- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT04654468
Uno studio che valuta l'efficacia, la sicurezza, la farmacocinetica e la farmacodinamica di crovalimab nei partecipanti con emoglobinuria parossistica notturna (PNH) non precedentemente trattati con l'inibizione del complemento (COMMODORE 3)
Uno studio di fase III, multicentrico, a braccio singolo che valuta l'efficacia, la sicurezza, la farmacocinetica e la farmacodinamica di crovalimab in pazienti con emoglobinuria parossistica notturna (PNH) non trattati in precedenza con l'inibizione del complemento
This study will enroll participants aged 12 years or older with a body weight ≥ 40 kilograms (kg) diagnosed with PNH who have not been previously treated with complement inhibitor therapy. Approximately 50 participants will be treated with Crovalimab for at least 24 weeks.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 3
Contatti e Sedi
Luoghi di studio
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Chengdu, Cina, 610041
- West China Hospital, Sichuan University
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Guangzhou, Cina, 510115
- Guangdong General Hospital
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Tianjin, Cina, 300052
- Tianjin Medical University General Hospital
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Tianjin, Cina, 300020
- Institute of Hematology and Hospital of Blood Disease
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Hubei
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Wuhan, Hubei, Cina, 430022
- Union Hospital Tongji Medical College Huazhong University of Science and Technology
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Body weight ≥ 40 kg at screening
- Willingness and ability to comply with all study visits and procedures
- Documented diagnosis of PNH, confirmed by high sensitivity flow cytometry
- LDH Levels ≥ 2x the ULN at screening
- Participants who have at least four transfusions during 12 months prior to screening (documented in the medical record)
- Presence of one or more of the PNH-related signs or symptoms within 3 months of screening
- Vaccination against Neisseria meningitidis serotypes A, C, W, and Y < 3 years prior to initiation of study treatment (Day 1)
- Vaccination against Haemophilius influenzae type B and Streptococcus pneumonia according to national vaccination recommendations
- For participants receiving other therapies (e.g., immunosuppressants, corticosteroids): stable dose for ≥ 28 days prior to screening and up to the first drug administration
- Adequate hepatic and renal function
- Women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraception during the treatment period and for 46 weeks (approximately 10.5 months) after the final dose of crovalimab
- Platelet count ≥30,000 per cubic millimeter (mm^3) at screening
- ANC > 500/microlitres (μl) at screening
Exclusion Criteria:
- Current or previous treatment with a complement inhibitor
- History of allogeneic bone marrow transplantation
- History of Neisseria meningitidis infection within 6 months prior to screening and up to first drug administration
- Known or suspected immune or hereditary complement deficiency
- Known HIV infection with cluster of differentiation 4 (CD4) count < 200 cells/µl within 24 weeks prior to screening
- Infection requiring hospitalization or treatment with IV antibiotics within 28 days prior to screening and up to the first drug administration, or oral antibiotics within 14 days prior to screening and up to the first drug administration
- Active systemic bacterial, viral, or fungal infection within 14 days before first drug administration
- Presence of fever (≥ 38˚C) within 7 days before the first drug administration
- Splenectomy < 6 months before screening
- History of malignancy within 5 years prior to screening and up to the first drug administration
- Pregnant or intending to become pregnant during the study or within 46 weeks (10.5 months) after the final dose of study treatment
- Participation in another interventional treatment study with an investigational agent or use of any experimental therapy within 28 days of screening or within 5 half-lives of that investigational product, whichever is greater
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
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Sperimentale: Crovalimab
Participants will receive a loading series of crovalimab comprised of an intravenous (IV) dose on Day 1, followed by weekly crovalimab subcutaneous (SC) doses for 4 weeks on Week 1 Day 2, then on Weeks 2, 3, and 4. Maintenance SC dosing will begin at Week 5 and will continue Q4W (every 4 weeks) thereafter for a total of 24 weeks of study treatment. After 24 weeks of crovalimab treatment, participants who derive benefit from the drug may continue to receive crovalimab. |
