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Sirolimus Pre-conditioning on T Cell Activity and T-cell Engaging Bispecific Antibody Efficacy in Multiple Myeloma

2026年6月2日 更新者:Christopher Strouse

Impact of Sirolimus Pre-conditioning on T Cell Activity and T-cell Engaging Bispecific Antibody Efficacy in Multiple Myeloma

This is a single center, single arm Phase Ib study with expansion cohort designed to establish the safety and physiologic effects of sirolimus pre-conditioning followed by T-cell engaging bispecific antibody therapy.

調査の概要

詳細な説明

This is a Phase Ib trial with expansion cohort to assess the safety and estimate the preliminary efficacy of sirolimus pre-conditioning prior to treatment with a T-cell engaging bispecific antibody in patients with relapsed / refractory multiple myeloma previously exposed to T-cell engager therapy. Following Phase Ib, the study will enroll an expansion cohort to test the hypothesis that sirolimus pre-conditioning will result in an increase in the Teffector: Texhausted -cell ratio.

研究の種類

介入

入学 (推定)

10

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

研究場所

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:

To be eligible to participate in this study, an individual must meet all of the following criteria:

  • Willingness and ability to provide signed and dated informed consent form.
  • Stated willingness to comply with all study procedures and availability for the duration of the study.
  • Aged 18 years of older.
  • Diagnosis with multiple myeloma, per IMWG Consensus Criteria.20
  • Planned for treatment with teclistamab, or talquetamab per standard of care, label indications.15
  • Prior exposure to any of the following types of T-cell engaging therapies.

    1. Anti-BCMA x CD3 bispecific antibody (for example: teclistamab, elranatamab)
    2. Anti-GPRC5d x CD3 bispecific antibody (for example: talquetamab)
    3. Anti-GPRC5d x CD3 x CD38 trispecific antibody
    4. Anti-BCMA x CD3 x CD38 trispecific antibody
    5. Anti-BCMA x CD3 x GPRC5d trispecific antibody
    6. Anti-BCMA chimeric antigen T-cell (for example: idecabtagene vicleucel, ciltacabtagene autoleucel)
    7. Anti-FcRL5 x CD3 bispecific antibody
  • Required clinical laboratory values during screening phase

Hematologic Parameters Hemoglobin ≥7.0 g/dL; Platelets ≥25 x 109/L; Absolute Lymphocyte Count ≥0.2 x 109/L

Chemistries AST/ALT < 5 x the ULN; Total Bilirubin < 3 x the ULN

  • Ability to take oral medication and be willing to adhere to the sirolimus pre-conditioning regimen.
  • ECOG performance status of 0, 1, or 2 (KPS of >50).
  • For males of reproductive potential: use of condoms or other methods to ensure effective contraception with partner per section5.3.
  • Agreement to adhere to Lifestyle Considerations (see section 5.3) throughout study duration.

Exclusion Criteria:

An individual who meets any of the following criteria will be excluded from participation in this study:

  • Participants whose multiple myeloma is progressing at a rapid pace requiring immediate anti-myeloma therapy per assessment by the principal investigator or enrolling investigator are excluded.
  • Excluded concomitant medication exposures:

    • Exposure to corticosteroids within 1 week of treatment start
    • Exposure to calcineurin inhibitor or mTOR inhibitors (tacrolimus, everolimus, temsirolimus, sirolimus)
    • Immunomodulatory monoclonal antibodies targeting tumor necrosis factor alpha (e.g. infliximab), interleukin 6 (e.g. siltuximab),
    • Janus kinase inhibitors (e.g. ruxolitinib)
    • Any other investigational drug within 28 days
  • History of allogeneic hematopoietic cell transplantation.
  • Excluded concurrent medical conditions:

    • Active uncontrolled infection within 7 days prior to treatment start
    • Uncontrolled thrombotic event within 3 months of treatment start
    • Acute myocardial infarction or acute coronary syndrome within 6 months of start of treatment
    • Uncontrolled inflammatory bowel disease
    • Active hepatitis B virus, hepatitis C virus, or Human Immunodeficiency Virus infection
    • Uncontrolled rheumatologic conditions
    • Use of ACE-inhibitor therapy within 1 week of treatment start

      • Patients found to be taking ace-inhibitor therapy during screening can be included if the ace-inhibitor is substituted for an angiotensin receptor blocking agent. (https://drug-interactions.medicine.iu.edu/main-table)
      • CYP3A4/p-gp inhibitors and inducers for 7 days prior to sirolimus doses and 7 days after sirolimus doses(see appendix A for list)
    • Any other current active malignancy or history of metastatic malignancy that has the potential to interfere with the safety or efficacy assessment of the investigational intervention
  • Pregnancy or lactation.
  • Known allergic reactions to study agent (sirolimus).

