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Clinical Evaluation of 177Lu-PSMA-VG01 Injection in Patients With PSMA-Positive Metastatic Castration-Resistant Prostate Cancer (mCRPC)

2026年6月15日 更新者:VitsGen Therapeutics Inc.

A Phase 1, Dose-Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Biodistribution, Radiation Dosimetry and Preliminary Efficacy of 177Lu-PSMA-VG01 Injection in Patients With PSMA-Positive Metastatic Castration-Resistant Prostate Cancer (mCRPC)

This is a phase I clinical trial conducted in participants with PSMA-positive metastatic castration-resistant prostate cancer (mCRPC). After confirmation of PSMA positivity, participants receive intravenous administration of 177Lu-PSMA-VG01. The objectives are: to evaluate the biodistribution, radiation dosimetry, safety and tolerability of 177Lu-PSMA-VG01 in participants; and to assess the pharmacokinetics (PK), preliminary anti-tumor activity, and in vivo stability of 177Lu-PSMA-VG01 in participants.

調査の概要

詳細な説明

This is a prospective, single-arm, dose-escalation and open phase I clinical study. 10-24 participants are expected to be enrolled. Participants will sign the informed consent form (ICF) prior to screening.

Only PSMA-positive participants with metastatic castration-resistant prostate cancer (mCRPC) who meet the inclusion criteria and do not meet any exclusion criteria will be enrolled. The successful screened participants will be treated with 177Lu-PSMA-VG01 injection intravenously during the treatment period. Pharmacokinetic (PK) blood samples will be collected, and SPECT/CT imaging will be performed during the clinical study.

Long-term follow-up will last up to 2 years after completion of EOT. Throughout the study period, participants will undergo safety monitoring following drug administration.

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

    • Shanghai Municipality
      • Shanghai、Shanghai Municipality、中国、200032
        • 募集
        • Zhong Shan Hospital Fudan University
        • 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

  • 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. Male participants aged 18 years (inclusive) to 80 years (exclusive) at the time of signing the informed consent.
  2. Histologically or cytologically confirmed prostate cancer with no standard treatment options available, or failure/intolerance to standard therapies, or inability to access standard treatment.
  3. During the screening period, imaging examinations (within 4 weeks before administration) showed the presence of ≥1 metastatic lesion.
  4. ECOG Performance Status score: 0 to 2.
  5. Expected survival time exceeds 6 months.
  6. All clinically significant toxicities related to prior anti-tumor therapy (e.g., chemotherapy, radiotherapy, etc., excluding Luteinizing Hormone-Releasing Hormone (LHRH) analog therapy) must have resolved to ≤ Grade 1, except for toxicities deemed safe and manageable by the investigator, such as alopecia, peripheral neuropathy ≤ Grade 2, etc. (CTCAE V6.0).
  7. The participant must be fully informed about the study and voluntarily provide written informed consent prior to participation.
  8. The participant must be capable of understanding and complying with the requirements of the trial protocol.
  9. The participant must use a condom during sexual activity throughout the study period and for 14 weeks after the last dose of study treatment to prevent pregnancy in partners and potential exposure of partners to the investigational product g via semen. Additionally, the participant should refrain from sperm donation during the specified timeframe above.

Exclusion Criteria:

  1. Having received anti-tumor therapies such as chemotherapy, biological therapy, targeted therapy, or immunotherapy within 4 weeks prior to the first dose of the investigational product, or planning to receive such therapies during the study period.
  2. Having received systemic or local radionuclide therapy within 3 months prior to the first dose.
  3. Having received other investigational product treatments not yet approved within 4 weeks prior to the first dose of the investigational product, or within five half-lives of that.
  4. Having undergone major organ surgery (excluding needle biopsy) or experienced significant trauma within 4 weeks prior to the first dose of the investigational product, or requiring elective surgery during the trial period.
  5. Having been diagnosed with other malignancies within the past 2 years (participants with a prior history of malignancy who have received adequate treatment and have remained disease- and treatment-free for over 3 years prior to enrollment are eligible, as are patients with adequately treated non-melanoma skin cancer or superficial bladder cancer).
  6. Having symptomatic spinal cord compression or clinical/imaging findings suggestive of impending spinal cord compression.
  7. Known allergy to structural analogs of this product or other excipients.
  8. Having a history of immunodeficiency, including a positive HIV test result, other acquired or congenital immunodeficiency diseases, or a history of organ transplantation; a history of severe autoimmune diseases deemed unsuitable for enrollment by the investigator; or requiring immunosuppressive therapy for allogeneic organ transplantation.
  9. Having severe infections (requiring intravenous antibiotics, antifungals, or antivirals according to clinical practice guidelines), active hepatitis A, active hepatitis B (HBV DNA ≥2000 IU/mL or 10^4 copies/mL; prophylactic antiviral therapy other than interferon is allowed), active hepatitis C (anti-HCV positive and HCV-RNA above the lower limit of detection), or active syphilis infection.
  10. Having uncontrolled third-space fluid accumulations (such as significant pleural effusion, ascites or pericardial effusion) deemed unsuitable for enrollment by the investigator.
  11. Having a clear history of neurological or psychiatric disorders, including epilepsy or dementia.
  12. Other reasons considered by the investigator to make the participant unsuitable for participation in this clinical study.

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:177Lu-PSMA-VG01 Injection
Successfully screened participants will be treated with 177Lu-PSMA-VG01 Injection during the treatment period .
Treatment patients

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
Radiation dosimetry
時間枠:Up to 36 weeks
Standard uptake value (SUV), organ accumulation (%ID), absorbed dose (AD), and effective dose (ED) in tumors and target organs
Up to 36 weeks
Dose-Limiting Toxicities (DLT)
時間枠:Up to 6 weeks
Evaluating the safety and tolerability of the 177Lu-PSMA-VG01 injection in participants.
Up to 6 weeks
Maximum Tolerate dose(MTD)
時間枠:Up to 6 weeks
Evaluating the safety and tolerability of the 177Lu-PSMA-VG01 injection in participants.
Up to 6 weeks
AE
時間枠:Up to 36 weeks

Evaluating the safety and tolerability of the 177Lu-PSMA-VG01 injection in participants.

All Adverse Events (AEs) occurring during the clinical study period will be monitored.

Up to 36 weeks
Accumulation (%ID)
時間枠:Up to 36 weeks
Evaluation of drug biodistribution in major human organs.
Up to 36 weeks
Area under the plasma concentration-time curve from time zero to the last measurable concentration(AUC₀-last)
時間枠:Up to 8 days.
Pharmacokinetics (PK) of 177Lu-PSMA-VG01 in plasma
Up to 8 days.
Area under the plasma concentration-time curve from time zero extrapolated to infinite time (AUC0-inf)
時間枠:Up to 8 days .
Pharmacokinetics (PK) of 177Lu-PSMA-VG01 in plasma
Up to 8 days .
Maximum plasma concentration (Cmax)
時間枠:Up to 8 days .
Pharmacokinetics (PK) of 177Lu-PSMA-VG01 in plasma
Up to 8 days .

二次結果の測定

結果測定
メジャーの説明
時間枠
Objective Response Rate (ORR)
時間枠:Up to 2 years after completing the End-of-Treatment visit.
Up to 2 years after completing the End-of-Treatment visit.
radiographic Progression-Free Survival (rPFS)
時間枠:Up to 2 years after completing the End-of-Treatment visit.
Up to 2 years after completing the End-of-Treatment visit.
PSA response rate
時間枠:From baseline to 36 weeks
PSA50 response rate and PSA90 response rate
From baseline to 36 weeks

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。

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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 (推定)

2026年6月16日

一次修了 (推定)

2027年5月6日

研究の完了 (推定)

2029年5月6日

試験登録日

最初に提出

2026年5月7日

QC基準を満たした最初の提出物

2026年6月15日

最初の投稿 (実際)

2026年6月22日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月22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15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

その他の研究ID番号

  • 2026-078R

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

いいえ

米国FDA規制機器製品の研究

いいえ

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