Crovalimab will be administered at a dose of 1000 milligrams (mg) IV (for participants with body weight between 40 and 100 kg) or 1500 mg IV (for participants with body weight ≥ 100 kg) on Week 1 Day 1. On Week 1 Day 2 and on Weeks 2, 3 and 4, it will be administered at a dose of 340 mg SC. For Week 5 and Q4W thereafter, it will be administered at a dose of 680 mg SC (for participants with body weight between 40 and 100 kg) or 1020 mg SC (for participants with body weight ≥ 100 kg). Dosing schedule will be as described above. |
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Mean Percentage of Participants With Hemolysis Control
Lasso di tempo: From Week 5 up to Week 25
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A Generalized Estimating Equation (GEE) was used to estimate the population-average percentage of the participants with hemolysis control (measured by lactate dehydrogenase (LDH) ≤1.5 x upper limit of normal (ULN)) from Week 5 to Week 25 taking account of the intra-patient and inter-patient correlation between LDH control statuses across visits. The dependent variable was the binary indicator for hemolysis control. Independent variables are categorical effects of visits, continuous baseline LDH. |
From Week 5 up to Week 25
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Difference in Percentage of Participants With Transfusion Avoidance (TA) From Baseline Through Week 25 and Within 24 Weeks Prior to Screening
Lasso di tempo: 24 Weeks Prior to Screening, Baseline to Week 25
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TA was defined as participants who were packed red blood cell (pRBC) transfusion-free and did not require transfusion per protocol-specified guidelines. TA within 24 weeks prior to screening was based on the pRBC transfusion history in the medical records. Reported in this outcome measure is the difference in the percentage of participants between "baseline through Week 25" and "within 24 weeks prior to screening". 95% Confidence Interval (CI) for the difference between the percentage of participants with transfusion avoidance between Pre-screening and Post-baseline is calculated using the Newcombe method. Screening= Day -28 to Day -1 and Baseline= Day 1. |
24 Weeks Prior to Screening, Baseline to Week 25
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Variazione nel tempo della concentrazione totale e libera di C5
Lasso di tempo: Fino a 7 anni
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Fino a 7 anni
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Percentuale di partecipanti con eventi avversi (EA)
Lasso di tempo: Fino a 7 anni
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Fino a 7 anni
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Percentuale di partecipanti con reazioni al sito di iniezione, reazioni correlate all'infusione, ipersensibilità e infezioni (compresa la meningite meningococcica)
Lasso di tempo: Fino a 7 anni
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Fino a 7 anni
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Percentuale di partecipanti con eventi avversi (AE) che hanno portato all'interruzione del farmaco in studio
Lasso di tempo: Fino a 7 anni
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Fino a 7 anni
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Concentrazione sierica minima di Crovalimab nel tempo
Lasso di tempo: Fino a 7 anni
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Fino a 7 anni
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Concentrazioni sieriche di Crovalimab
Lasso di tempo: Fino a 7 anni
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Fino a 7 anni
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Percentuale di partecipanti con anticorpi anti-farmaco (ADA) a Crovalimab
Lasso di tempo: Fino a 7 anni
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Fino a 7 anni
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Attività del complemento terminale misurata mediante analisi immunologica dei liposomi (LIA)
Lasso di tempo: Fino a 7 anni
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Fino a 7 anni
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Valore osservato nella conta assoluta dei reticolociti
Lasso di tempo: Fino a 7 anni
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Fino a 7 anni
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Valore osservato in emoglobina libera
Lasso di tempo: Fino a 7 anni
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Fino a 7 anni
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Valore osservato nell'aptoglobina
Lasso di tempo: Fino a 7 anni
