Safety and Efficacy of KSVCBD Injection in Multiple Myeloma Expressing CD19 and/or BCMA
2026年9月13日 更新者:Han weidong、Chinese PLA General Hospital
A Multicenter Clinical Study on the Safety and Efficacy of KSVCBD Injection in the Treatment of Multiple Myeloma With Positive Expression of CD19 and/or BCMA
KSVCBD injection is an in vivo Chimeric Antigen Receptor T-Cell (CAR-T cell) therapy product.
This multicenter, single-arm, open-label, early exploratory clinical study is designed to evaluate the preliminary safety and efficacy of KSVCBD injection in patients with relapsed or refractory (r/r) multiple myeloma(MM) expressing CD19 and/or BCMA.
調査の概要
詳細な説明
A structurally modified, third-generation, self-inactivating lentiviral vector was used in KSVCBD injection.
This modified vector exhibits reduced immunogenicity and enables efficient T-cell targeting, thereby facilitating the in vivo generation of CD19/BCMA CAR T cells from endogenous T cells.
Simultaneously targeting BCMA to eliminate plasma cells producing anti-lentivirus and anti-CD19 scFv antibodies enables repeated infusion.
The safety and efficacy of CD19/BCMA dual-target autologous CAR-T therapy for the treatment of r/r MM have already been validated in clinical studies.
In this study, dose-escalation research will be conducted to explore the safety and preliminary efficacy of CD19/BCMA dual-target in vivo CAR-T therapy in patients with r/r MM who are positive for CD19 and/or BCMA expression.
研究の種類
介入
入学 (推定)
9
段階
- フェーズ 1
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
- 名前:Weidong Han, M.D.
- 電話番号:+86-010-55499341
- メール:hanwdrsw@sina.com
研究場所
-
-
-
Beijing、中国
- まだ募集していません
- Department of Hematology, Beijing Chao-Yang Hospital, Capital Medical University
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コンタクト:
- Wen Gao, M.D.
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Tianjin、中国
- まだ募集していません
- National Clinical Research Center for Blood Diseases, State Key Laboratory of Experimental Hematology, Blood Diseases Hospital & Institute of Hematology, Chinese Academy of Medical Sciences & Peking Union Medical College
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コンタクト:
- Lugui Qiu, M.D.
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副調査官:
- Gang An, M.D.
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Beijing Municipality
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Beijing、Beijing Municipality、中国、100853
- 募集
- Biotherapeutic Department of Chinese PLA General Hospital
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副調査官:
- Yang Liu, M.D.
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副調査官:
- Jinhong Shi, M.S.
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コンタクト:
- Weidong Han, M.D.
- 電話番号:+86-10-66937463
- メール:hanwdrsw@sina.com
-
-
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
Key Inclusion Criteria:
- Age 18-75 years (inclusive), any gender.
Subjects must meet the following diagnostic and treatment criteria:
2.1 According to the IMWG 2014 diagnostic criteria, subjects must have a confirmed diagnosis of multiple myeloma and be in a relapsed or refractory state at screening, while meeting all of the following conditions:
- Must have received at least 3 prior lines of MM therapy (including a proteasome inhibitor and an immunomodulatory agent). consecutive cycles of induction chemotherapy, hematopoietic stem cell transplantation, and maintenance therapy are considered as one line of therapy if no disease progression occurs between these treatments. each line of therapy must consist of at least one complete treatment cycle, unless the best response to that regimen was disease progression.
- Must have experienced disease progression during or within 12 months after the most recent anti-myeloma therapy. or the subject must have experienced disease progression within the last 6 months and subsequently shown no response to the most recent line of therapy. Lack of response is defined as failure to achieve at least a minimal response (MR) or experiencing disease progression (PD) during treatment.
2.2 Subjects judged by the investigator to be intolerant to standard therapy may also be included in the study.
Presence of measurable lesions at screening as determined by any of the following criteria:
- Serum monoclonal paraprotein (M-protein) level ≥ 1.0 g/dL, or urinary M-protein level ≥ 200 mg/24 hours. or
- For light chain multiple myeloma without measurable lesions in serum or urine: serum immunoglobulin free light chain level ≥ 10 mg/dL and an abnormal serum immunoglobulin κ/λ free light chain ratio.
- Positive expression of CD19 and/or BCMA in tumor tissue confirmed by flow cytometry and/or histopathology (previous pathology or flow cytometry diagnosis of CD19 and/or BCMA in the patient, as confirmed by the investigator, is acceptable). For subjects who have previously received anti-CD19 and/or anti-BCMA therapy, a tumor biopsy should be performed to confirm current positive expression of CD19 and/or BCMA.
- Toxicities from any prior therapy must be stable and have resolved to ≤ Grade 1 (excluding hematologic toxicities and clinically insignificant toxicities such as alopecia).
- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2.
Key Exclusion Criteria:
- Expected survival < 3 months.
- History of or concurrent active malignancy. Exceptions include: carcinoma in situ of the cervix that has been cured or with no recurrence for at least 3 years, non-invasive basal cell or squamous cell skin cancer, locally advanced prostate cancer that has received curative treatment, or ductal carcinoma in situ after radical surgery.
- Prior allogeneic hematopoietic stem cell transplantation (allo-HSCT) or autologous HSCT within 3 months prior to KSVCBD infusion.
- Diagnosis of plasma cell leukemia, Waldenström's macroglobulinemia, POEMS syndrome, or primary AL amyloidosis.
- Presence of CNS metastasis or symptoms of CNS metastasis.
- Receipt of anti-tumor therapy that is still within 5 half-lives prior to the planned KSVCBD infusion.
- Presence of uncontrolled active infections.
- Positive for human immunodeficiency virus (HIV) antibody, positive for Treponema pallidum antibody, positive for hepatitis B surface antigen (HBsAg) or positive for hepatitis B core antibody (HBcAb) with detectable peripheral blood HBV DNA, or positive for hepatitis C virus (HCV) antibody with detectable HCV RNA. except for infections that the investigator judges can be prevented or controlled with medication.
- Known active autoimmune disease requiring systemic treatment.
- Known severe allergy to the study drug or any of its components.
- Pregnant or breastfeeding women.
- Receipt of a live vaccine within 6 weeks prior to enrollment.
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:KSVCBD injection
Administered by IV infusion
|
KSVCBD injection is an in vivo CAR-T therapy targeting CD19/BCMA.
Three dose levels are predefined, and KSVCBD will be dose-escalated per the protocol-specified doses
|
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 |
|---|---|---|
|
Dose limited toxicity (DLT)
時間枠:Within 28 days post-infusion
|
DLT is defined as any of the following adverse events (AEs) related to KSVCBD infusion occurring within 28 days after KSVCBD infusion
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Within 28 days post-infusion
|
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Incidence and severity of adverse events of special interest (AESI)
時間枠:Within 24 months post-infusion
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AESI including grade ≥ 3 Cytokine Release Syndrome (CRS), Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS), and infections
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Within 24 months post-infusion
|
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Incidence and severity of AEs and serious adverse events (SAEs)
時間枠:Within 24 months post-infusion
|
AEs refer to any adverse medical events occurring in subjects from the initiation of KSVCBD administration during clinical trials.
SAEs denote events involving death, life-threatening conditions, significant disability/incapacity, hospitalization or prolonged hospitalization arising after KSVCBD administration in subjects.
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Within 24 months post-infusion
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
KSVCBD lentiviral particle concentration
時間枠:Within 24 months post-infusion
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KSVCBD lentiviral particle concentration in peripheral blood.
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Within 24 months post-infusion
|
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Number of CD19-positive cells
時間枠:Within 24 months post-infusion
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Number of CD19-positive cells in peripheral blood.
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Within 24 months post-infusion
|
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Duration of Response (DOR)
時間枠:Within 24 months post-infusion
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Time from first documented PR or better to relapse or disease progression, or death from any cause
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Within 24 months post-infusion
|
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Time to Response (TTR)
時間枠:Within 24 months post-infusion
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Time from administration to first documented PR or better.
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Within 24 months post-infusion
|
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Progression-Free Survival (PFS)
時間枠:Within 24 months post-infusion
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Time from administration to disease progression or death from any cause, whichever occurs first.
|
Within 24 months post-infusion
|
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Overall Survival (OS)
時間枠:Within 24 months post-infusion
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Time from administration to death from any cause.
|
Within 24 months post-infusion
|
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Number of CAR-positive T cells
時間枠:Within 24 months post-infusion
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Number of CAR-positive T cells in peripheral blood.
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Within 24 months post-infusion
|
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CAR gene copy number
時間枠:Within 24 months post-infusion
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CAR gene copy number in peripheral blood.
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Within 24 months post-infusion
|
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Number of BCMA-positive cells
時間枠:Within 24 months post-infusion
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Number of BCMA-positive cells in peripheral blood.
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Within 24 months post-infusion
|
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Objective Response Rate (ORR)
時間枠:Within 24 months post-infusion
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ORR includes Stringent Complete Remission (sCR), CR, Very Good Partial Remission (VGPR), and PR.
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Within 24 months post-infusion
|
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Minimal Residual Disease (MRD) negativity rate
時間枠:Within 24 months post-infusion
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Rate of achieving MRD negativity
|
Within 24 months post-infusion
|
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≥ CR rate
時間枠:Within 24 months post-infusion
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Rate of achieving ≥ CR (CR and sCR)
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Within 24 months post-infusion
|
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。
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 (実際)
2026年9月3日
一次修了 (推定)
2028年12月15日
研究の完了 (推定)
2029年3月15日
試験登録日
最初に提出
2026年5月27日
QC基準を満たした最初の提出物
2026年5月27日
最初の投稿 (実際)
2026年6月2日
学習記録の更新
投稿された最後の更新 (実際)
2026年9月15日
QC基準を満たした最後の更新が送信されました
2026年9月13日
最終確認日
2026年9月1日
詳しくは
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。