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再発/難治性急性骨髄性白血病患者におけるC6セラミドナノリポソーム(CNL)の研究 (KNAN2001)

2026年11月1日 更新者:Keystone Nano, Inc

再発/難治性急性骨髄性白血病(RR-AML)患者におけるC6セラミドナノリポソーム(CNL)の第I相試験

The study objective is to evaluate patient safety for patients with refractory and relapsed AML being treated with Ceramide NanoLiposome (CNL) .

調査の概要

状態

募集

条件

介入・治療

詳細な説明

The research team has shown that C6 ceramide nanoliposome (CNL) has anti-cancer activity in laboratory models of AML and that when it is combined with other cancer-fighting drugs, it works better.

The primary goal of this study is to evaluate the safety of CNL given without other cancer treatments in patients with AML where either their initial treatment didn't work or it stopped working and the AML came back (refractory or relapsed AML, aka RR-AML). This study seeks to determine the right dose to start with in later studies when CNL is combined with other drugs in potential future studies.

CNL is given by intravenous (IV) infusion and will be given twice a week in this study. Participants will receive study treatment as long as it is considered safe for them to continue, though their disease status will be checked regularly to make sure that their disease has not gotten worse. Blood samples will be collected at many time-points to see how their bodies are responding to the drug and how long it stays in the blood.

The first patients in the study will start at one dose of the drug and, if that is shown to be safe, the next group will be treated at a slightly higher dose. Participants will be given CNL by intravenous (IV) infusion twice a week over about 2 hours and then they will be monitored for about 2 hours to make sure they don't have any bad side effects, but initially patients will be required to stay at the site for about 6 hours after the start of the infusion in order to get blood draws to see how long the drug stays active in their system.

Participants will have a bone marrow biopsy before their second "cycle" of drug (after about 1 month) and then again before their third cycle of drug in order to see how their disease is responding. After that, bone marrow biopsies will be about every other cycle based on what the study doctor recommends. If the doctor doesn't think that CNL is helping their disease, or if their doctor decides that it is not safe for them to continue, they will be taken off study treatment. Participants will be followed for safety and disease status for up to 6 months.

研究の種類

介入

入学 (推定)

15

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

研究連絡先のバックアップ

研究場所

    • Virginia
      • Charlottesville、Virginia、アメリカ、22903
        • 募集
        • University of Virginia Cancer Center
        • 主任研究者:
          • Michael Keng, MD
        • 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. Signed informed consent is obtained prior to conducting any study-specific screening procedures.

  2. Willing and able to understand the nature of this study and to comply with the study and follow-up procedures.

  3. Age and Disease: ≥ 18 years of age with refractory or relapsed AML

    Refractory AML: Patients who fail to achieve a complete remission (CR) or a complete remission with incomplete count recovery (CRi) after one or more ines of AML directed therapy.

    Relapsed AML: Patients who achieved a complete remission (CR) or a complete remission with incomplete count recovery (CRi) with one or more prior lines of AML directed therapy but then developed a relapse of AML.

    Note: Patients are eligible even if they have not received intensive induction chemotherapy but have been treated with other AML directed therapy like hypomethylating agents (azacitidine, decitabine).

  4. Eastern Cooperative Oncology Group (ECOG) performance status must be ≤2.

  5. ECOG performance status must be ≤2

  6. Peripheral white blood cell (WBC) count <30,000/µL. For cyto-reduction, the following are allowed to reduce WBC count to < 30,000/µL:

    • hydroxyurea is allowed during screening and through the end of Cycle,
    • cytarabine is allowed during screening but not after registration and should be limited 1 g/m2 or less from time of consent to registration.
  7. Adequate organ function as evidenced by the following laboratory findings:

    • Total bilirubin ≤ 1.5 × upper limit of normal (ULN) or < 3 x ULN for patients with Gilbert-Meulengracht Syndrome
    • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 × ULN if not attributed to leukemia, or ≤ 5 x ULN if attributed to leukemia
    • Creatinine clearance > 60 mL/min.

