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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.

調査の概要

状態

まだ募集していません

条件

介入・治療

詳細な説明

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.

研究の種類

介入

入学 (推定)

20

段階

  • フェーズ 3

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

      • Tianjin、中国
        • TianJin Medical University General Hospital
        • コンタクト:
    • Zhejiang
      • Hangzhou、Zhejiang、中国
        • First Affiliated Hospital of Zhejiang University
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:FXS6837

100 mg FXS6837 capsule

FXS6837 capsule will be taken orally for 24 weeks

この研究は何を測定していますか?

主要な結果の測定

結果測定
時間枠
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)
時間枠:24 weeks from Baseline (Week 18 through Week 24)
24 weeks from Baseline (Week 18 through Week 24)

二次結果の測定

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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Rong Fu, Doctor、Tianjin Medical University General Hospital
  • 主任研究者:Hongyan Tong、First Affiliated Hospital of Zhejiang University

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2027年1月26日

一次修了 (推定)

2028年5月17日

研究の完了 (推定)

2028年8月10日

試験登録日

最初に提出

2026年10月13日

QC基準を満たした最初の提出物

2026年10月28日

最初の投稿 (実際)

2026年11月4日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月4日

QC基準を満たした最後の更新が送信されました

2026年10月28日

最終確認日

2026年10月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • FXS6837-PNH-302

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。