Switch to Iptacopan.today (2026-06-11)FDA approvalLabel revisionRecall or safetyTrial activityPivotal publication

Source: openFDA, ClinicalTrials.gov via AACT, PubMed · Hipa.ai, 2026-06-11Download chart as PNG

This page tracks every FDA action, clinical trial milestone, and major publication for Iptacopan since 2018, drawn from openFDA, ClinicalTrials.gov, and PubMed.

All published updates (5)

Upcoming & expected milestones

Primary completion· ClinicalTrials.gov
A Phase III Study to Investigate Efficacy, Safety and Tolerability of Iptacopan Compared With Placebo in Participants Aged 18 to 85 Years Wi
Primary completion· ClinicalTrials.gov
Study to Evaluate the Impact of Iptacopan on Top of SOC on Biopsy Changes in Kidneys of Adult Patients With IgAN
Primary completion· ClinicalTrials.gov
Safety and Efficacy of Iptacopan in Patients With High-Risk Transplantation-Associated Thrombotic Microangiopathy
Primary completion· ClinicalTrials.gov
Efficacy and Safety of Switching From Anti-C5 Antibody Treatment to Iptacopan Treatment in Study Participants With Atypical Hemolytic Uremic
Primary completion· ClinicalTrials.gov
Post-authorization Safety Study of Iptacopan in Adult Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) Using Data From the IPIG PNH R
Primary completion· ClinicalTrials.gov
Study to Assess the Efficacy, Pharmacokinetics, Safety and Tolerability of Iptacopan in Pediatric Patients With Primary IgAN

Past events

2026
Primary completion· ClinicalTrials.gov
Efficacy and Safety of Iptacopan (LNP023) in Adult Patients With Atypical Hemolytic Uremic Syndrome Naive to Complement Inhibitor Therapy
Trial started· ClinicalTrials.gov
Safety and Efficacy of Iptacopan in Patients With High-Risk Transplantation-Associated Thrombotic Microangiopathy
2025
Results posted· ClinicalTrials.gov
Single Arm, Open Label Trial With Iptacopan Treatment for 24 Weeks, in Patients on Stable Regimen of Anti-C5 Who Switch to Iptacopan.
Trial started· ClinicalTrials.gov
Study to Assess the Efficacy, Pharmacokinetics, Safety and Tolerability of Iptacopan in Pediatric Patients With Primary IgAN
Primary completion· ClinicalTrials.gov
A Multicenter Prospective Study of Iptacopan in the Treatment of Refractory/Relapsed Autoimmune Hemolytic Anemia (AIHA)
Trial started· ClinicalTrials.gov
Post-authorization Safety Study of Iptacopan in Adult Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) Using Data From the IPIG PNH R
Results posted· ClinicalTrials.gov
Basket Study to Assess Efficacy, Safety and PK of Iptacopan (LNP023) in Autoimmune Benign Hematological Disorders
Trial started· ClinicalTrials.gov
A Multicenter Prospective Study of Iptacopan in the Treatment of Refractory/Relapsed Autoimmune Hemolytic Anemia (AIHA)
Trial started· ClinicalTrials.gov
Study to Evaluate the Impact of Iptacopan on Top of SOC on Biopsy Changes in Kidneys of Adult Patients With IgAN
2024
Primary completion· ClinicalTrials.gov
Single Arm, Open Label Trial With Iptacopan Treatment for 24 Weeks, in Patients on Stable Regimen of Anti-C5 Who Switch to Iptacopan.
Trial started· ClinicalTrials.gov
A Phase III Study to Investigate Efficacy, Safety and Tolerability of Iptacopan Compared With Placebo in Participants Aged 18 to 85 Years Wi
Trial started· ClinicalTrials.gov
Efficacy and Safety of Switching From Anti-C5 Antibody Treatment to Iptacopan Treatment in Study Participants With Atypical Hemolytic Uremic
Results posted· ClinicalTrials.gov
Study of Safety, Efficacy, Tolerability, Pharmacokinetics and Pharmacodynamics of LNP023 in in Patients With Paroxysmal Nocturnal Hemoglobin
2023
Results posted· ClinicalTrials.gov
Study of Efficacy and Safety of Twice Daily Oral Iptacopan (LNP023) in Adult PNH Patients Who Are Naive to Complement Inhibitor Therapy
Primary completion· ClinicalTrials.gov
Basket Study to Assess Efficacy, Safety and PK of Iptacopan (LNP023) in Autoimmune Benign Hematological Disorders
Trial started· ClinicalTrials.gov
Single Arm, Open Label Trial With Iptacopan Treatment for 24 Weeks, in Patients on Stable Regimen of Anti-C5 Who Switch to Iptacopan.
2022
Primary completion· ClinicalTrials.gov
Study of Efficacy and Safety of Twice Daily Oral Iptacopan (LNP023) in Adult PNH Patients Who Are Naive to Complement Inhibitor Therapy
Trial started· ClinicalTrials.gov
Study of Efficacy and Safety of LNP023 in Participants With Active Lupus Nephritis Class III-IV, +/- V
Primary completion· ClinicalTrials.gov
Pharmacokinetic (PK) and Safety Study of Iptacopan (LNP023) in Participants With Mild, Moderate, and Severe Hepatic Impairment Compared to M
Trial started· ClinicalTrials.gov
A Masked, Placebo-controlled Study to Assess Iptacopan in Age-related Macular Degeneration
Trial started· ClinicalTrials.gov
Efficacy and Safety of Iptacopan (LNP023) in Adult Patients With Atypical Hemolytic Uremic Syndrome Naive to Complement Inhibitor Therapy
2021
Trial started· ClinicalTrials.gov
Basket Study to Assess Efficacy, Safety and PK of Iptacopan (LNP023) in Autoimmune Benign Hematological Disorders
Trial started· ClinicalTrials.gov
Pharmacokinetic (PK) and Safety Study of Iptacopan (LNP023) in Participants With Mild, Moderate, and Severe Hepatic Impairment Compared to M
Trial started· ClinicalTrials.gov
Long-term Safety and Tolerability of Iptacopan in Patients With Paroxysmal Nocturnal Hemoglobinuria
Trial started· ClinicalTrials.gov
Study of Efficacy and Safety of Twice Daily Oral Iptacopan (LNP023) in Adult PNH Patients Who Are Naive to Complement Inhibitor Therapy
2020
Primary completion· ClinicalTrials.gov
Study of Safety, Efficacy, Tolerability, Pharmacokinetics and Pharmacodynamics of LNP023 in in Patients With Paroxysmal Nocturnal Hemoglobin
2018
Trial started· ClinicalTrials.gov
Study of Safety, Efficacy, Tolerability, Pharmacokinetics and Pharmacodynamics of LNP023 in in Patients With Paroxysmal Nocturnal Hemoglobin

Sources

FDA approvals, label revisions, and recalls come from the public openFDA APIs (Drugs@FDA, Drug Label, Drug Enforcement). Drug-safety communications come from the FDA RSS feed. Trial milestones come from ClinicalTrials.gov via the AACT pg dump. Pivotal-publication events come from PubMed, filtered to high-impact journals linked to a Phase 3 trial in our inventory.