A Study of AT13387 in Patients With Non-Small Cell Lung Cancer (NSCLC) Alone and in Combination With Crizotinib
The purpose of the study is to evaluate safety and efficacy of AT13387 Alone and in Combination with Crizotinib in the Treatment of Non-small Cell Lung Cancer.
Checked against the public recordLast updated Aug 2, 2024 · Source: ClinicalTrials.gov
What this study is about
- Purpose
- Treatment
- Study type
- Interventional
- Phase
- Phase 1 / Phase 2
- Sponsor
- Astex Pharmaceuticals, Inc.
- Interventions being studied
- Drug: AT13387; Drug: Crizotinib
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
Inclusion Criteria: 1. Men or women 18 years of age or older 2. Must have Non-small Cell Lung Cancer with ALK+ mutation or other mutations or rearrangements potentially sensitive to crizotinib 3. Measurable disease 4. Must have been receiving or have received crizotinib 5. Have adequate cardiac, bone marrow, liver and kidney function 6. Must be willing and able to provide written informed consent and comply with the protocol and study procedures Exclusion Criteria: 1. Prior anti-cancer treatment with any HSP90 inhibitor 2. Have received chemotherapy, radiation therapy or other anticancer treatment other than crizotinib within 3 weeks prior to the first dose of study drug 3. Prior malignancy other than adequately treated basal or squamous cell carcinoma of the skin, superficial bladder cancer, low-grade cervical cancer, non-metastatic prostate cancer, or have been disease-free for at least 3 years 4. Abnormal heart function 5. Presence of a life-threatening illness, medical condition, organ system dysfunction, or other factors 6. Hypersensitivity of AT13387 or other components of the drug product 7. Treatment with an investigational drug within 3 weeks prior to the first dose of study drug 8. Severe systemic diseases or active uncontrolled infections 9. Known history of human immunodeficiency virus (HIV) or seropositive test for hepatitis C virus or hepatitis B virus
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- Mayo Clinic-ScottsdaleScottsdale, Arizona
- University of California, San Diego Medical CenterLa Jolla, California
- USC Norris Comprehensive Cancer CenterLos Angeles, California
- UCLA Medical CenterLos Angeles, California
- Sharp Clinical Oncology Research-Sharp Memorial HospitalSan Diego, California
- Innovative Clinical Research InstituteWhittier, California
- University of Colorado DenverAurora, Colorado
- Yale University School of Medicine-Yale Cancer CenterNew Haven, Connecticut
- Christiana HospitalNewark, Delaware
- Florida Hospital Cancer InstituteOrlando, Florida
- H. Lee Moffitt Cancer Center & Research InstituteTampa, Florida
- Northwestern University The Feinberg School of MedicineChicago, Illinois
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Aug 2, 2024. Always confirm current availability with the study team.