Clinical Trials Logo

Clinical Trial Summary

The chemoradiotherapy (CCRT) is still a standard treatment for the unresectabl stage III NSCLC.However, prognosis following this treatment is generally poor, with 5-year survival of 15-20%. The result of published HELPER study had showed that Endostar, a kind of angiogenesis agent, in combination with CCRT could improve the efficacy and safety. In order to verify the rusults, the investigators design the current study.


Clinical Trial Description

The current study is a observation study in the real world setting. The 500 patients in compliance with Enrollment Criteria will be as the objects of observation. The procedure of study include the period of screening, treating and follow-up. The duration of study is about two and half year. The data entrying will be done by CRC, using the EDC system. CRA will audit the quality of data regularly. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04161352
Study type Observational
Source Zhejiang Cancer Hospital
Contact Ming Chen, Doctor
Phone 18758875572
Email chenming@zjcc.org.cn
Status Not yet recruiting
Phase
Start date November 25, 2019
Completion date December 30, 2023

See also
  Status Clinical Trial Phase
Recruiting NCT04982549 - A Study to Evaluate the Safety of Concurrent Durvalumab With CRT Followed by Durvalumab for Chinese Unresectable Stage III NSCLC Phase 2
Terminated NCT04381494 - Mobile Devices to Detect Early Pneumonitis in Stage III NSCLC Patients on Durvalumab. Phase 4