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Bioequivalence Study of Liposomal Doxorubicin 20 mg/10 mL (Doxopeg® vs Caelyx®) in Advanced Cancer Patients

2026年6月9日 更新者:Zodiac Produtos Farmaceuticos S.A.

Multicenter, Open Label, Balanced, Randomized, Two-Treatment, Two-Period, Two- Sequence, Single Dose, Crossover Bioequivalence Study Between Two Formulations of Doxorubicin Hydrochloride Liposome Injection 20 mg/10 mL (2 mg/mL) [Doxopeg® Manufactured by FAPASA - Farmaceutica Paraguay S.A. and Registered by Adium S.A., Formerly Zodiac Produtos Farmacêuticos S.A, (Test Formulation) and Caelyx® Manufactured by Janssen Pharmaceutica NV (Reference Formulation)] in Patients With Advanced Ovarian Cancer or Metastatic Breast Cancer

To characterize the pharmacokinetic profile of pegylated liposomal doxorubicin formulations, a multicenter, randomized, two-period crossover study was conducted in 74 patients with advanced ovarian cancer or metastatic breast cancer. Blood samples were collected up to 336 hours post-dose, and plasma concentrations of encapsulated and free doxorubicin were quantified using validated LC-MS/MS methods. Pharmacokinetic parameters (Cmax, AUC0-t, AUC0-inf, tmax, t1/2, Vd, and Cl) were calculated using noncompartmental analysis.

調査の概要

研究の種類

介入

入学 (実際)

74

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:

  1. Participant must sign an ICF indicating that the participant understands the purpose of, and procedures required for the study and is willing to participate in the study.
  2. Female participant must be 18 to 75 years of age (both inclusive), at the time of signing the informed consent.
  3. Participant meeting one of the following criteria:

    a Participant with documented advanced ovarian cancer whose disease has progressed or recurred after platinum-based chemotherapy AND who are already receiving or scheduled to start the monotherapy with liposomal doxorubicin (pegylated) at a dose of 50 mg/m2.

    b Participants with documented metastatic breast cancer AND who are already receiving or scheduled to start the monotherapy with liposomal doxorubicin (pegylated) at a dose of 50 mg/m2.

  4. Life expectancy of ≥12 weeks at screening visit.
  5. An Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1 or 2 at screening visit.
  6. Participant should have recovered from any toxic effects of previous chemotherapy as judged by the Investigator. Participants who are already receiving liposomal doxorubicin (pegylated) at a dose of 50 mg/m2.should not require dose reduction(s) in next planned cycle in the study due to toxicity
  7. A participant is eligible to participate if she is not pregnant or breastfeeding, and at least one of the following conditions applies:

    a Is not a woman of childbearing potential (WOCBP) b Is a WOCBP and using a contraceptive method that is highly effective (with a failure rate of <1% per year), with low user dependency when used consistently and correctly, during the intervention period and for at least eight months after the last dose of study intervention and agrees not to donate eggs (ova, oocytes) for the purpose of reproduction during the study and for at least eight months after the last dose of study intervention. The investigator should evaluate the effectiveness and the potential for contraceptive method failure (eg, noncompliance, recently initiated) of the contraceptive method in relationship to the first dose of study intervention.

    • A WOCBP must have a negative highly sensitive serum pregnancy test at screening; and urine pregnancy test within 24 hours before the first dose of study intervention.
    • If a urine test cannot be confirmed as negative (e.g., an ambiguous result), a serum pregnancy test is required. In such cases, the participant must be excluded from participation if the serum pregnancy result is positive.

    The investigator is responsible for review of medical history, menstrual history, and recent sexual activity to decrease the risk for inclusion of a woman with an early undetected pregnancy.

  8. Participant with adequate hematologic, renal and liver function at screening visit.

    a Absolute Neutrophil Count (ANC) with more, or equal than 1500/mm3 b Platelet count more, or equal than 75,000/mm3 c Hemoglobin ≥9.0 g/dL d Estimated Glomerular Filtration Rate (eGFR) of ≥30 mL/min/1.73 m2 by the CKD-EPI formula e Total Bilirubin <1.2 mg/dL f AST and ALT ≤2.5 × ULN (≤ 4 × ULN for liver metastasis)

  9. Participant willing and able to adhere to the lifestyle restrictions specified in this protocol

Exclusion Criteria:

Any potential participant who meets any of the following criteria will be excluded from participating in the study:

