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

2026년 6월 15일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (추정된)

10

단계

  • 1단계

연락처 및 위치

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연구 연락처

연구 장소

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, 중국, 200032
        • 모병
        • Zhong Shan Hospital Fudan University
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 177Lu-PSMA-VG01 Injection
Successfully screened participants will be treated with 177Lu-PSMA-VG01 Injection during the treatment period .
Treatment patients

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Radiation dosimetry
기간: 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)
기간: 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)
기간: Up to 6 weeks
Evaluating the safety and tolerability of the 177Lu-PSMA-VG01 injection in participants.
Up to 6 weeks
AE
기간: 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)
기간: 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)
기간: 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)
기간: Up to 8 days .
Pharmacokinetics (PK) of 177Lu-PSMA-VG01 in plasma
Up to 8 days .
Maximum plasma concentration (Cmax)
기간: Up to 8 days .
Pharmacokinetics (PK) of 177Lu-PSMA-VG01 in plasma
Up to 8 days .

2차 결과 측정

결과 측정
측정값 설명
기간
Objective Response Rate (ORR)
기간: 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)
기간: 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
기간: From baseline to 36 weeks
PSA50 response rate and PSA90 response rate
From baseline to 36 weeks

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 6월 16일

기본 완료 (추정된)

2027년 5월 6일

연구 완료 (추정된)

2029년 5월 6일

연구 등록 날짜

최초 제출

2026년 5월 7일

QC 기준을 충족하는 최초 제출

2026년 6월 15일

처음 게시됨 (실제)

2026년 6월 22일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 22일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 15일

마지막으로 확인됨

2026년 6월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • 2026-078R

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

177Lu-PSMA-VG01에 대한 임상 시험

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