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An Efficacy Study of XTMAB-16 in Patients With Pulmonary Sarcoidosis With or Without Extrapulmonary Manifestations

2026年8月26日 更新者:Xentria, Inc.
A study of XTMAB-16 in patients with pulmonary sarcoidosis

調査の概要

状態

まだ募集していません

詳細な説明

An Efficacy Study of XTMAB-16 in Patients With Pulmonary Sarcoidosis With or Without Extrapulmonary Manifestations

研究の種類

介入

入学 (推定)

182

段階

  • フェーズ2

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

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. Participant between 18 and 80 years (inclusive) of age.
  2. Weighs between 45 and 160 kg (99 to 353 lbs) at Screening.
  3. Diagnosis of pulmonary sarcoidosis (at least 6 months before Screening) using the 2020 American Thoracic Society (ATS) Clinical Practice Guideline (Crouser et al, 2020), the European Respiratory Society (ERS) or the World Association of Sarcoidosis and Other Granulomatous Disorders (WASOG) criteria including a compatible clinical and radiologic presentation with other causes of granulomatous disease ruled out (cutaneous and ocular involvement permitted).
  4. mMRC Dyspnea Scale of ≥1.
  5. Baseline pre-BD ppFVC of ≥ 50% during screening window, and confirmed at the Baseline visit prior to enrollment and dosing.
  6. Receiving corticosteroid treatment 5 to 25 mg/day of oral prednisone, or equivalent), during the screening period and, at the determination of the Investigator, is capable of undergoing the protocol specific corticosteroid taper regimen.
  7. Receiving treatment with methotrexate, azathioprine, mycophenolate, leflunomide, chloroquine, or hydroxychloroquine for at least 3 months before Screening that has been at a stable dose for 4 weeks before Screening. All efforts should be made to maintain stable background therapy at the Screening dose through the intervention period at the Investigator's discretion.
  8. Radiographic evidence of disease in the lung parenchyma (at least Scadding stage II disease) without the presence of significant fibrosis.

    Note: Significant fibrotic disease is defined as fibrosis > 20% as determined by central read.

  9. Able to provide written informed consent.
  10. In the opinion of the Investigator, the participant is capable of understanding and complying with protocol requirements.

Exclusion Criteria:

