- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07660211
Clinical Evaluation of 177Lu-PSMA-VG01 Injection in Patients With PSMA-Positive Metastatic Castration-Resistant Prostate Cancer (mCRPC)
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)
Studienübersicht
Status
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Einschreibung (Geschätzt)
Phase
- Phase 1
Kontakte und Standorte
Studienkontakt
- Name: Xiaobo Su
- Telefonnummer: 086+0632-2989679
- E-Mail: xiaobo.su@vitsgen.com
Studienorte
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, China, 200032
- Rekrutierung
- Zhong Shan Hospital Fudan University
-
Kontakt:
- Hongcheng Shi, Doctor of Medicine
- Telefonnummer: 086+ 021-64041990
- E-Mail: shi.hongcheng@zs-hospital.sh.cn
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Male participants aged 18 years (inclusive) to 80 years (exclusive) at the time of signing the informed consent.
- Histologically or cytologically confirmed prostate cancer with no standard treatment options available, or failure/intolerance to standard therapies, or inability to access standard treatment.
- During the screening period, imaging examinations (within 4 weeks before administration) showed the presence of ≥1 metastatic lesion.
- ECOG Performance Status score: 0 to 2.
- Expected survival time exceeds 6 months.
- 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).
- The participant must be fully informed about the study and voluntarily provide written informed consent prior to participation.
- The participant must be capable of understanding and complying with the requirements of the trial protocol.
- 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:
- 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.
- Having received systemic or local radionuclide therapy within 3 months prior to the first dose.
- 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.
- 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.
- 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).
- Having symptomatic spinal cord compression or clinical/imaging findings suggestive of impending spinal cord compression.
- Known allergy to structural analogs of this product or other excipients.
- 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.
- 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.
- Having uncontrolled third-space fluid accumulations (such as significant pleural effusion, ascites or pericardial effusion) deemed unsuitable for enrollment by the investigator.
- Having a clear history of neurological or psychiatric disorders, including epilepsy or dementia.
- Other reasons considered by the investigator to make the participant unsuitable for participation in this clinical study.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: 177Lu-PSMA-VG01 Injection
Successfully screened participants will be treated with 177Lu-PSMA-VG01 Injection during the treatment period .
|
Treatment patients
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Radiation dosimetry
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: Up to 6 weeks
|
Evaluating the safety and tolerability of the 177Lu-PSMA-VG01 injection in participants.
|
Up to 6 weeks
|
|
AE
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: Up to 8 days .
|
Pharmacokinetics (PK) of 177Lu-PSMA-VG01 in plasma
|
Up to 8 days .
|
|
Maximum plasma concentration (Cmax)
Zeitfenster: Up to 8 days .
|
Pharmacokinetics (PK) of 177Lu-PSMA-VG01 in plasma
|
Up to 8 days .
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Objective Response Rate (ORR)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: From baseline to 36 weeks
|
PSA50 response rate and PSA90 response rate
|
From baseline to 36 weeks
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Andere Studien-ID-Nummern
- 2026-078R
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur 177Lu-PSMA-VG01
-
Peter MacCallum Cancer Centre, AustraliaAktiv, nicht rekrutierendProstatakrebs | Metastasierter kastrationsresistenter ProstatakrebsAustralien
-
Peter MacCallum Cancer Centre, AustraliaEndocyte; Movember Foundation; Medical Research Future Fund; E.J. Whitten Foundation...Aktiv, nicht rekrutierendDosimetrie, Sicherheit und potenzieller Nutzen von 177Lu-PSMA-617 vor der Prostatektomie (LuTectomy)ProstataneoplasmenAustralien
-
Sidney Kimmel Comprehensive Cancer Center at Johns...Adenoid Cystic Carcinoma Research Foundation; Progenics Pharmaceuticals, Inc.BeendetAdenoidzystisches KarzinomVereinigte Staaten
-
Peking Union Medical College HospitalRekrutierungMetastasierter kastrationsresistenter ProstatakrebsChina
-
Peking University First HospitalNoch keine Rekrutierung
-
The First Affiliated Hospital of Xiamen UniversityAbgeschlossenMetastasierter kastrationsresistenter Prostatakrebs, mCRPCChina
-
Nanjing First Hospital, Nanjing Medical UniversityRekrutierung
-
Chengdu StarRay Therapeutics Co., LtdNoch keine RekrutierungMetastasierter kastrationsresistenter Prostatakrebs (mCRPC)
-
Medical University of ViennaRekrutierung
-
Jinming ZhangSinotau Pharmaceutical GroupRekrutierung