META 10-19 in Patients With Relapsed/Refractory Autoimmune Hemolytic Anemia
Phase I Clinical Study on the Safety and Tolerability of META 10-19 Infusion in Patients With Relapsed/Refractory Autoimmune Hemolytic Anemia
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
This is a Phase I clinical study evaluating metabolically armed autologous CD19 CAR T-cell therapy (META 10-19) in patients with relapsed/refractory autoimmune hemolytic anemia (AIHA). The main purpose of this study is to assess the safety and tolerability of this therapy in patients with relapsed/refractory AIHA.
-Primary Objective: To evaluate the safety and tolerability of metabolically armed autologous CD19 CAR T-cell therapy (META 10-19) in patients with relapsed/refractory autoimmune hemolytic anemia (AIHA).
-Secondary Objectives:
- To evaluate the preliminary efficacy of metabolically armed autologous CD19 CAR T-cell therapy (META 10-19) in study participants with relapsed/refractory AIHA.
- To assess the pharmacokinetic (PK) and pharmacodynamic (PD) characteristics of the metabolically armed autologous CD19 CAR T-cell therapy (META 10-19).
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- 初期フェーズ 1
連絡先と場所
研究連絡先
研究連絡先
- 名前:RuoNan Li
- 電話番号:86+18810169952
- メール:liruonan@ihcams.ac.cn
研究場所
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-
Tianjin Municipality
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Tianjin、Tianjin Municipality、中国、300000
- Blood Diseases Hospital, Chinese Academy of Medical Sciences
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主任研究者:
- Jun Shi
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コンタクト:
- RuoNan Li
- 電話番号:86+18810169952
- メール:liruonan@ihcams.ac.cn
-
副調査官:
- Ruonan Li
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-
参加基準
適格基準
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
説明
Inclusion Criteria:
- Aged 18 to 75 years, regardless of genders.
- Diagnosis of AIHA (including warm antibody type, mixed warm and cold antibody type, cold agglutinin disease) or Evans syndrome, consistent with the Chinese Expert Consensus on the Diagnosis and Treatment of Autoimmune Hemolytic Anemia (2023), or the Diagnosis and Treatment of Autoimmune Hemolytic Anemia in Adults: Recommendations from the First International Consensus Meeting (Blood Rev, 2020), or the Chinese Expert Consensus on the Diagnosis and Treatment of Evans Syndrome (2024 Edition).
Definition of relapsed/refractory disease, meeting all of the following criteria:
- Hemoglobin < 10 g/dL with clinical manifestations of hemolytic anemia;
- After treatment with at least two immunosuppressive agents (which must include an anti-CD20 monoclonal antibody, with a cumulative dose of the anti-CD20 antibody reaching at least 375 mg/m² × 4, or a total dose of 2.0 g, or at least 6 cumulative administrations with an interval of ≥1 week between each);
- Glucocorticoid therapy for no less than 3 months (except for those with comorbidities that contraindicate corticosteroid use, severe infection, severe osteoporosis, previous fractures, or intolerance to glucocorticoids).
- Eastern Cooperative Oncology Group (ECOG) performance status score ≤ 2;
- Estimated life expectancy ≥12 weeks;
- Adequate organ function as assessed by laboratory tests: Serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3 × upper limit of normal (ULN); and minimal pulmonary reserve, defined as dyspnea ≤ grade 1 and oxygen saturation ≥ 93% while breathing room air; creatinine clearance (estimated by Cockcroft-Gault) ≥ 45 mL/min; cardiac ejection fraction ≥ 50%, with no signs of pericardial effusion on echocardiography (ECHO) and no clinically significant electrocardiogram (ECG) abnormalities.
- During the study period (from the signing of this informed consent form until at least 12 months after META 10-19 infusion, and until two consecutive PCR tests show no detectable CAR-T cells in the body), the study participant and their spouse/partner must use appropriate and effective contraceptive measures (excluding rhythm method/calendar-based contraception).
- Study participants must sign a written informed consent form approved by the Ethics Committee prior to the initiation of any screening procedures.
Exclusion Criteria:
- Previously diagnosed definite lymphoproliferative neoplasms; other malignant tumors within the past 5 years (excluding cured basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, breast carcinoma in situ, and cervical carcinoma in situ).
- Secondary AIHA caused by drugs or infection.
