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A Study of Efficacy and Safety of FXS6837 in Anti-C5 Treated PNH Patients.

A Multicenter, Single-Arm, Open-Label Phase III Clinical Study Evaluating the Efficacy and Safety of FXS6837 Capsules in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) Who Remain Anemic After Previous Stable Use of the C5 Complement Inhibitor

This is an single arm, open label designed phase III study to evaluate the efficacy and safety of oral FXS6837 capsules in PNH patients with residual anemia despite the stable treatment with anti-C5 antibody.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

About 20 PNH patients who have received eculizumab stably for at least 6 months before first dosing and still have hemoglobin (Hb) < 100 g/L will be eligible to be enrolled. All patients will take FXS6837 capsules for 24 weeks according to protocol to evaluate the efficacy and safety of FXS6837 Capsules in PNH patients who remain anemic after anti-C5 monoclonal antibody therapy. After completing the 24-week treatment, all participants who are assessed by the investigator as potentially continuing to benefit from FXS6837 may voluntarily enter a separate long-term open-label extension stud and continue to receive FXS6837 treatment.

Tipo di studio

Interventistico

Iscrizione (Stimato)

20

Fase

  • Fase 3

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

      • Tianjin, Cina
        • TianJin Medical University General Hospital
        • Contatto:
    • Zhejiang
      • Hangzhou, Zhejiang, Cina
        • First Affiliated Hospital of Zhejiang University
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion criteria: 1. Male or female subjects aged ≥ 18 years at screening; 2. Body weight ≥ 40 kg and body mass index (BMI) ≥ 18 kg/m2 at screening; 3. Diagnosis of PNH at least 6 months before screening and confirmed by high-sensitivity flow cytometry with a PNH RBC and granulocyte/monocyte population size of ≥10% within 6 months before screening or during screening; 4. Have received a stable treatment regimen (dose and dosing interval) with anti-C5 monoclonal antibody (eculizumab) for at least 6 months prior to the first dose; 5. Have at least one blood transfusion record within 3 months before screening, or Hb level persistently < 100 g/L during stable treatment with anti-C5 monoclonal antibody within 3 months before screening (medical history data/laboratory test reports, at least 2 test records with an interval of ≥ 4 weeks); 6. Hb meeting one of the following conditions: (1) Hb concentration < 100 g/L at the first screening visit, and received RBC transfusion therapy due to PNH-related anemia during the screening period; (2) Mean Hb concentration from two measurements during the screening period < 100 g/L and all Hb measurements < 105 g/L during the screening period (these two measurements should be 2 to 6 weeks apart; multiple Hb measurements are allowed during the screening period); 7. Vaccinated against Neisseria meningitidis and Streptococcus pneumoniae before the first dose. If patients have not been previously vaccinated or need booster vaccination (according to local vaccination policies), vaccination should be completed at least 2 weeks before the first dose. If the first dose must occur within 2 weeks after vaccination, prophylactic antibiotic treatment should be used until at least 2 weeks after vaccination; 8. Participants of reproductive potential commit to having no plans for pregnancy or sperm/egg donation from screening until 1 month (female participants) or 3 months (male participants) after the last dose and voluntarily take effective physical contraceptive methods (including partners); 9. Have a detailed understanding of the nature, significance, possible benefits, potential inconveniences, and potential risks of the trial, and voluntarily participate in this clinical trial; Able to communicate well with the investigators and comply with the requirements of the entire study; Signed a written informed consent form. Exclusion criteria: 1. With laboratory evidence of bone marrow failure during screening (reticulocyte count < 100 × 109/L, or platelet count < 30 × 109/L, or neutrophil count < 0.5 × 109/L); Received acute treatment (such as platelet transfusion, granulocyte colony-stimulating factor) for thrombocytopenia or neutropenia within 30 days before screening; 2. Participants receiving other therapies before screening that have not reached the following stable treatment durations:

