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- Klinische proef NCT07808177
Clinical Evaluation of 177Lu-FAP-VG11 Injection in Patients With Fibroblast Activation Protein -Positive Advanced Solid Tumours
9 september 2026 bijgewerkt door: Xiaorong Sun, Shandong Cancer Hospital and Institute
An Exploratory Clinical Study to Evaluate the Safety, Tolerability and Biodistribution Characteristics of 177 Lu FAP VG11 Injection in Patients With Advanced Solid Tumours
This is an exploratory clinical study evaluating the safety, tolerability and biodistribution characteristics of 177Lu-FAP-VG11 injection in patients with FAP-positive advanced solid tumours.
Studie Overzicht
Toestand
Werving
Interventie / Behandeling
Gedetailleerde beschrijving
This is an exploratory, single-arm, dose-escalation, open-label early Phase I clinical study to evaluate the safety, tolerability, dosimetry and preliminary efficacy of 177Lu-FAP-VG11 injection in FAP-positive patients with advanced solid tumors.
Studietype
Ingrijpend
Inschrijving (Geschat)
7
Fase
- Vroege fase 1
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Xiaorong Sun
- Telefoonnummer: 0531-67626287
- E-mail: xrsun@sdfmu.edu.cn
Studie Locaties
-
-
Shandong
-
Jinan, Shandong, China, 250000
- Werving
- Cancer Hospital of Shandong First Medical University
-
Contact:
- Xiaorong Sun
- Telefoonnummer: 0531-67626287
- E-mail: xrsun@sdfmu.edu.cn
-
-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Nee
Beschrijving
Inclusion Criteria:
- Patients with advanced solid tumors who have failed standard therapy or for whom no standard therapy is available.
- Patients whose tumors are assessed as FAP-positive (high FAP expression with SUVmax uptake above liver background) by FAP-targeted diagnostic PET/CT imaging.
- In the investigator's judgment, no other treatment option with curative or life-prolonging potential is available.
- Male or non-pregnant, non-lactating females, aged ≥18 years.
- Eastern Cooperative Oncology Group (ECOG) performance status score ≤2.
- Life expectancy >6 months.
- Female patients: Women of childbearing potential must agree to use highly effective contraceptive methods from screening until 6 months after the last dose of study drug.
- Male patients: Subjects must use a condom during sexual intercourse during the study and for 14 weeks after the last study treatment to prevent partner pregnancy and to avoid transmission of the study drug via semen; in addition, subjects should refrain from sperm donation during treatment and for 6 months after the last study drug administration.
- Subjects must provide written informed consent voluntarily before participation in the trial.
- Willing and able to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures.
Exclusion Criteria:
- Clinically symptomatic central nervous system metastases or meningeal metastases, or other evidence that the patient's central nervous system or meningeal metastases are not controlled, and deemed unsuitable for enrollment by the investigator.
- Major organ surgery (excluding needle biopsy) or significant trauma within 4 weeks prior to the first use of study drug, or need for elective surgery during the study period.
- History of immunodeficiency, including positive HIV test, or other acquired or congenital immunodeficiency diseases, or history of organ transplantation, or severe autoimmune disease history deemed unsuitable for enrollment by the investigator; or allogeneic organ transplantation requiring immunosuppressive therapy.
- Receipt of systemic or local radioisotope therapy within 3 months prior to the first dose.
- Receipt of other investigational drugs not yet marketed within 4 weeks prior to the first use of study drug, or within five half-lives of the other investigational drug.
- Definitive history of neurological or psychiatric disorders, including epilepsy or dementia.
- Pregnancy or lactation, or unwillingness to use adequate contraceptive methods.
- Any severe concomitant disease that, in the investigator's opinion, would make the patient's participation in the study inadvisable or could affect compliance with the protoco.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: 177Lu-FAP-VG11 injection treatment
Patients will be treated with 177Lu-FAP-VG11 Injection
|
Patients will receive 177Lu-FAP-VG11 administration at an interval of 6 weeks between each dose.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Dose-Limiting Toxicities (DLT)
Tijdsspanne: Through study completion, assessed up to 2 years.
|
Evaluating the safety and tolerability of the 177Lu-FAP-VG11 injection in patients.
|
Through study completion, assessed up to 2 years.
|
|
Maximum Tolerate dose (MTD)
Tijdsspanne: Through study completion, assessed up to 2 years.
|
Evaluating the safety and tolerability of the 177Lu-FAP-VG11 injection in patients.
|
Through study completion, assessed up to 2 years.
|
|
Adverse Events
Tijdsspanne: Through study completion, assessed up to 2 years.
|
Patients adverse events Incidence and severity of treatment emergent adverse events will be assessed as per CTCAE v6.0.All Adverse Events (AEs) occurring during the clinical study period will be monitored.
|
Through study completion, assessed up to 2 years.
|
|
Biodistribution
Tijdsspanne: Through study completion, assessed up to 2 years.
|
Evaluation of drug biodistribution in major human organs.
|
Through study completion, assessed up to 2 years.
|
|
Radiation dosimetry
Tijdsspanne: Through study completion, assessed up to 2 years.
|
Standard uptake value (SUV).
|
Through study completion, assessed up to 2 years.
|
|
Radiation dosimetry
Tijdsspanne: Through study completion, assessed up to 2 years.
|
Organ accumulation (%ID).
|
Through study completion, assessed up to 2 years.
|
|
Radiation dosimetry
Tijdsspanne: Through study completion, assessed up to 2 years.
|
Absorbed dose (AD).
|
Through study completion, assessed up to 2 years.
|
|
Radiation dosimetry
Tijdsspanne: Through study completion, assessed up to 2 years.
|
Effective dose (ED) in tumors and target organs.
|
Through study completion, assessed up to 2 years.
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Objective Response Rate (ORR)
Tijdsspanne: Through study completion, assessed up to 2 years.
|
ORR is defined as the the proportion of subjects who achieve a best overall response of Complete Response (CR) or Partial Response (PR).
|
Through study completion, assessed up to 2 years.
|
|
Duration of Response (DOR)
Tijdsspanne: Through study completion, assessed up to 2 years.
|
DOR is defined as the time from the earliest date of documented CR or PR until documented disease progression or death, whichever occurs first.
|
Through study completion, assessed up to 2 years.
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
17 juni 2026
Primaire voltooiing (Geschat)
6 mei 2027
Studie voltooiing (Geschat)
6 mei 2029
Studieregistratiedata
Eerst ingediend
18 augustus 2026
Eerst ingediend dat voldeed aan de QC-criteria
6 september 2026
Eerst geplaatst (Werkelijk)
8 september 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
14 september 2026
Laatste update ingediend die voldeed aan QC-criteria
9 september 2026
Laatst geverifieerd
1 augustus 2026
Meer informatie
Termen gerelateerd aan deze studie
Andere studie-ID-nummers
- SDZLEC2026-049-001
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .