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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.

Descripción general del estudio

Estado

Aún no reclutando

Intervención / Tratamiento

Descripción detallada

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 de estudio

Intervencionista

Inscripción (Estimado)

20

Fase

  • Fase 3

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Copia de seguridad de contactos de estudio

  • Nombre: Hui Liu
  • Número de teléfono: +86 13821113189
  • Correo electrónico: liuhui8003@qq.com

Ubicaciones de estudio

      • Tianjin, Porcelana
        • TianJin Medical University General Hospital
        • Contacto:
          • Hui Liu
          • Número de teléfono: +86 13821113189
          • Correo electrónico: liuhui8003@qq.com
    • Zhejiang
      • Hangzhou, Zhejiang, Porcelana
        • First Affiliated Hospital of Zhejiang University
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: FXS6837

100 mg FXS6837 capsule

FXS6837 capsule will be taken orally for 24 weeks

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
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)
Periodo de tiempo: 24 weeks from Baseline (Week 18 through Week 24)
24 weeks from Baseline (Week 18 through Week 24)

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
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)
Periodo de tiempo: 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
Periodo de tiempo: Week2 to Week24
Week2 to Week24
Change from baseline in Hb as mean of visits between Week18 and Week24
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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;
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: up to 24 weeks
up to 24 weeks
Incidence of MAVEs between Week1 and Week24
Periodo de tiempo: up to 24 weeks
up to 24 weeks
Safety evaluation: All participants will be observed for any adverse event (AE) during the clinical study.
Periodo de tiempo: up to 24 weeks
up to 24 weeks
Population Pharmacokinetics (PK): Maximum Observed Concentration (Cmax) of FXS6837
Periodo de tiempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24
Population Pharmacokinetics (PK): Plasma trough concentration (Ctrough) of FXS6837
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: From pre-dose on Day1 to Week24
From pre-dose on Day1 to Week24

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

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

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

26 de enero de 2027

Finalización primaria (Estimado)

17 de mayo de 2028

Finalización del estudio (Estimado)

10 de agosto de 2028

Fechas de registro del estudio

Enviado por primera vez

13 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

28 de octubre de 2026

Publicado por primera vez (Actual)

4 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

4 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

28 de octubre de 2026

Última verificación

1 de octubre de 2026

Más información

Términos relacionados con este estudio

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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