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OncoMatch/Clinical Trials/NCT07752953

Personalized Neoantigen-pulsed Autologous Dendritic Cell Injections for Malignant Solid Tumors

Is NCT07752953 recruiting? Yes, currently enrolling (Sep 2026). This NA trial studies multiple treatments including Personalized neoantigen-pulsed autologous dendritic cell Injections (ZSNeo-DC) and Immune Checkpoint Inhibitors for advanced solid tumor.

NARecruitingZSky Biotech IncNCT07752953Data as of Sep 2026Location: China

Treatment: Personalized neoantigen-pulsed autologous dendritic cell Injections (ZSNeo-DC) · Immune Checkpoint InhibitorsThis is a prospective, single-center, open-label, real-world clinical study designed to evaluate the safety, efficacy, and immunogenicity of Personalized neoantigen-pulsed autologous dendritic cell Injections (ZSNeo-DC)in patients with malignant solid tumors. The study protocol received approval from the institutional review board and ethics committee of Beidaihe Hospital, adhering to ethical guidelines. Written informed consent was obtained from all participants in accordance with the principles of the Declaration of Helsinki. Approximately 100 patients will be enrolled in multiple tumor-specific cohorts which will be independently statistically analyzed. ZSNeo-DC will be manufactured by Good Manufacturing Practice (GMP). Participants will receive seven subcutaneous injections of personalized DCs administered on Days 1, 8, 15, 22, 36, 50, and 64, either as monotherapy or in combination with immune checkpoint inhibitors according to routine clinical practice. Tumor response, progression-free survival, overall survival, safety, and antigen-specific immune responses will be evaluated throughout the study.

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Extracted eligibility criteria

Treatments studied

Other

Personalized neoantigen-pulsed autologous dendritic cell Injections (ZSNeo-DC)Immune Checkpoint Inhibitors

Cancer type

Tumor Agnostic

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

Cannot have received: allogeneic hematopoietic stem cell transplantation

Previous allogeneic hematopoietic stem cell transplantation

Cannot have received: solid organ transplantation

Previous solid organ transplantation

Lab requirements

Blood counts

adequate hematologic function

Kidney function

adequate renal function

Liver function

adequate hepatic function

Cardiac function

left ventricular ejection fraction (lvef) ≥50%

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07752953 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior allogeneic hematopoietic stem cell transplantation, solid organ transplantation disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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