Clinical Trials Study
Phase 3
Long-term Safety and Tolerability of Iptacopan in Patients With Paroxysmal Nocturnal Hemoglobinuria
Conditions: Paroxysmal Nocturnal Hemoglobinuria
- Study #:
- NCT04747613
- Last Updated:
- 05/08/2026
- Recruitment Status:
- Active, not recruiting
- Estimated Study Completion Date:
- 10/18/2027
Summary
This study is an open-label, single arm, multicenter, roll-over extension study to characterize long-term safety, tolerability and efficacy of iptacopan and to provide access to iptacopan to patients with PNH who have completed Novartis-sponsored Phase 2 or 3 studies with iptacopan
Age: 18 Years to 100 Years old
Gender: All
Start Date: 07/27/2021
Primary Completion Date (Estimated): 10/18/2027
Study Completion Date (Estimated): 10/18/2027
Accepts Healthy Volunteers: No
Trial Purpose and Description
The purpose of this phase 3 open-label, single arm, multicenter study is to evaluate the long-term safety, tolerability and efficacy of iptacopan in patients with PNH and to provide access to patients who have completed (without tapering down) Phase 2 and Phase 3 trials and derived benefit from iptacopan treatment.
Eligibility Criteria
Age: 18 Years to 100 Years old
Gender: All
Accepts Healthy Volunteers: No
Inclusion criteria:
* Male and female participants ≥ 18 years of age with a diagnosis of PNH who have completed the treatment extension period (without tapering down) of Phase II iptacopan studies (CLNP023X2204, CLNP023X2201), Period 4 of LFG316X2201 or Phase III (CLNP023C12302 and CLNP023C12301) clinical studies at the time point of enrollment visit in this roll over extension.
* Prior vaccinations against Neisseria meningitidis, Streptococcus pneumoniae and Haemophilus influenzae infections
* Per investigator's clinical judgement benefit from continued treatment with iptacopan and has been clinically stable on iptacopan monotherapy for at least 3 months
Exclusion criteria:
* Any comorbidity or medical condition (including but not limited to any active systemic bacterial, viral or fungal infection or malignancy) that, in the opinion of the investigator, could put the subject at increased risk or potentially confound study data.
* History of recurrent invasive infections caused by encapsulated organisms, such as Neisseria meningitidis, Streptococcus pneumoniae or Haemophilus influenzae
* History of hematopoietic stem cell transplantation
Other protocol-defined inclusion/exclusion criteria may apply.
Principal Investigator
Irina Murakhovskaya, MD