  • Erythropoietin for at least 8 weeks
  • Immunosuppressants for at least 8 weeks, systemic corticosteroids (≤ 15 mg/day) for at least 4 weeks
  • Iron, vitamin B12, or folic acid supplementation for at least 4 weeks
  • Anticoagulants: Vitamin K antagonists (such as warfarin) used for at least 4 weeks with a stable international normalized ratio (INR) (as determined by the investigator), low molecular weight heparin, oral anticoagulants such as aspirin, rivaroxaban, apixaban, etc., for at least 4 weeks;
  • Hypoxia-inducible factor prolyl hydroxylase inhibitors (HIF-PHI) for at least 8 weeks;
  • Androgens for at least 4 weeks; 3. History of malignant tumors of any organ or system within 5 years before screening (except local basal cell carcinoma of the skin or carcinoma in situ of the cervix), regardless of whether treatment was received and whether there is evidence of local recurrence or metastasis; 4. History of bone marrow/hematopoietic stem cell or solid organ transplantation (such as heart, lung, kidney, liver); 5. History of splenectomy or planned surgery during the study period; 6. Subjects with significantly abnormal liver function at screening: any parameter of alanine aminotransferase (ALT), γ-glutamyl transpeptidase (GGT), or alkaline phosphatase (ALP) > 3 × ULN; 7. Human immunodeficiency virus (HIV) infection (HIV antibody positive), active syphilis infection, hepatitis B virus infection (hepatitis B surface antigen positive), active hepatitis C virus infection, or active tuberculosis infection at screening; 8. Concurrent systemic critical diseases, including but not limited to: advanced heart disease (such as New York Heart Association [NYHA] Class IV), severe lung disease (such as severe pulmonary hypertension [WHO class IV]), active hepatitis, severe kidney disease (estimated glomerular filtration rate [eGFR] < 30 mL/min/1.73 m2 or chronic kidney disease [CKD] stage 4 or dialysis patients), unstable thrombosis, active gastrointestinal hemorrhage, other blood disorders (such as chronic anemia unrelated to PNH), which are deemed unsuitable for study participation by the investigator; 9. Known or suspected by investigators to have immunodeficiency diseases or hereditary complement deficiency; 10. History of Neisseria meningitidis infection; History of ≥ 2 episodes of pneumococcal infection; 11. Detected or suspected (as assessed by the investigator) systemic active bacterial, viral (including COVID-19), or fungal infections within 2 weeks before the first dose; Axillary temperature > 38 °C within 7 days before the first dose; 12. Suspected or known history of allergies to the IMPs or any ingredient in the IMPs; 13. Received any type of live attenuated vaccine within 4 weeks prior to screening, or plan to receive any live attenuated vaccine during the study; 14. Pregnant or lactating women or those with positive pregnancy test results; 15. Previous history of drug abuse or drug use; 16. Participated in other clinical trials of investigational drugs (or are still within 5 half-lives of the drug, whichever is longer) (except eculizumab) or medical device clinical trials within 30 days prior to screening, plans to participate in other clinical trials during the study, or having residual effects as assessed by the investigator; 17. Having diseases or medical conditions that affect drug absorption, distribution, metabolism, and excretion, or may reduce compliance or increase participant risk, such as severe gastrointestinal disease history, major gastrointestinal surgery history, swallowing difficulties, etc., as assessed by the investigator; Participants who may not be able to complete this study for other reasons, or other situations deemed unsuitable for study participation by the investigator.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

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
Sperimentale: FXS6837

100 mg FXS6837 capsule

FXS6837 capsule will be taken orally for 24 weeks

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Proportion of participants with hemoglobin (Hb) level ≥ 120 g/L in at least 3 of 4 measurements between Week18 and Week24 in the absence of RBC transfusion (defined as no RBC transfusion after Week2 through Week24)
Lasso di tempo: 24 weeks from Baseline (Week 18 through Week 24)
24 weeks from Baseline (Week 18 through Week 24)

