A Study of Pegcetacoplan in Pediatric Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Pegcetacoplan.
- Who it may be relevant to
- Registry conditions: Paroxysmal Nocturnal Hemoglobinuria (PNH), Paroxysmal Hemoglobinuria. Basic parameters: 12 years — 17 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States, Czechia, France, Malaysia, Netherlands +4
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
An Open Label, Single-Arm, Phase 2 Study to Evaluate the Safety, Pharmacokinetics, and Biologic Activity of Pegcetacoplan in Pediatric Patients With Paroxysmal Nocturnal Hemoglobinuria
Overview
The purpose of this study is to evaluate the safety, effectiveness, and biological activity (how the investigational medication is processed by the body) of pegcetacoplan in 12-17 year-olds (adolescents) who have paroxysmal nocturnal hemoglobinuria (PNH).
Detailed description
This is an open-label study to evaluate pegcetacoplan in people with PNH who are 12-17 years old. The study will consist of a 4-week screening period followed by a 16-week treatment period. Participants switching from a C5 inhibitor will have an additional 4 week run-in period between the screening and treatment periods. At the completion of the study treatment period, participants will either enter a long-term extension period or a 2-month follow-up period.
All eligible study participants will receive pegcetacoplan, administered via subcutaneous infusion twice a week at home. The subcutaneous infusion requires two small needles to be inserted into the fatty layer of tissue under the skin and the investigational medication will flow into the body. Study participants and/or caregivers will be trained on home administration of pegcetacoplan.
Interventions
- Drug Pegcetacoplan
Complement (C3) inhibitor
Primary outcome measures
- Pegcetacoplan serum concentrations over the course of the 16-week treatment period [Time frame: 16 weeks]
- Change from baseline to Wk 16 in hemoglobin (Hb) [Time frame: 16 weeks]
- Incidence and severity of treatment-emergent adverse events (TEAEs) over the course of the 16-week treatment period, including monitoring bacterial infections [Time frame: 16 weeks]
- Change from baseline to wk 16 lactate dehydrogenase (LDH) [Time frame: 16 weeks]
- Change from baseline to wk 16 absolute reticulocyte count (ARC) [Time frame: 16 weeks]
Secondary outcome measures (9)
- Change from baseline from week 16 to week 52 of C3 deposition on RBC cells [Time frame: Week 16-52]
- Incidence of thromboembolic events (major adverse vascular events [MAVE]) over the course of the 16-week treatment period and over 52 weeks of treatment with pegcetacoplan [Time frame: 52 weeks]
- Occurrence of breakthrough hemolysis over 16 and 52 weeks of treatment with pegcetacoplan [Time frame: Week 16-52]
- Change from baseline to Week 52, and from Week 16 to Week 52 , in Hb [Time frame: Week 16-52]
- Change from baseline to Week 16 and to Week 52 in Health-Related Quality of Life (HRQOL) assessments [Time frame: Week 16-52]
- Number of packed red blood cell (PRBC) units [Time frame: Week 16-52]
- Total units (mL/kg) transfused over 16 and 52 weeks of treatment with pegcetacoplan [Time frame: Week 16-52]
- Change from baseline to Week 52, and from Week 16 to Week 52, in LDH [Time frame: Week 16-52]
- Change from baseline to Week 52, and from Week 16 to Week 52 ARC [Time frame: Week 16-52]
Eligibility criteria
Inclusion criteria
- Are 12-17 years old at the time of screening
- Weigh at least 20 kg (approx. 44 lbs)
- Have the diagnosis of PNH, confirmed by high-sensitivity flow cytometry (granulocyte or monocyte clone >10%)
- EITHER:
- Not being treated with an approved complement inhibitor (eculizumab or ravulizumab) prior to start of pegcetacoplan dosing, AND have hemolytic anemia. Hemolytic anemia is defined as hemoglobin (Hb) less than the lower limit of normal (Hb < LLN) and LDH >1.5 times the upper limit of normal (ULN); OR
- Currently receiving treatment with an approved complement inhibitor (eculizumab or ravulizumab) AND have evidence of ongoing anemia. Ongoing anemia is defined as Hb < LLN and ARC > ULN
- Have a platelet count >75,000/mm3 and an absolute neutrophil count >1000/mm3
Exclusion criteria
- Are an adult, 18 years of age or older, with PNH
- Known or suspected hereditary fructose intolerance (HFI)
- History of hereditary complement deficiency, bone marrow transplant, or meningococcal disease (meningitis, bacteremia or septicemia)
- Females who are pregnant or breastfeeding
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Netherlands · 2 centers
- Radboud University Hospital Nijmegen — Nijmegen
- University Medical Center Utrecht — Utrecht
Spain · 2 centers
- University Hospital Vall d'Hebron — Barcelona
- University Hospital 12 de Octubre — Madrid
Thailand · 2 centers
- Phramongkutklao Hospital and College of Medicine — Bangkok
- Maharaj Nakorn Chiang Mai hospital — Chiang Mai
United States · 1 center
- Children's Hospital of Atlanta — Atlanta
Czechia · 1 center
- Motol University Hospital — Prague
France · 1 center
- Robert-Debré Hospital Paris — Paris
Malaysia · 1 center
- Hospital Ampang — Ampang
Serbia · 1 center
- University Children's Hospital — Belgrade
United Kingdom · 1 center
- St. Mary's Hospital — London
Identifiers
NCT: NCT04901936 · APL2-PNH-209