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- Klinische proef NCT07560943
Safety and Tolerability of AI-Designed Pan-Cancer Neoantigen mRNA Vaccine (PAN-NeoVax) in Advanced Solid Tumors
5 mei 2026 bijgewerkt door: Xingchen Peng, West China Hospital
A Phase I Clinical Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of an Artificial Intelligence-Designed Tumor mRNA Vaccine in Patients With Advanced or Metastatic Solid Tumors
This is a phase I, open-label, single-arm, single-center, dose-escalation study to evaluate the safety, tolerability, and preliminary anti-tumor efficacy of PAN-NeoVax, an artificial intelligence (AI)-designed pan-cancer neoantigen mRNA vaccine delivered via lipid nanoparticles (LNP), administered by intratumoral injection in patients with advanced or metastatic solid tumors who have failed second-line therapy.
The study employs a classical "3+3" dose-escalation design with three dose levels (25 μg, 50 μg, and 100 μg mRNA).
Each subject will receive 5 doses of basic immunization (first 4 doses at weekly intervals, fifth dose at 1 month after the fourth dose).
Studie Overzicht
Toestand
Werving
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Geschat)
9
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: Xingchen Peng
- Telefoonnummer: 18980606753
- E-mail: pxx2014@163.com
Studie Locaties
-
-
Sichuan
-
Chengdu, Sichuan, China, 610000
- Nog niet aan het werven
- West China Hospital
-
Contact:
- Xingchen Peng
- Telefoonnummer: 18980606753
- E-mail: pxx2014@163.com
-
Chengdu, Sichuan, China, 646000
- Werving
- The West China Hospital
-
-
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:
- Male or female patients aged ≥18 and ≤70 years
- Histopathologically confirmed advanced recurrent/metastatic malignant solid tumors that have failed second-line therapy with no standard treatment options available (priority enrollment of advanced head and neck squamous cell carcinoma and malignant melanoma patients)
- ECOG Performance Status score: 0-1
- Estimated life expectancy ≥3 months
- At least 28 days since prior chemotherapy, radiotherapy, or surgery
- At least 6 weeks since prior use of nitrosoureas or mitomycin C
Adequate organ function within 14 days prior to enrollment:
- Hemoglobin ≥90 g/L (no blood transfusion within 14 days)
- Absolute neutrophil count >1.5×10⁹/L
- Platelet count ≥80×10⁹/L
- Total bilirubin ≤1.5×ULN
- ALT or AST ≤2.5×ULN (≤5×ULN if liver metastases present)
- Creatinine clearance ≥60 mL/min (Cockcroft-Gault formula)
- Left ventricular ejection fraction (LVEF) ≥50%
- Signed written informed consent and willingness to comply with scheduled visits, treatment plans, laboratory tests, and other study requirements
Exclusion Criteria:
- Participation in another clinical drug trial within 4 weeks
- Tumor located adjacent to major blood vessels or trachea
- Poorly controlled cardiac conditions: NYHA class >2 heart failure, unstable angina, myocardial infarction within 1 year, or clinically significant supraventricular or ventricular arrhythmias requiring treatment or intervention
- Pregnant or breastfeeding women
- Active pulmonary tuberculosis, bacterial or fungal infection (≥Grade 2 per NCI-CTCAE v5.0); HIV infection, active HBV or HCV infection
- History of psychotropic substance abuse that cannot be discontinued, or mental disorders
- Active autoimmune disease or history of autoimmune disease (exceptions: vitiligo; childhood asthma in complete remission requiring no adult intervention; asthma requiring bronchodilator intervention is excluded)
- Currently receiving immunosuppressive therapy
- History of drug abuse or known medical, psychological, or social conditions (e.g., alcoholism, drug addiction)
- Known allergy, hypersensitivity, or intolerance to PAN-NeoVax or any excipient; history of severe allergic reactions to any drug, food, or vaccine (including anaphylactic shock, allergic laryngeal edema, allergic dyspnea, allergic purpura, thrombocytopenic purpura, Arthus reaction)
- Female subjects with pregnancy plans or male subjects whose partners have pregnancy plans from screening through 12 months after the last dose
- Any serious concomitant disease that, in the investigator's judgment, would jeopardize patient safety or ability to complete the study
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: Sequentiële toewijzing
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: PAN-NeoVax Dose Level 1 (25 μg)
|
25 μg PAN-NeoVax administered by intratumoral injection; 5 doses of basic immunization (first 4 doses at weekly intervals, fifth dose at 1 month after the fourth dose).
|
|
Experimenteel: PAN-NeoVax Dose Level 2 (50 μg)
|
50 μg PAN-NeoVax administered by intratumoral injection; 5 doses of basic immunization (first 4 doses at weekly intervals, fifth dose at 1 month after the fourth dose).
|
|
Experimenteel: PAN-NeoVax Dose Level 3 (100 μg)
|
100 μg PAN-NeoVax administered by intratumoral injection; 5 doses of basic immunization (first 4 doses at weekly intervals, fifth dose at 1 month after the fourth dose).
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Number of Participants with DLT
Tijdsspanne: From the first dose to 3 weeks post-dose.
|
From the first dose to 3 weeks post-dose.
|
Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Objective Response Rate
Tijdsspanne: From the time when the patients were enrolled in the study until one month after the last dose was injected.The time window was typically 2 months.
|
From the time when the patients were enrolled in the study until one month after the last dose was injected.The time window was typically 2 months.
|
|
Disease Control Rate
Tijdsspanne: From the time when the patients were enrolled in the study until one month after the last dose was injected.The time window was typically 2 months.
|
From the time when the patients were enrolled in the study until one month after the last dose was injected.The time window was typically 2 months.
|
|
Time to First Response
Tijdsspanne: From the time when the patients were enrolled in the study until one month after the last dose was injected.The time window was typically 2 months.
|
From the time when the patients were enrolled in the study until one month after the last dose was injected.The time window was typically 2 months.
|
|
Duration of Response
Tijdsspanne: From the time when the patients were enrolled in the study until one month after the last dose was injected.The time window was typically 2 months.
|
From the time when the patients were enrolled in the study until one month after the last dose was injected.The time window was typically 2 months.
|
|
Progression - Free Survival(PFS)
Tijdsspanne: From the time when the patients were enrolled in the study until three months after the last dose was injected. The time window was typically 6 months.
|
From the time when the patients were enrolled in the study until three months after the last dose was injected. The time window was typically 6 months.
|
|
Overall Survival(OS)
Tijdsspanne: From the time when the patients were enrolled in the study until six months after the last dose was injected. The time window was typically 8 months.
|
From the time when the patients were enrolled in the study until six months after the last dose was injected. The time window was typically 8 months.
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
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 (Geschat)
28 april 2026
Primaire voltooiing (Geschat)
28 april 2027
Studie voltooiing (Geschat)
28 december 2027
Studieregistratiedata
Eerst ingediend
24 april 2026
Eerst ingediend dat voldeed aan de QC-criteria
24 april 2026
Eerst geplaatst (Werkelijk)
1 mei 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
11 mei 2026
Laatste update ingediend die voldeed aan QC-criteria
5 mei 2026
Laatst geverifieerd
1 april 2026
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 2026(826)
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 .