Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06352008

To Evaluate the Efficacy and Safety of Anlotinib Hydrochloride Capsule in Postoperative Non-pCR Patients With Non-small Cell Lung Cancer

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
64 (estimated)
Sponsor
Tianjin Medical University Cancer Institute and Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To explore the effectiveness of anlotinib hydrochloride capsule in postoperative non-pCR non-small cell lung cancer patients with adjuvant intensive therapy

Conditions

Interventions

TypeNameDescription
DRUGAnlotinib12mg once a day, taken orally before breakfast for 2 consecutive weeks and stopped for 1 week. Without special circumstances, it is recommended to take at a fixed time every day; If there is a missing dose during the administration, confirm that the time before the next administration is less than 12 hours, no more refilling. The maximum duration of drug use is tentatively 1 year.

Timeline

Start date
2024-07-01
Primary completion
2026-06-01
Completion
2027-06-01
First posted
2024-04-08
Last updated
2025-11-20

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06352008. Inclusion in this directory is not an endorsement.