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:Sirolimus in combination with teclistamab or talquetamab
This study is designed to test changes in immune cell populations of patients with multiple myeloma exposed to short pre-conditioning with sirolimus prior to teclistamab or talquetamab. Safety of the combination will also be assessed.
Sirolimus is an immunosuppressant drug. Sirolimus binds to FK binding protein 12 and inhibits mTOR. This then suppresses T-cell proliferation and inhibits progression from G1 to S phase of the cell cycle.
他の名前:
  • ラパマイシン
Teclistamab is a bispecific antibody that binds the CD3 receptor on T-cells and the B-cell maturation antigen on multiple myeloma cells and healthy B-lineage cells.
他の名前:
  • テクヴァイリ
Talquetamab is a bispecific antibody that binds the CD3 receptor on T-cells and the GPRC5d receptor on multiple myeloma cells.
他の名前:
  • タルヴィー

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
Phase Ib: Dose limiting toxicities (DLTs) as measured by NCI Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
時間枠:From treatment initiation through 30 days post last dose of study treatment
The incidence of treatment-emergent adverse events will be summarized by system organ class and/or preferred term, type of adverse event, severity (based on NCI CTCAE v5.0) grades), and relation to study treatment. The most severe grade per participant will be reported. Adverse events leading to premature discontinuation from the study intervention and serious treatment-emergent adverse events will be presented in tabular form.
From treatment initiation through 30 days post last dose of study treatment
Expansion Cohort: Participants change in the Teffector: Texhausted cell ratio
時間枠:From treatment initiation through 3 months
Testing the null hypothesis H0: ΔPost-Pre = 0 versus the alternative H1: ΔPost-Pre ≠ 0. Results will be used as preliminary estimates to inform a subsequent larger trial.
From treatment initiation through 3 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Participant change in the following T-cell subsets: T-regulatory; T-Effector Memory (T-EM); T-Effector Memory expressing RA (T-EMRA)
時間枠:From treatment initiation through 3 months
The within participant change in the following T-cell subsets will be estimated: T-regulatory, T-EM, T-EMRA. Mixed effects regression models will be utilized to estimate changes. Random effects will be included to account for the longitudinally correlated nature of repeated measurements. Graphical plots of the estimated mean and associated 95% confidence intervals by time point in the study will be produced.
From treatment initiation through 3 months
The proportion of participants with grade 3 or higher CRS
時間枠:From treatment initiation through 3 months
The rate of grade ≥3 CRS will be defined as the proportion of participants who develop grade 3 or higher CRS. The rate of grade ≥3 CRS will be reported as a binomial proportion along with a two-sided 95% confidence interval.
From treatment initiation through 3 months
The proportion of participants with grade 3 or highter ICANS
時間枠:From treatment initiation through 3 months
The rate of grade ≥3 ICAN will be defined as the proportion of participants who develop grade 3 or higher ICAN. The rate of grade ≥3 ICAN will be reported as a binomial proportion along with a two-sided 95% confidence interval.
From treatment initiation through 3 months
The proportion of participants with a very good partial response (VGPR) or better at 3 months
時間枠:Three months after the initiation of treatment
The 3-month response rate will be defined as the proportion of participants with a very good partial response (VGPR) or better at 3 months. The 3-month response rate will be reported as a binomial proportion along with a two-sided 95% confidence interval.
Three months after the initiation of treatment

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:Christopher Strouse, MD、University of Iowa

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6月1日

一次修了 (推定)

2029年6月1日

研究の完了 (推定)

2029年10月1日

試験登録日

最初に提出

2026年5月5日

QC基準を満たした最初の提出物

2026年5月5日

最初の投稿 (実際)

2026年5月12日

学習記録の更新

投稿された最後の更新 (実際)

2026年6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6月2日

最終確認日

2026年6月1日

詳しくは

本研究に関する用語

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?

いいえ

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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