  1. Documented medical history of clinically significant cardiac, vascular, pulmonary, gastrointestinal, endocrine, neurologic, hematologic, rheumatologic, psychiatric, or metabolic disturbances or any other medical condition(s) for which, in the opinion of the investigator, participation would not be in the best interest of the participant (eg, compromise the wellbeing) or that could prevent, limit, or confound the protocol-specified assessments.
  2. Known allergies, hypersensitivity, or intolerance to any of the study interventions, or components/ excipients thereof, or drug or other allergy that, in the opinion of the investigator, contraindicates participation in the study.
  3. Prior doxorubicin exposure that would result in a total lifetime exposure of 450 mg/m2 or more after four cycles of treatment.
  4. Current active systemic opportunistic infection based on clinical assessment.
  5. Had major surgical procedure and will not have fully recovered from surgical procedure, or has surgical procedure planned during the time the participant is expected to participate in the study.
  6. Presence of hepatitis B surface antigen (HBsAg) or IgM anti-HBC at screening or within 3 months prior to first dose of investigational intervention.
  7. Positive hepatitis C antibody test result at screening or within 3 months prior to starting investigational intervention.
  8. Has known human immunodeficiency virus (HIV) seropositive status, or positive HIV antibody test at screening.
  9. History of drug or alcohol abuse according to medical history assessment by investigator within 1 year before screening.
  10. History of malignancy except disease under study within the past 3 years except for basal cell or squamous epithelial carcinomas of the skin that have been resected with no evidence of metastatic disease for 3 years; carcinoma in situ of the cervix; or malignancy, which is considered cured with minimal risk of recurrence.
  11. Known CNS disease, except for treated asymptomatic CNS metastases. Baseline brain imaging is not required for the eligibility assessment. Leptomeningeal disease is always an exclusion.
  12. Participant with known history or current symptoms of any of the following clinically significant cardiac conditions:

    a Unstable angina or myocardial infarction within the past 6 months. b New York Heart Association (NYHA) cardiac disease (Class II or greater) within past 6 months c High-risk uncontrolled arrythmias within past 6 months d Clinically significant pericardial disease within past 6 months e Electrocardiographic evidence of acute ischemic or active conduction system abnormalities within past 6 months f Any other cardiac illness that could lead to a safety risk to the study participant within past 6 months g Participant with a known left ventricular ejection fraction (LVEF) < 50% by echocardiogram or multigated acquisition scan (MUGA) within last 28 days before randomization h Study participants with known coronary artery disease, congestive heart failure not meeting the above criteria, must be on a stable medical regimen that is optimized in the opinion of the treating physician, in consultation with a cardiologist if appropriate.

  13. Received an investigational intervention or used an invasive investigational medical device within 6 months prior to baseline.
  14. Intended use of prohibited medications within 14 days prior to dosing and during the study.
  15. Positive Covid-19 RT-PCR test at the time of baseline within 72 hours before hospitalization.

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:他の
  • 割り当て:ランダム化
  • 介入モデル:クロスオーバー割り当て
  • 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:Test
Single application of 50mg/m2 by IV infusion
Pegylated liposomal doxorubicin hydrochloride concentrate for solution for infusion 2 mg/mL
アクティブコンパレータ:Comparator
Single application of 50mg/m2 by IV infusion
Pegylated liposomal doxorubicin hydrochloride concentrate for solution for infusion 2 mg/mL

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
Cmax for liposome encapsulated doxorubicin
時間枠:Up to 336 hours after drug administration
Maximum observed plasma concentration
Up to 336 hours after drug administration
AUC0-t for liposome encapsulated doxorubicin
時間枠:Up to 336 hours after drug administration
Area under the plasma concentration-time curve from time zero to the last quantifiable concentration
Up to 336 hours after drug administration

二次結果の測定

結果測定
メジャーの説明
時間枠
Cmax for free doxorubicin
時間枠:Up to 336 hours after drug administration
Maximum observed plasma concentration
Up to 336 hours after drug administration
AUC0-t for free doxorubicin
時間枠:Up to 336 hours after drug administration
Area under the plasma concentration-time curve from time zero to the last quantifiable concentration
Up to 336 hours after drug administration
AUC0-∞
時間枠:Up to 336 hours after drug administration
Area under the plasma concentration-time curve of rivastigmine from time zero to infinite
Up to 336 hours after drug administration
Tmax
時間枠:Up to 336 hours after drug administration
Time to reach Maximum observed plasma concentration
Up to 336 hours after drug administration
t1/2
時間枠:Up to 336 hours after drug administration
Half life
Up to 336 hours after drug administration
Vd
時間枠:Up to 336 hours after drug administration
Distribution Volume
Up to 336 hours after drug administration
Cl
時間枠:Up to 336 hours after drug administration
Clearence
Up to 336 hours after drug administration

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)

2023年2月13日

一次修了 (実際)

2023年6月22日

研究の完了 (実際)

2023年6月22日

試験登録日

最初に提出

2026年6月3日

QC基準を満たした最初の提出物

2026年6月9日

最初の投稿 (実際)

2026年6月15日

学習記録の更新

投稿された最後の更新 (実際)

2026年6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6月9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

IPD プランの説明

Individual participant data (IPD) will not be shared due to confidentiality restrictions and institutional policies regarding participant-level clinical data.

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

いいえ

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。

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Doxopeg® - Doxorubicin Hydrochloride Liposome Injection 20 mg/10 mL (2 mg/mL)の臨床試験

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