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
Proportion of participants with an increase from baseline in Hb level of ≥ 20 g/L in at least 3 of 4 measurements between Week18 and Week24 in the absence of RBC transfusion (defined as no RBC transfusion after Week2 through Week24)
Lasso di tempo: 24 weeks from Baseline (Baseline, Week 18 through Week 24)
24 weeks from Baseline (Baseline, Week 18 through Week 24)
Proportion of participants without RBC transfusion during the treatment period from between Week2 to Week24
Lasso di tempo: Week2 to Week24
Week2 to Week24
Change from baseline in Hb as mean of visits between Week18 and Week24
Lasso di tempo: 24 weeks from Baseline (Baseline, Week 18 through Week 24)
24 weeks from Baseline (Baseline, Week 18 through Week 24)
Change from baseline in reticulocyte count during the treatment period from Week18 to Week24
Lasso di tempo: 24 weeks from Baseline (Baseline, Week 18 through Week 24)
24 weeks from Baseline (Baseline, Week 18 through Week 24)
Percent change from baseline in lactate dehydrogenase (LDH) levels during the treatment period from Week18 to Week24
Lasso di tempo: 24 weeks from Baseline(Baseline, Week 18 through Week 24)
24 weeks from Baseline(Baseline, Week 18 through Week 24)
Proportion of participants with LDH ≤ 1.5 × upper limit of normal (ULN) in at least 3 of 4 measurements between Week18 and Week24;
Lasso di tempo: 24 weeks from Baseline (Week 18 through Week 24)
24 weeks from Baseline (Week 18 through Week 24)
Change from baseline in Functional Assessment of Chronic Illness Therapy - Fatigue Scale (FACIT-Fatigue) score during the treatment period from Week18 to Week24
Lasso di tempo: 24 weeks from Baseline (Baseline, Week 18 through Week 24)
24 weeks from Baseline (Baseline, Week 18 through Week 24)
Incidence rate of BTH between Week1 and Week24
Lasso di tempo: up to 24 weeks
up to 24 weeks
Incidence of MAVEs between Week1 and Week24
Lasso di tempo: up to 24 weeks
up to 24 weeks
Safety evaluation: All participants will be observed for any adverse event (AE) during the clinical study.
Lasso di tempo: up to 24 weeks
up to 24 weeks
Population Pharmacokinetics (PK): Maximum Observed Concentration (Cmax) of FXS6837
Lasso di tempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24
Population Pharmacokinetics (PK): Plasma trough concentration (Ctrough) of FXS6837
Lasso di tempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24
Population Pharmacokinetics (PK): Area Under the Concentration-Time Curve (AUC) of FXS6837
Lasso di tempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24
The exposure-response correlation between Steady-State trough Concentration (Ctrough) of FXS6837 and hemoglobin (Hb) level
Lasso di tempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24
The exposure-response correlation between Steady-State trough Concentration (Ctrough) of FXS6837 and lactate dehydrogenase (LDH) level
Lasso di tempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24
The exposure-response correlation between Steady-State trough Concentration (Ctrough) of FXS6837 and Alternative Pathway(AP) activity
Lasso di tempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24
The exposure-response correlation between Steady-State trough Concentration (Ctrough) of FXS6837 and Fragment Bb of Complement Factor B level
Lasso di tempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24
The exposure-response correlation between Steady-State trough Concentration (Ctrough) of FXS6837 and soluble C5b-9 (sC5b-9) level
Lasso di tempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24
The exposure-response correlation between Steady-State trough Concentration (Ctrough) of FXS6837 and PNH granulocyte clone percentage
Lasso di tempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24
The exposure-response correlation between Steady-State trough Concentration (Ctrough) of FXS6837 and PNH monocyte clone percentage
Lasso di tempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24
The exposure-response correlation between Steady-State trough Concentration (Ctrough) of FXS6837 and C3d+PNH red cell clone percentage
Lasso di tempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24
The exposure-response correlation between Steady-State trough Concentration (Ctrough) of FXS6837 and PNH red cell clone percentage
Lasso di tempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

  • Investigatore principale: Rong Fu, Doctor, Tianjin Medical University General Hospital
  • Investigatore principale: Hongyan Tong, First Affiliated Hospital of Zhejiang University

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

26 gennaio 2027

Completamento primario (Stimato)

17 maggio 2028

Completamento dello studio (Stimato)

10 agosto 2028

Date di iscrizione allo studio

Primo inviato

13 ottobre 2026

Primo inviato che soddisfa i criteri di controllo qualità

28 ottobre 2026

Primo Inserito (Effettivo)

4 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

4 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

28 ottobre 2026

Ultimo verificato

1 ottobre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • FXS6837-PNH-302

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

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 .