- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07560943
Safety and Tolerability of AI-Designed Pan-Cancer Neoantigen mRNA Vaccine (PAN-NeoVax) in Advanced Solid Tumors
5 mai 2026 mis à jour par: 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).
Aperçu de l'étude
Statut
Recrutement
Les conditions
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Estimé)
9
Phase
- La phase 1
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Xingchen Peng
- Numéro de téléphone: 18980606753
- E-mail: pxx2014@163.com
Lieux d'étude
-
-
Sichuan
-
Chengdu, Sichuan, Chine, 610000
- Pas encore de recrutement
- West China Hospital
-
Contact:
- Xingchen Peng
- Numéro de téléphone: 18980606753
- E-mail: pxx2014@163.com
-
Chengdu, Sichuan, Chine, 646000
- Recrutement
- The West China Hospital
-
-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
La description
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
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation séquentielle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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).
|
|
Expérimental: 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).
|
|
Expérimental: 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).
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Number of Participants with DLT
Délai: From the first dose to 3 weeks post-dose.
|
From the first dose to 3 weeks post-dose.
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
Objective Response Rate
Délai: 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
Délai: 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
Délai: 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
Délai: 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)
Délai: 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)
Délai: 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.
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Estimé)
28 avril 2026
Achèvement primaire (Estimé)
28 avril 2027
Achèvement de l'étude (Estimé)
28 décembre 2027
Dates d'inscription aux études
Première soumission
24 avril 2026
Première soumission répondant aux critères de contrôle qualité
24 avril 2026
Première publication (Réel)
1 mai 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
11 mai 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
5 mai 2026
Dernière vérification
1 avril 2026
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 2026(826)
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .