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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06174857
Other study ID # EGFR 19 delins
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2021
Est. completion date September 15, 2025

Study information

Verified date December 2023
Source Hunan Province Tumor Hospital
Contact Yongchang C Zhang, MD
Phone +8613873123436
Email zhangyongchang@csu.edu.cn
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This is a descriptive observational study, in which data are collected in an epidemiological fashion and prospective. This study does not intend to intervene the current medical practice of the recruited patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date September 15, 2025
Est. primary completion date June 15, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients must be =18 years. - Provision of fully informed consent prior to any study specific procedures. - Advanced or metastatic lung squamous cell carcinoma confirmed by histology or cytology. - According to the RECIST 1.1 standard, the patient must have at least one measurable lesion. Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Hunan Cancer hospital Changsha Hunan

Sponsors (1)

Lead Sponsor Collaborator
Hunan Province Tumor Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary progression-free survival From registration onto that step until death, or censored at the date of last contact. 3 years
Primary Overall survival From registration onto that step until death, or censored at the date of last contact. 3 years
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