  1. Pregnant or breastfeeding women or women who are planning to become pregnant during the study.
  2. Known potentially significant fibrotic disease and/or active inflammation contained solely in the hilar region as shown by HRCT, confirmed by a central reader. Participants with current active inflammation in the hilar region with concurrent inflammation outside the hilar region may be included. A historical HRCT performed within 6 months of screening may be submitted for diagnostic confirmation by central review. If a participant's last HRCT was from >6 months of screening, an HRCT should be performed during screening for diagnostic confirmation by central review. Note: Significant fibrotic disease is defined as >20% fibrosis on HRCT.
  3. Clinically significant extra-pulmonary sarcoidosis requiring systemic therapy as determined by the Investigator.
  4. Any therapy with an anti-TNFα monoclonal antibody (e.g., infliximab, adalimumab, golimumab and their biosimilars) within 6 months.
  5. Baseline pre-BD ppFVC of >85%.
  6. Prior treatment with rituximab or repository corticotropin injection within the previous 12 months.
  7. Clinically significant CNS sarcoidosis requiring therapy, except history of isolated seventh cranial nerve palsy or evidence of demyelinating neurologic disease.
  8. Advanced congestive heart failure (New York Heart Association 3 or 4).
  9. Current disease presentation consistent with Lofgren's syndrome (i.e., presence of the triad of erythema nodosum, bilateral hilar lymphadenopathy on chest X-ray, and joint pain).
  10. Clinically significant pulmonary hypertension requiring treatment. Note: Clinically significant pulmonary hypertension requiring treatment would be defined as treatment with, i.e., prostacyclins, phosphodiesterase 5 inhibitors, and endothelin receptor antagonists.
  11. Known hypersensitivity to any component of the formulation of XTMAB-16.
  12. Evidence of active or latent tuberculosis (TB) by interferon-gamma release assay (IGRA) or invasive fungal infections at Screening.
  13. Known positive history of malignancy other than non-melanomatous skin cancer in the last 2 years, including in-situ carcinoma of the uterine cervix completely cured by radical surgery.
  14. Positive test result for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, coronavirus disease (COVID-19), TB, or a known history of human immunodeficiency virus (HIV) infection at Screening.
  15. Women of childbearing potential who are sexually active with a non-sterilized male partner and are not willing to adhere to highly effective birth control measures from the time of signing the informed consent, throughout the duration of the study, and for 90 days after 5 half-lives have elapsed since the last dose of study drug. See Appendix 4 for details on contraception requirements during the study.
  16. Male participants who are non-sterilized and sexually active with a female partner of childbearing potential and are not willing to use highly effective contraception from the time of signing the informed consent throughout the duration of the study, and for 90 days after 5 half-lives have elapsed since last dose of study drug. See Appendix 4 for details on contraception requirements during the study.
  17. Clinically significant hepatic or renal disease, including uncontrolled diabetes at the discretion of the Investigator.
  18. Any severe prior reaction to any type of biologics or human blood product such as albumin, immunoglobulin G (IgG), etc.
  19. Concurrent emphysema.
  20. Known hypercalcemia due to non-sarcoidosis conditions such as untreated hyperparathyroidism, at the discretion of the Investigator.
  21. Abnormal electrocardiogram (ECG): ventricular arrhythmias (non-sustained ventricular tachycardia (VT), multifocal or frequent premature ventricular contractions, bundle branch block, axis deviation, or abnormal Q waves). In the case of a corrected QT interval by Fredericia interval >450 ms (men) or >480 ms (women; participants with bundle branch block) or PR interval outside the range of 120 to 220 ms, the assessment may be repeated once for eligibility determination at Screening or Baseline.
  22. Donation or loss of 450 mL or more of his or her blood volume (including plasmapheresis) or transfusion of any blood product within 90 days prior to dosing.
  23. Known uncontrolled hypertension. Note: Uncontrolled hypertension is noted as blood pressure (BP) ≥160/100 mmHg despite antihypertensive therapy within 3 months of randomization.
  24. Clinical signs and symptoms consistent with COVID-19, e.g., fever, dry cough, dyspnea, sore throat, fatigue, new smell or taste disorder or confirmed infection by appropriate laboratory test within the last 4 weeks prior to Screening.
  25. In the opinion of the Investigator, inability to tolerate corticosteroid taper.
  26. Concurrent systemic steroid use for non-sarcoidosis conditions.
  27. Concurrent known auto-immune disease requiring treatment.
  28. Participation in another clinical trial of an investigational agent within 3 months (small molecule) / 6 months (biologics) or 5 half-lives (if known) of the agent, whichever is longer.
  29. Any condition that required hospitalization within the 3 months prior to Day 1 or is likely to require so during the study.
  30. Clinically significant abnormalities in the Screening physical exam, medical history, vital signs, ECG, or clinical laboratory tests that are not known to be due to concurrent sarcoidosis, and in the opinion of the Investigator and Medical Monitor should preclude the participant's participation in the clinical study.

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:ランダム化
  • 介入モデル:並列代入
  • マスキング:ダブル

武器と介入

参加者グループ / アーム
介入・治療
実験的:XTMAB-16 4 mg/kg Q2W for 3 doses, then Q4W IV up to 52 weeks
Infusion
プラセボコンパレーター:Placebo 4 mg/kg Q2W for 3 doses, then Q4W IV up to 52 weeks
輸液

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
メジャーの説明
時間枠
Absolute change from baseline in forced vital capacity (FVC) (mL) at Week 24
時間枠:Baseline to Week 24
To establish efficacy of XTMAB-16 as measured by FVC (mL) in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations(mL) in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 24

