Safety and Tolerability of AI-Designed Pan-Cancer Neoantigen mRNA Vaccine (PAN-NeoVax) in Advanced Solid Tumors
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
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Tipo di studio
Tipo di studio
Iscrizione (Stimato)
Iscrizione
Fase
Fase
- Fase 1
Contatti e Sedi
Contatto studio
Contatto studio
- Nome: Xingchen Peng
- Numero di telefono: 18980606753
- Email: pxx2014@163.com
Luoghi di studio
-
-
Sichuan
-
Chengdu, Sichuan, Cina, 610000
- Non ancora reclutamento
- West China Hospital
-
Contatto:
- Xingchen Peng
- Numero di telefono: 18980606753
- Email: pxx2014@163.com
-
Chengdu, Sichuan, Cina, 646000
- Reclutamento
- The West China Hospital
-
-
Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
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
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione sequenziale
- Mascheramento: Nessuno (etichetta aperta)
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
|---|---|
|
Sperimentale: 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).
|
|
Sperimentale: 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).
|
|
Sperimentale: 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).
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Number of Participants with DLT
Lasso di tempo: From the first dose to 3 weeks post-dose.
|
From the first dose to 3 weeks post-dose.
|
Misure di risultato secondarie
Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Objective Response Rate
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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.
|
Collaboratori e investigatori
Sponsor
Sponsor
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Inizio studio
Completamento primario (Stimato)
Completamento primario
Completamento dello studio (Stimato)
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- 2026(826)
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .