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NCT07132606

The Predictive Value of Serum Histone Succinylation in Malignant Solid Tumors

Not yet recruiting Last updated 20 August 2025
What this trial tests

trial in Malignant Tumors in 1,000 participants. Not yet recruiting.

Timeline
20 August 2025
Primary endpoint
31 December 2025
1 August 2026

Quick facts

Lead sponsorYinghua Ji
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment1,000
Start date20 August 2025
Primary completion31 December 2025
Estimated completion1 August 2026

Conditions studied

Sponsor

Yinghua Ji

Who can join

18 and older, any sex, with Malignant Tumors. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In recent years, advances in protein post-translational modification (PTM) research have revealed histone succinylation as a novel epigenetic modification mechanism critically involved in tumor initiation, progression, and prognosis. Succinylation alters protein physicochemical properties and functions, thereby modulating cellular metabolism, proliferation, and apoptosis. Aberrant histone succinylation in tumor cells demonstrates significant correlations with tumor type, staging, and clinical outcomes, offering new avenues for early cancer diagnosis. This project utilizes blood serum samples to quantify histone succinylation levels through modification-specific antibody-based detection. Integrated with clinical data, this approach enables early, rapid, and accurate pan-cancer diagnosis, achieving tumor screening via a single-tube blood test. It represents a paradigm shift in precision oncology from "gene-driven" to "epigenetic-metabolic-driven" early detection.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07132606.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing