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Clinical Trials in China / NCT05667948
Recruiting Observational

Molecular Analysis and Treatment Options of Thymic Malignancies

NCT05667948 · tracked via the Priya Life Science China tracker
Sponsor
Shanghai Chest Hospital
Phase
Observational
Started
2016-01-01
Last updated
2025-05-22

Condition(s) studied

Thymic Epithelial TumorThymic CarcinomaThymic Cancer

Investigational drug(s) / intervention(s)

Chemotherapy

Chemotherapy: different treatments based on the molecular analysis

Study summary

Thymic malignancies are the most common tumors of the anterior mediastinum, though surgery and radiation often effectively treat thymic carcinomas, a minority continue to progress and eventually lead to death. Therefore, there is an unmet need for more effective therapies for thymic malignancies. Considering the role of molecular alterations has yet to be defined in the treatment of thymoma and thymic malignancies, there is an urgent recognition that molecular alterations in the thymic malignancies are important to predict response and survival for novel targeted therapies.

In summary, identification of genetic alterations in thymic malignancies is increasingly essential to perform molecular diagnostics and individualized treatments. This project aims to create a registry of patients with thymic malignancies to further the characterization of molecular alterations and develop (novel) treatments based on the detection.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Histologically proven diagnosis of thymic malignancies * 18 years of age or older * Ability to understand and the willingness to sign a written informed consent document

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Xiaomin Niu Shanghai Shanghai Municipality Recruiting

More Shanghai Chest Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05667948 on ClinicalTrials.gov ↗ ← All trials in China