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Fino a 7 anni
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Variazione percentuale rispetto al basale nella conta assoluta dei reticolociti
Lasso di tempo: Basale, settimana 25
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Basale, settimana 25
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Variazione percentuale rispetto al basale dell'emoglobina libera
Lasso di tempo: Basale, settimana 25
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Basale, settimana 25
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Variazione percentuale rispetto al basale nell'aptoglobina
Lasso di tempo: Basale, settimana 25
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Basale, settimana 25
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Percentage of Participants With Breakthrough Hemolysis (BTH)
Lasso di tempo: Baseline, Week 25
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BTH was defined as at least one new or worsening symptom or sign of intravascular hemolysis (fatigue, hemoglobinuria, abdominal pain, shortness of breath [dyspnea], anemia [hemoglobin < 10 grams per deciliter (g/dL)], major adverse vascular event [MAVE, including thrombosis], dysphagia, or erectile dysfunction) in the presence of elevated LDH ≥2xULN after a prior LDH reduction to ≤1.5xULN from the start of study treatment. As pre-specified in the SAP participants withdrawing before Week 25 were deemed to have experienced a BTH event. Percentages have been rounded off to the first decimal point. |
Baseline, Week 25
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Percentage of Participants With Stabilized Hemoglobin
Lasso di tempo: Baseline, Week 25
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Stabilized hemoglobin was defined as avoidance of a ≥2 g/dL decrease in hemoglobin level from baseline, in the absence of transfusion. As pre-specified in the SAP participants withdrawing before Week 25 were deemed to not have hemoglobin stabilization. |
Baseline, Week 25
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Change From Baseline in Fatigue in Adults Aged >=18 Years
Lasso di tempo: Baseline, Week 2, Week 5, Week 9, Week 17, Week 25
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Fatigue was assessed using functional assessment of chronic illness therapy-fatigue (FACIT-F) scale. FACIT-F is a self-assessment questionnaire with a 7-day recall period and 13 items evaluating fatigue and its impact on daily life activities. Items are scored on a response scale that ranges from 0 ("not at all") to 4 ("very much so"). Relevant items are reverse scored, and all the items are summed to create a total score range from 0 to 52, with 0 being the worst possible score and 52 being the best possible score. A higher score indicates low fatigue severity. A positive mean change indicates improvement. FACIT-F was assessed in adult participants only. FACIT-F assessment was unintentionally missed in the Schedule of Activities (SoA) table, which site used to guide the assessments at each timepoint. Therefore, data were not collected at Week 25. |
Baseline, Week 2, Week 5, Week 9, Week 17, Week 25
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Collaboratori e investigatori
Sponsor
Investigatori
- Direttore dello studio: Clinical Trials, Hoffmann-La Roche
Pubblicazioni e link utili
Pubblicazioni generali
- Roth A, Fu R, He G, Alzahrani H, Chou SC, Hicheri Y, Kazmierczak M, Recova VL, Uchiyama M, Vladareanu AM, Beveridge L, Buatois S, Buri M, Compagno N, Shi D, Balachandran N, Sreckovic S, Scheinberg P. Safety of Crovalimab Versus Eculizumab in Patients With Paroxysmal Nocturnal Haemoglobinuria (PNH): Pooled Results From the Phase 3 COMMODORE Studies. Eur J Haematol. 2025 Feb;114(2):373-382. doi: 10.1111/ejh.14339. Epub 2024 Nov 13.
- Liu H, Xia L, Weng J, Zhang F, He C, Gao S, Jia J, Chang AC, Lundberg P, Shi J, Sima CS, Sostelly A, Sreckovic S, Xiao Z, Zhang Z, Fu R. Efficacy and safety of the C5 inhibitor crovalimab in complement inhibitor-naive patients with PNH (COMMODORE 3): A multicenter, Phase 3, single-arm study. Am J Hematol. 2023 Sep;98(9):1407-1414. doi: 10.1002/ajh.26998. Epub 2023 Jul 8.
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Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- YO42311
Piano per i dati dei singoli partecipanti (IPD)
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Descrizione del piano IPD
For eligible studies, qualified researchers may request access to individual patient level clinical data. See Roche's commitment to transparency of clinical study information here: https://go.roche.com/data_sharing
Informazioni su farmaci e dispositivi, documenti di studio
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .