- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT07656116
Platform Study of VSV-Based Recombinant Oncolytic Viruses for the Treatment of Advanced Malignant Tumors
14 juni 2026 bijgewerkt door: Cancer Institute and Hospital, Chinese Academy of Medical Sciences
A Phase I Platform Study of VSV-Based Recombinant Oncolytic Viruses for the Treatment of Advanced Malignant Tumors
To evaluate the safety and tolerability of combined administration of VSV injection solutions carrying different targets via multiple routes for treating advanced malignant solid tumors.
Studie Overzicht
Toestand
Werving
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
This is an open-label, dose-escalation phase I clinical trial designed to evaluate the safety and tolerability of combined administration of vesicular stomatitis virus (VSV) injection solutions carrying different targets via multiple routes in patients with advanced malignant solid tumors, and to preliminarily explore the maximum tolerated dose (MTD), recommended phase II dose (RP2D), as well as the preliminary anti-tumor activity and pharmacokinetic (PK)/pharmacodynamic (PD) characteristics of this regimen.
Studietype
Ingrijpend
Inschrijving (Geschat)
27
Fase
- 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: Yanjie Han, MD
- Telefoonnummer: +86010-87788165
- E-mail: annyhan_1997@163.com
Studie Contact Back-up
- Naam: Shuhang Wang, MD
- Telefoonnummer: 13581809307
- E-mail: wangshuhang@cicams.ac.cn
Studie Locaties
-
-
Hebei
-
Langfang, Hebei, China
- Werving
- Cancer Hospital Chinese Academy of Medical Scienc
-
-
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:
- Voluntarily sign the informed consent form, understand this study, and agree to comply with the protocol and complete all trial procedures
- Be at least 18 years of age at the time of signing the ICF, with no gender restrictions.
- Patients with advanced solid tumors confirmed by histopathological/cytological examination of primary and/or metastatic lesions.
- Patients who have failed standard therapy, lack a standard last-line treatment option, or are medically ineligible for standard therapy.
- Subjects with an ECOG performance status of 0-2 and an estimated survival of ≥12 weeks.
- Adequate organ and hematopoietic function: Absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/LPlatelet count ≥ 75 × 10⁹/L (no platelet transfusion or thrombopoietin (TPO) therapy within 2 weeks prior to first dose)Hemoglobin ≥ 90 g/L (no blood transfusion within 2 weeks)Serum creatinine ≤ 1.5 × upper limit of normal (ULN) or creatinine clearance (CCr) ≥ 50 mL/min Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3.0 × ULN for patients with liver metastases, AST and ALT < 5 × ULN, Serum total bilirubin (TBIL) ≤ 2 × ULN, International Normalized Ratio (INR) ≤ 1.5 × ULN, or activated partial thromboplastin time (APTT) ≤ 1.5 × ULN
- Women of childbearing potential must have a negative pregnancy test within 7 days prior to treatment initiation.
- Male and female subjects of reproductive potential must agree to use reliable contraception during the trial and for at least 6 months after the last dose. Translated with DeepL.com (free version)
Exclusion Criteria:
- Subjects with other active malignancies within the past 5 years. Exceptions include subjects who have achieved complete remission and require no follow-up treatment, and subjects with malignancies within the scope of the indication.
- Lesions intended for injection with a maximum diameter >100 mm;
- Subjects who have participated in or are currently participating in other drug or medical device clinical trials within the past 4 weeks;
- Subjects scheduled for or who have previously undergone tissue/organ transplantation;
- Subjects with Human Immunodeficiency Virus (HIV) infection who have experienced AIDS-related opportunistic infections within the past 12 months, or who have a CD4+ T-cell (CD4+) count < 350 cells/uL Patients with positive hepatitis B surface antigen (HBsAg) and/or hepatitis B core antibody (HBcAb) at screening, with HBV-DNA above the lower limit of detection patients with positive HCV antibody at screening and HCV-RNA above the lower limit of detection subjects with positive syphilis serology
- Subjects requiring antiviral medication during the study period or within 5 half-lives of antiviral medication at the time of first dosing.
- Subjects requiring therapeutic anticoagulant medication during the study period.
- Subjects with uncontrolled active infection of ≥Grade 3 severity according to CTCAE v5.0 that is clinically significant
- Received antineoplastic therapy (chemotherapy, radiotherapy, biologic therapy, endocrine therapy, immunotherapy, etc.) within 4 weeks prior to first dose Received small-molecule targeted therapy or oral fluorouracil-based agents within 2 weeks prior to first dose or within 5 half-lives (whichever is longer) Received Chinese herbal medicine or proprietary Chinese medicine with antitumor indications within 2 weeks prior to first dose Received Chinese herbal medicine or proprietary Chinese medicine with antitumor indications within 2 weeks prior to first dose Received nitrosourea or mitomycin C within 6 weeks prior to first dose Palliative radiotherapy for non-target lesions is permitted (≥2 weeks prior to first dose)
- Uncontrolled hypertension, pulmonary hypertension, or unstable angina myocardial infarction, coronary artery bypass grafting, or stenting within 6 months prior to dosing history of chronic heart failure at New York Heart Association (NYHA) functional class III-IV Severe arrhythmias requiring treatment (excluding atrial fibrillation or paroxysmal supraventricular tachycardia deemed by the investigator to have no impact on the trial), including QTcF ≥ 450 ms in males or ≥ 470 ms in females (calculated using Fridericia's formula) cerebrovascular accident (CVA) or transient ischemic attack (TIA) within 6 months prior to enrollment
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: Niet-gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: VM7V02
VM7V02: 1 mL/vial, 6.0E10 PFU/mL,Administer twice every two weeks.
|
Administer twice every two weeks.
|
|
Experimenteel: VM8V02
VM8V02:1 mL/vial, 6.0E10 PFU/mL,Administer twice every two weeks.
|
Administer twice every two weeks.
|
|
Experimenteel: VM8V01
VM8V01: 1 mL/vial, 6.0E10 PFU/mL,Administer twice every two weeks.
|
Administer twice every two weeks.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Incidentie van Bijwerkingen (AEs)
Tijdsspanne: Van ondertekening ICF tot 24 maanden na de laatste infusie.
|
Incidentie en ernst van behandeling-gerelateerde ongewenste voorvallen (TEAEs) gegradeerd volgens NCI CTCAE v5.0.
|
Van ondertekening ICF tot 24 maanden na de laatste infusie.
|
|
Incidence of Dose-Limiting Toxicities (DLTs)
Tijdsspanne: Within 21 days after administration
|
Incidence and characteristics of DLTs graded according to NCI CTCAE v5.0.
The DLT observation period is 21 days post-administration.
|
Within 21 days after administration
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Duration of Response (DOR)
Tijdsspanne: Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
|
The time from the first documentation of objective tumor response (CR or PR) to the first documentation of objective tumor progression or death from any cause.
|
Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
|
|
Progression-Free Survival (PFS)
Tijdsspanne: Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
|
The time from the first dose of study drug until the first documentation of objective tumor progression or death from any cause.
|
Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
|
|
Overall Survival (OS)
Tijdsspanne: Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
|
The time from the first dose of study drug to death from any cause.
|
Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
|
|
Objective Response Rate (ORR)
Tijdsspanne: Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
|
Overall response rate assessed per RECIST 1.1
|
Imaging assessments will be conducted within 28 days prior to first dose, every 6 weeks (±7 days) during treatment, and every 12 weeks during follow-up until disease progression,up to 24 months.
|
|
Biodistribution and Viral Shedding of VSV
Tijdsspanne: Starting before the first dose and continuing until 28 days (±7 days) after the last dose
|
Measurement of VSV viral load/concentration in blood, urine, saliva, feces, and at the injection site to evaluate viral distribution and clearance.
|
Starting before the first dose and continuing until 28 days (±7 days) after the last dose
|
|
Changes in Peripheral Blood Cytokine Levels
Tijdsspanne: Starting before the first dose and continuing until 28 days (±7 days) after the last dose
|
Assessment of cytokine levels following VSV injection.
|
Starting before the first dose and continuing until 28 days (±7 days) after the last dose
|
|
Changes in C-reactive Protein (CRP) Levels
Tijdsspanne: Starting before the first dose and continuing until 28 days (±7 days) after the last dose
|
Assessment of systemic inflammatory response by measuring serum CRP levels.
|
Starting before the first dose and continuing until 28 days (±7 days) after the last dose
|
|
Changes in Peripheral Lymphocyte Subsets
Tijdsspanne: Starting before the first dose and continuing until 28 days (±7 days) after the last dose
|
Assessment of the proportions and/or absolute counts of T cells, B cells, and NK cells in peripheral blood.
|
Starting before the first dose and continuing until 28 days (±7 days) after the last dose
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Onderzoekers
- Studie directeur: Shuhang Wang, Cancer Institute and Hospital, Chinese Academy of Medical Sciences
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)
29 januari 2026
Primaire voltooiing (Geschat)
31 januari 2027
Studie voltooiing (Geschat)
31 januari 2027
Studieregistratiedata
Eerst ingediend
28 januari 2026
Eerst ingediend dat voldeed aan de QC-criteria
14 juni 2026
Eerst geplaatst (Werkelijk)
18 juni 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
18 juni 2026
Laatste update ingediend die voldeed aan QC-criteria
14 juni 2026
Laatst geverifieerd
1 juni 2026
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Andere studie-ID-nummers
- VSV-A01
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 .
Klinische onderzoeken op Geavanceerde vaste tumor
-
Jun wangNog niet aan het wervenTrombocytopenie | Solid tumor -maligniteiten, kanker | CTIT-chemotherapie-geïnduceerde trombocytopenieChina
-
Shanghai Henlius BiotechWerving
-
Changchun GeneScience Pharmaceutical Co., Ltd.WervingSolid tumoren die een TP53 Y220C -mutatie herbergenChina
-
AbbVieWervingSolid tumoren herbergen ontmoet versterkingVerenigde Staten, Israël, Japan, Zuid -Korea, Spanje
-
Shanghai Zhongshan HospitalNog niet aan het wervenMaag Adenocarcinoom | Gastro-oesofageaal adenocarcinoom | Immunotherapie | Mismatch Repair Deficient of MSI-High Solid Tumors
-
Shanghai Zhongshan HospitalNog niet aan het wervenImmunotherapie | Mismatch Repair Deficient of MSI-High Solid Tumors | Maag-/gastro-oesofageale verbinding Adenocarcinoom
-
Azienda Ospedaliera Universitaria Integrata VeronaVoltooidScaphoid Non-Union Advanced Collapse (SNAC pols)
-
Extremity MedicalWervingArtrose | Inflammatoire artritis | Carpaal Tunnel Syndroom (CTS) | Posttraumatische artritis | Scapholunate geavanceerde instorting (SLAC) | Scapholunaat Crystalline Advanced Collapse (SCAC) | Scaphoid, Trapezium en Trapezoid Advanced Collapse (STTAC) | Ziekte van Kienbock bij volwassenen | Radiale... en andere voorwaardenVerenigde Staten
-
Advanced BionicsVoltooidErnstig tot zeer ernstig gehoorverlies | bij volwassen gebruikers van Advanced Bionics HiResolution™ Bionic Ear SystemVerenigde Staten
-
Shanghai Zhongshan HospitalNog niet aan het wervenMismatch Repair Deficient of MSI-High Solid Tumors | Lymfekliermetastasen | Maag-/gastro-oesofageale verbinding Adenocarcinoom | Lymphatic Invasion
Klinische onderzoeken op VSV injection
-
Zhuhai Trinomab Pharmaceutical Co., Ltd.Werving
-
HealthBeacon PlcModena Allergy & AsthmaAanmelden op uitnodiging
-
SymateseWervingNeus-lippenplooi Rimpels | Wangvergroting | Infraorbitale holtes | Verbetering van de lippen | Periorale rimpelsFrankrijk
-
University Hospital, GenevaWellcome Trust; KEMRI-Wellcome Trust Collaborative Research Program; World Health... en andere medewerkersVoltooid
-
University of OxfordUniversity Hospital, Geneva; Wellcome Trust; World Health Organization; Universitätsklinikum... en andere medewerkersOnbekend
-
Mayo ClinicNational Cancer Institute (NCI)BeëindigdGemetastaseerd melanoom | Gemetastaseerd oogmelanoom | Inoperabel melanoom | Klinisch stadium III huidmelanoom AJCC v8 | Pathologisch stadium IIIB Cutaan melanoom AJCC v8 | Pathologisch stadium IIIC Cutaan melanoom AJCC v8 | Pathologisch stadium IIID Cutaan melanoom AJCC v8 | Pathologisch stadium... en andere voorwaardenVerenigde Staten
-
The First Affiliated Hospital of Xinxiang Medical...WervingMelanoma | Borstkanker | Longkanker | Geavanceerde vaste tumor | Immunotherapie | KankerbehandelingChina
-
Union Hospital, Tongji Medical College, Huazhong...WervingKwaadaardige tumoren | HUISDIER | SSTR2China
-
Boehringer IngelheimBoehringer IngelheimActief, niet wervendDuctaal adenocarcinoom van de alvleesklierVerenigde Staten, Spanje, Zwitserland, Duitsland
-
Cairo UniversityNog niet aan het wervenPijn beoordeling