二次結果の測定

結果測定
メジャーの説明
時間枠
Absolute change from baseline in forced vital capacity (FVC) (mL) at Week 52
時間枠:Baseline to Week 52
To further establish efficacy of XTMAB-16 as measured by disease control in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 52
Quality of Life King's Sarcoidosis Questionnaire-Lung (KSQ-L) mean change
時間枠:Baseline to Week 24 and 52
To further establish efficacy of XTMAB-16 as measured by quality of life in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 24 and 52
Proportion of participants experiencing no independently adjudicated worsening (exacerbation) events through Week 52
時間枠:Baseline to Week 52
To further establish efficacy of XTMAB-16 as measured by disease control in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 52
King's Sarcoidosis Questionnaire - General (KSQ-G)
時間枠:Baseline to Week 24 and 52
To further establish efficacy of XTMAB-16 as measured by quality of life in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 24 and 52
Modified Medical Research Council (mMRC) Dyspnea Scale
時間枠:Baseline to Week 24 and 52
To further establish efficacy of XTMAB-16 as measured by quality of life in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 24 and 52
Fatigue Assessment Scale (FAS)
時間枠:Baseline to Week 24 and 52
To further establish efficacy of XTMAB-16 as measured by quality of life in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 24 and 52
Time to first adjudicated worsening (exacerbation) event through Week 52
時間枠:Baseline to Week 52
To further establish efficacy of XTMAB-16 as measured by disease control in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 52
Annualized worsening-event rate
時間枠:Baseline to Week 52
To further establish efficacy of XTMAB-16 as measured by disease control in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 52
Mean number of worsening events per participant
時間枠:Baseline to Week 52
To further establish efficacy of XTMAB-16 as measured by disease control in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 52
Imaging Endpoints High-resolution computed tomography (HRCT; 'worse,' 'no change,' or 'better')
時間枠:Baseline to Week 24 and 52
To further establish efficacy of XTMAB-16 as measured by imaging in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 24 and 52
Maximum observed concentration (Cmax)
時間枠:Baseline to Week 52
To characterize the Pharmacokinetics (PK) of XTMAB-16 in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 52
Clearence
時間枠:Baseline to Week 52
To characterize the Pharmacokinetics (PK) of XTMAB-16 in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 52
Volume Parameters
時間枠:Baseline to Week 52
To characterize the Pharmacokinetics (PK) of XTMAB-16 in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 52
Soluble tumor necrosis factor alpha (sTNFα)
時間枠:Baseline to Week 12, 24 and 52
To characterize the Pharmacodynamics (PD) of XTMAB-16 in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 12, 24 and 52
Interleukin-1beta (IL-1β)
時間枠:Baseline to Week 12, 24 and 52
To characterize the Pharmacodynamics (PD) of XTMAB-16 in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 12, 24 and 52
Soluble IL-2 receptor (sIL-2R)
時間枠:Baseline to Week 12, 24 and 52
To characterize the Pharmacodynamics (PD) of XTMAB-16 in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 12, 24 and 52
Number and percentage of participants who test positive for anti-drug antibody (ADA) at Baseline and transient and persistent positive status at Weeks 12, 24, and 52.
時間枠:Baseline to Week 12, 24 and 52
To characterize the immunogenicity of XTMAB-16 in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 12, 24 and 52
Number and percentage of participants who test positive for neutralizing antibody (nAb) at Baseline and transient and persistent positive status at Weeks 12, 24, and 52.
時間枠:Baseline to Week 12, 24 and 52
To characterize the immunogenicity of XTMAB-16 in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 12, 24 and 52
Adverse event (AE) assessments
時間枠:Baseline to Week 52
To evaluate continued safety and tolerability of XTMAB-16 in participants with pulmonary sarcoidosis with or without extrapulmonary manifestations
Baseline to Week 52

協力者と研究者

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スポンサー

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)

2026年10月30日

一次修了 (推定)

2029年10月31日

研究の完了 (推定)

2029年10月31日

試験登録日

最初に提出

2026年6月25日

QC基準を満たした最初の提出物

2026年6月25日

最初の投稿 (実際)

2026年7月2日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月31日

QC基準を満たした最後の更新が送信されました

2026年8月26日

最終確認日

2026年8月1日

詳しくは

本研究に関する用語

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

はい

米国FDA規制機器製品の研究

いいえ

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