Exclusion Criteria:

Patients meeting any of the following criteria are ineligible for study entry:

  1. Uncontrolled intercurrent illness including, but not limited to, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmias not well controlled with medication, myocardial infarction within the previous 6 months before registration, or psychiatric illness/social situations that would limit compliance with study requirements.
  2. Patients may not be receiving any other concurrent investigational agents during study treatment and not for at least within one week prior to starting study treatment.
  3. Since the teratogenic potential of this combination is currently unknown, females who are pregnant or lactating are excluded.
  4. History of any other malignancies within the preceding 12 months before registration with the exception of in-situ cancer, non-muscle invasive bladder cancer, non-metastatic prostate cancer, basal or squamous cell skin cancer.
  5. Life-threatening illnesses other than AML, uncontrolled medical conditions or organ system dysfunction that, in the Investigator's opinion, could compromise the patient's safety or put the study outcomes at risk.
  6. Evidence of isolated extramedullary disease.
  7. Acute Promyelocytic Leukemia.
  8. AML with active central nervous system (CNS) involvement (as determined by study investigator).
  9. Severe infection requiring treatment that would interfere with study drug(s) or study participation in the opinion of the treating investigator.
  10. Past Hematopoietic stem cell transplant (HSCT) with graft vs host disease, immunosuppression other than low dose prednisone (10 mg) (or equivalent does of another immunosuppressant) within the 4 weeks before registration.
  11. All adverse reactions from prior therapy must have recovered to Grade ≤ 1 or acceptable baseline per treating 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:Open Label Administration of Ceramide NanoLiposome

Ceramide NanoLiposome will be administered by Intravenous Dosing twice per week in accordance with the protocol relative to dose escalation. There is no placebo group or arm of the study.

Ceramide NanoLiposome will be given by IV twice a week. The dose, which is based on body size, will be increased for the next group of patients if the first group of patients tolerates that dose and it will decrease for the next group if they do not tolerate the dose.

他の名前:
  • セラミドナノリポソーム

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
Number of Patients with Dose Limiting Toxicities as defined in Protocol Section 13.5
時間枠:At the end of the the first cycle of administration (each cycle is 28 days)

Dose Limiting Toxicities within the first cycle of CNL monotherapy. See section 13.5 of Protocol for the complete list of Dose Limiting Toxicities

At the end of the the first cycle of administration (each cycle is 28 days)
Number of Patients with Adverse Events
時間枠:Through study completion, an average of 24 weeks

Number of Patients with Adverse Events

Through study completion, an average of 24 weeks
Severity of Adverse Events
時間枠:Through study completion, an average of 24 weeks

Severity of Adverse Event As Described in Protocol

Through study completion, an average of 24 weeks
Duration of Adverse Events
時間枠:Length of Adverse Events as measured in days, measured through study completion, an average of 24 weeks

Duration of Adverse Events, As Described in Protocol, measured in days

Length of Adverse Events as measured in days, measured through study completion, an average of 24 weeks
Duration of therapy
時間枠:Through study completion, an average of 24 weeks

Duration of therapy provided as measured in days

Through study completion, an average of 24 weeks
Dose Levels achieved during study
時間枠:Through study completion, an average of 24 weeks

Dose levels administered in milligrams per m2

Through study completion, an average of 24 weeks
Concentration Max (C Max)
時間枠:Through cycle one, 28 days (each cycle is 28 days)

Maximum Serum Concentration measured, in nanograms/milliliter

Through cycle one, 28 days (each cycle is 28 days)
Time to Maximum Study Drug (T Max)
時間枠:Through cycle one, 28 days (each cycle is 28 days)

Time to maximum concentration measured, in minutes

Through cycle one, 28 days (each cycle is 28 days)
Half Life of Study Drug
時間枠:Through cycle one, 28 days (each cycle is 28 days)