Presence of active hepatitis or a history of severe liver disease or condition during the screening period:
- Hepatitis B: HBsAg or HBeAg positive; or hepatitis B e antibody (HBe-Ab) and/or hepatitis B core antibody (HBc-Ab) positive with HBV-DNA copy number above the lower limit of detection.
- Hepatitis C: Anti-HCV positive and HCV RNA ≥ lower limit of quantification (LLoQ).
- Human immunodeficiency virus (HIV) antibody positive.
- Active syphilis infection (excluding those with only positive syphilis-specific antibodies).
- Previous history of organ transplantation or hematopoietic stem cell transplantation.
Severe cardiovascular diseases:
- Cardiovascular disease with New York Heart Association (NYHA) class > 2 within 6 months prior to the first study drug administration.
- Unstable angina or severe arrhythmia requiring medication, including QTcF > 480 ms (calculated by Fridericia's formula).
- Other significant electrocardiogram (ECG) abnormalities, including second-degree type II atrioventricular block, third-degree atrioventricular block, bradycardia (ventricular rate < 50 bpm with clinical symptoms), etc.
- Myocardial infarction within the past 6 months.
- Other cardiac diseases considered unsuitable for enrollment by the investigator.
- Undergone major surgery within the past 4 weeks that is deemed by the investigator as unsuitable for enrollment.
- Presence of active infection (e.g., sepsis, bacteremia, fungemia, uncontrolled pulmonary infection, active tuberculosis, etc.); active infection requiring intravenous anti-infective therapy within 7 days prior to screening.
- Receipt of CAR T-cell therapy within 6 months prior to screening, or positivity for ADA, or positivity for HAMA, or receipt of in vivo CAR T-cell therapy within the previous 6 months; or a history of severe immediate hypersensitivity reaction to any cellular product, excipients, or related drugs used in this study.
- Individuals with a history of epilepsy or other active central nervous system diseases (including but not limited to cerebrovascular accident, cerebral hemorrhage, cerebral infarction, severe traumatic brain injury, dementia, organic brain syndrome, etc.).
- Women with a positive pregnancy test or who are breastfeeding; women of childbearing potential and all male study participants who are unwilling or unable to use effective contraceptive methods during the study period and for at least 12 months after study drug infusion.
- Any other condition or circumstance that, in the investigator's opinion, would make the participant unsuitable for participation in this study.
研究計画
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)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
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実験的:META 10-19 CAR T-Cell Therapy
Participants will receive META 10-19 CAR T-cell infusion.
Participants will be closely monitored for 24 hours after infusion.
Hospitalization for a minimum of 14 days after infusion is recommended.
The duration of hospitalization and observation will be determined based on the investigator's clinical assessment of the participant's condition.
|
Metabolically Armed Autologous CD19 CAR T-cells.
Each subject receive metabolically autologous armed CD19 CAR T-cells by intravenous infusion.
他の名前:
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この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Incidence and severity of adverse events
時間枠:Up to 28 days after META 10-19 infusion.
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Assessed by CTCAE Version 6.0.
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Up to 28 days after META 10-19 infusion.
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二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Proportion of patients achieving response
時間枠:On Day 28 and at Months 2, 3, and 6 after META 10-19 infusion.
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Response is assessed based on hemoglobin (Hb), laboratory markers of hemolysis (serum bilirubin and lactate dehydrogenase), and transfusion requirements.
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On Day 28 and at Months 2, 3, and 6 after META 10-19 infusion.
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The maximum concentration (Cmax)
時間枠:Up to 6 months after META 10-19 infusion.
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The Cmax of CAR-T cell expansion in peripheral blood.
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Up to 6 months after META 10-19 infusion.
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Time to Peak (Tmax)
時間枠:Up to 6 months after META 10-19 infusion.
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The time to reach the maximum concentration (Tmax).
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Up to 6 months after META 10-19 infusion.
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AUC(0-day 28)
時間枠:Up to 28 days after META 10-19 infusion.
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AUC(0- day28) refers to the area under curve of CAR T-cell expansion between infusion and day 28 post infusion.
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Up to 28 days after META 10-19 infusion.
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Pharmacodynamics
時間枠:Up to 6 months after META 10-19 infusion.
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Pharmacodynamic effects will be assessed by changes in B-cell levels in peripheral blood and bone marrow, including percentage and absolute counts of B cells and plasma cells at different time points after infusion.
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Up to 6 months after META 10-19 infusion.
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協力者と研究者
協力者
協力者
研究記録日
主要日程の研究
研究開始 (推定)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
その他の研究ID番号
- LM-MATE10-19-19
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
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