Actively Recruiting

Phase 2
Age: 18Years +
All Genders
NCT05363280

Phase 2 Study for the Patient, Who Has Diagnosed With Small Cell Lung Cancer (SCLC) or Non Small Cell Lung Cancer (NSCLC) or Renal Cell Carcinoma (RCC) and Finished the First Line Stand Treatment , Need More Treatment

Led by Advenchen Pharmaceuticals, LLC. · Updated on 2026-05-08

80

Participants Needed

7

Research Sites

317 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This trial is a Phase II trial designed to evaluate the safety and efficacy of using oral AL8326 , a multi-targeted receptor Tyrosine Kinase Inhibitor( TKI) , to recurrent, advanced, or metastatic small cell lung cancer (SCLC) patients , Non-Small Cell Lung (NSCLC) and Renal Cell Carcinoma patients who need ≥2nd line treatment .

CONDITIONS

Official Title

Phase 2 Study for the Patient, Who Has Diagnosed With Small Cell Lung Cancer (SCLC) or Non Small Cell Lung Cancer (NSCLC) or Renal Cell Carcinoma (RCC) and Finished the First Line Stand Treatment , Need More Treatment

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female, 18 years of age or older
  • ECOG performance status of 0 or 1
  • Histologically or cytologically confirmed small cell lung cancer, non-small cell lung cancer, or renal cell carcinoma
  • At least one measurable lesion according to RECIST 1.1 criteria
  • Life expectancy of at least 3 months
Not Eligible

You will not qualify if you...

  • Serious, non-healing wound, ulcer, or bone fracture
  • Major surgery within 28 days or minor surgery within 7 days before treatment
  • Active bleeding or high risk of bleeding conditions like bleeding disorders or tumors involving major vessels
  • Significant cardiovascular disease including uncontrolled hypertension, recent heart attack or unstable angina within 6 months, severe heart failure, serious arrhythmia needing medication, or severe peripheral vascular disease
  • Hemoptysis within 3 months before enrollment
  • Use of strong CYP3A4, CYP2C9, or CYP2C19 inhibitors or inducers within 14 days before enrollment and during the study unless medically necessary

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 7 locations

1

University of Alabama at Birmingham

Birmingham, Alabama, United States, 35294

Actively Recruiting

2

Cleveland Clinic Florida

Weston, Florida, United States, 33331

Withdrawn

3

Northwestern University

Chicago, Illinois, United States, 60611

Completed

4

Siteman Cancer Center, Washington University

St Louis, Missouri, United States, 63130

Actively Recruiting

5

Cleveland Clinic

Cleveland, Ohio, United States, 44195

Actively Recruiting

6

Hospital Universitari Vall d'Hebron

Barcelona, Spain

Actively Recruiting

7

Hospital Universitario Ramón Y Cajal

Madrid, Spain

Actively Recruiting

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Research Team

S

Shiying Sprinzl

CONTACT

J

Judy Chen

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

5

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Phase 2 Study for the Patient, Who Has Diagnosed With Small Cell Lung Cancer (SCLC) or Non Small Cell Lung Cancer (NSCLC) or Renal Cell Carcinoma (RCC) and Finished the First Line Stand Treatment , Need More Treatment | DecenTrialz