Apatinib in Advanced Non-squamous,NSCLC
- Sponsor
- Jian Fang
- Study ID
- NCT03376191
- Status
- Unknown
Conditions
- Non-squamous Non-Small Cell Lung Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- apatinib — DRUGClinicians chose the initial dose of apatinib according to the patient's physical condition. Besides the clinicians adjusted the dose according to the patient's tolerance during the medication.The dosage was demanded not higher than 750 milligram (mg) per day. The patients received apatinib continuously, 28 days for a period, until intolerance, no longer getting benefits or patient wanted stop.
Study Details
To explore the efficacy and safety of apatinib in non-squamous non-small cell lung cancer in the real-world.
Key Dates
- Start date
- May 1, 2017
- Status verified
- Dec 2017
- Primary completion
- Apr 1, 2019
- Completion
- Oct 1, 2019
Study Design
- Enrollment
- 100 participants (estimated)
Primary Outcome Measure
PFS (Progression-Free survival) [ Time Frame: From the date Into this study (signed ICF) to tumor progression or death for any reason,whichever came first, assessed up to 36 months ]
Related Studies
- A Global Phase III Study of Rilvegostomig or Pembrolizumab Plus Chemotherapy for First-Line Treatment of Metastatic Non-squamous NSCLCPHASE3 · Recruiting · AstraZeneca · Mobile, Alabama
- A Study to Assess Adverse Events, Change in Disease Activity of Intravenous Telisotuzumab Adizutecan in Combination With Osimertinib as First-Line Treatment in Adult Participants With Locally Advanced Unresectable or Metastatic EGFR-Mutated Non-Squamous Non-Small Cell Lung CancerPHASE2/PHASE3 · Recruiting · AbbVie · Chandler, Arizona