Time for drug to be reduced to half of the starting concentration (in minutes)

Through cycle one, 28 days (each cycle is 28 days)
Study Drug Clearance
時間枠:Through cycle one, 28 days (each cycle is 28 days)

The Amount of Study Drug Cleared per unit time (Nanograms/Minute)

Through cycle one, 28 days (each cycle is 28 days)
Ratio of C16/C24 Ceramides
時間枠:After one cycle of therapy (Day 28)

Ratio of Ceramide 16 to Ceramide 24 (ng of C16/ng of C18) from bone marrow biopsy

After one cycle of therapy (Day 28)
Clinical Response - Complete Response
時間枠:After Cycle Two (56 days)

Complete Response

After Cycle Two (56 days)
Clinical Response - Complete Response with Incomplete Hematologic Recovery (CRi)
時間枠:After Cycle Two (56 days)

Complete Response with Incomplete Hematological Recovery as defined by blasts in bone marrow

After Cycle Two (56 days)
Clinical Response - Partial Remission
時間枠:After Cycle Two (56 days)

Partial Remission (as defined by blasts in bone marrow)

After Cycle Two (56 days)

二次結果の測定

結果測定
メジャーの説明
時間枠
Number of Patients with Grade 3 or 4 Adverse Events
時間枠:Through study completion, an average of 24 weeks

Grade 3 and 4 adverse events as defined by CTCAE v5.0

Through study completion, an average of 24 weeks
Overall Response
時間枠:Through study completion, an average of 24 weeks, and up to 24 weeks afterwards (total of 48 weeks)

Overall response of CNL monotherapy in patients with RR-AML: Complete remission (CR) + Complete remission with incomplete count recovery (CRi) + partial response (PR). CR, CRi and PR as defined as European LeukemiaNet 2017 (ELN 2017) response criteria

Through study completion, an average of 24 weeks, and up to 24 weeks afterwards (total of 48 weeks)
Event Free Survival
時間枠:From registration to 24 weeks after completion of experimental drug treatment

Event-free survival (EFS): the time from registration until documented refractory disease, relapse after achieving CR/CRi, or death from any cause, whichever is observed first

From registration to 24 weeks after completion of experimental drug treatment
Overall Survival
時間枠:From registration to 24 weeks following drug administration

Overall survival (OS)

From registration to 24 weeks following drug administration
Quality of Life according to EORTC Quality of Life Questionnaire (QLQ) C30
時間枠:Prior to starting study treatment, on day 1 of each cycle (each cycle is 28 days), and at end of treatment (which is expected to be 2 to 3 months (cycles) for most patients

Quality of life according to EORTC Quality of Life Questionnaire C30

Prior to starting study treatment, on day 1 of each cycle (each cycle is 28 days), and at end of treatment (which is expected to be 2 to 3 months (cycles) for most patients

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

協力者

捜査官

  • スタディディレクター:Daniel Vlock, MD、Keystone Nano, Inc
  • スタディチェア:Christopher Prior, Ph.D.、Keystone Nano

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

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)

2025年10月1日

一次修了 (推定)

2027年1月30日

研究の完了 (推定)

2027年2月28日

試験登録日

最初に提出

2020年11月30日

QC基準を満たした最初の提出物

2021年1月15日

最初の投稿 (実際)

2021年1月20日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月3日

QC基準を満たした最後の更新が送信されました

2026年11月1日

最終確認日

2026年11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

  • KNAN2001
  • 5R44CA275609-02 (米国 NIH グラント/契約)

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?

はい

IPD プランの説明

Likely to be shared with PO1 Researchers at UVA and Penn State. In addition to yearly FDA reports, anticipate potential manuscripts as well but not yet decided with all participants.

IPD 共有時間枠

Dec 1, 2026

IPD 共有アクセス基準

6 months after Trial

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

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

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。