Actively Recruiting

Phase 2
Phase 3
Age: 18Years +
All Genders
NCT04322617

Anlotinib Plus Immune Checkpoint Inhibitors for Lung Cancer

Led by Hunan Province Tumor Hospital · Updated on 2024-06-04

1200

Participants Needed

1

Research Sites

469 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to explore the efficacy of Anlotinib with or without Immune Checkpoint Inhibitor in Standard Chemo-immunotherapy Failed Advanced NSCLC.

CONDITIONS

Official Title

Anlotinib Plus Immune Checkpoint Inhibitors for Lung Cancer

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Understand and agree to the clinical trial by signing informed consent
  • Age 18 years or older
  • Confirmed diagnosis of lung cancer by tissue or cell analysis
  • Have failed first-line chemo-immunotherapy treatment
  • ECOG performance status score of 0 or 1
  • Predicted survival time of at least 12 weeks
  • Adequate bone marrow and organ function
  • Presence of measurable tumors based on RECIST 1.1 criteria
  • Stable brain metastases allowed
Not Eligible

You will not qualify if you...

  • Received EGFR or VEGFR antibody treatments within 4 weeks before starting study drug
  • Radiation therapy within 14 days before study drug start, or ongoing radiation toxicity
  • Use of strong CYP1A2 or CYP3A inhibitors or inducers within 1-2 weeks before starting study drug
  • Spinal cord compression or meningeal metastasis
  • History of other cancers within the past 2 years
  • Severe side effects (above grade 1) from prior treatments
  • Stroke or brain bleeding within 6 months before study drug start
  • Severe or uncontrolled systemic diseases including hypertension and active bleeding
  • Active infections including hepatitis B, hepatitis C, HIV, or COVID-19
  • Heart diseases or abnormalities
  • History of interstitial lung disease or immune-related pneumonia
  • Severe nausea, vomiting, swallowing difficulties, or absorption problems
  • Live vaccines given within 2 weeks before starting study drug
  • Pregnant or breastfeeding women
  • Allergy to study drugs or their ingredients
  • Other conditions that make participation unsuitable as judged by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Yongchang Zhang

Changsha, Hunan, China, 410013

Actively Recruiting

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Research Team

Y

Yongchang Zhang, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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