NCT07154745RecruitingPhase 3
A Study to Evaluate How Pozelimab + Cemdisiran Combination Therapy Works in Adult Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) Whose Current Treatment is Not Working Efficiently
A Single Arm Study to Evaluate the Efficacy and Safety of Pozelimab and Cemdisiran Combination Therapy in Patients With Paroxysmal Nocturnal Hemoglobinuria With Inadequate Control of Intravascular Hemolysis on Currently Available C5 Inhibitor Therapy
Source: ClinicalTrials.gov · Last updated 5 Aug 2026
Brief summary (registry, in English)
This study is researching a treatment combination with two experimental drugs called pozelimab and cemdisiran referred to as "study drugs". Researchers are looking for a better way to treat Paroxysmal Nocturnal Hemoglobinuria (PNH). The aim of the study is to see how well the pozelimab and cemdisiran combination works to lower hemolysis in participants whose PNH has been not well controlled even after taking other complement component 5 (C5) inhibitors, eculizumab/eculizumab biosimilar, ravulizumab or crovalimab. The study is looking at several other research questions, including: * What side effects may happen from taking the study drugs? * How much of the study drugs are in the blood at different times? * Whether the body makes antibodies against the study drug (which could make the study drugs not work as well or could lead to side effects)
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 35 (estimated)
- First submitted
- 13 Aug 2025
- Start date
- 11 Jun 2026
- Primary completion date
- 18 Jan 2030
- Lead sponsor
- Regeneron Pharmaceuticals
- NCT number
- NCT07154745
- EU CT number
- 2024-519709-37-00
What you commit to
- Study type: Interventional · Phase 3
- Planned participants: 35
- From 11 Jun 2026 to the primary completion date, 18 Jan 2030
- 20 sites in 7 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
- Receipt of an organ transplant, history of bone marrow transplantation or other hematologic transplants
- Any active or ongoing infection within 2 weeks of screening or during the screening period or any recent infection as described in the protocol
Other
- Body weight \<40 kilograms at screening visit
- Patients with a known or suspected C5 mutation that is refractory to their current C5i treatment as described in the protocol
- Known hereditary complement deficiency
- Note: Other protocol-defined Inclusion/ Exclusion Criteria apply
Who the study is looking for
- Diagnosis of PNH confirmed by a history of high-sensitivity flow cytometry from prior testing
- Currently treated with marketed eculizumab, ravulizumab, or crovalimab at the labeled dose for at least 6 months
- LDH persistently \> 1.5 × Upper Limit of Normal (ULN) in the previous 6 months that the Principal Investigator (PI) attributes is due to intravascular hemolysis
- At least 2 screening LDH values from different visits as described in the protocol
- Willing and able to comply with clinic/remote visits and study-related procedures, including completion of the full series of meningococcal vaccinations required per protocol and agreement to continue to remain up to date with these vaccinations during the study
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (20)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hospital das Clinicas da FMRP USP Coordinator of this site? Confirm its status | Ribeirão Preto | Brazil | Recruiting |
| Faculdade de Medicina do ABC Coordinator of this site? Confirm its status | Santo André | Brazil | Recruiting |
| Hospital Santa Marcelina Coordinator of this site? Confirm its status | São Paulo | Brazil | Recruiting |
| CISSS-CA Coordinator of this site? Confirm its status | Lévis | Canada | Recruiting |
| Institut Catala d'Oncologia Coordinator of this site? Confirm its status | Barcelona | Spain | Recruiting |
| Hospital Universitario Basurto Coordinator of this site? Confirm its status | Bilbao | Spain | Recruiting |
| Hospital San Pedro De Alcántara Coordinator of this site? Confirm its status | Cáceres | Spain | Recruiting |
| Hospital General JM Morales Meseguer Coordinator of this site? Confirm its status | Murcia | Spain | Recruiting |
| Hospital Universitario De Salamanca Coordinator of this site? Confirm its status | Salamanca | Spain | Recruiting |
| AOU Careggi Coordinator of this site? Confirm its status | Florence | Italy | Recruiting |
| Universita Cattolica del Sacro Cuore - Policlinico Universitario A. Gemelli Coordinator of this site? Confirm its status | Rome | Italy | Recruiting |
| SC Hematology, AOU Città della Salute e della Scienza di Torino Coordinator of this site? Confirm its status | Torino | Italy | Recruiting |
| Seoul St. Mary's Hospital, The Catholic University of Korea Coordinator of this site? Confirm its status | Seoul | South Korea | Recruiting |
| Severance hospital Coordinator of this site? Confirm its status | Seoul | South Korea | Recruiting |
| Seoul National University Hospital Coordinator of this site? Confirm its status | Seoul | South Korea | Recruiting |
| Samsung Medical Center Coordinator of this site? Confirm its status | Seoul | South Korea | Recruiting |
| Ewha Womans University Mokdong Hospital Coordinator of this site? Confirm its status | Seoul | South Korea | Recruiting |
| In- Vivo Sp. z o. o. Coordinator of this site? Confirm its status | Bydgoszcz | Poland | Recruiting |
| Istanbul University, Istanbul Faculty of Medicine Coordinator of this site? Confirm its status | Istanbul | Turkey (Türkiye) | Recruiting |
| Ege University Coordinator of this site? Confirm its status | Izmir | Turkey (Türkiye) | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.