Study Comparing Tarlatamab, Durvalumab, Carboplatin, and Etoposide with Durvalumab, Carboplatin, and Etoposide for First-line Treatment of Extensive Stage Small-Cell Lung Cancer
Sponsor: Amgen
Sponsor score: 60
ClinicalTrials ID:NCT07005128
This clinical trial is evaluating whether adding the drug tarlatamab to the standard treatment of durvalumab, carboplatin, and etoposide can help patients with extensive stage small-cell lung cancer live longer.
Patient Parameters
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Program Overview
The purpose of this study is to find out if adding tarlatamab to the usual treatment of durvalumab, carboplatin, and etoposide can improve overall survival in patients with extensive stage small-cell lung cancer (ES-SCLC). The study will compare the effectiveness of the two treatment combinations to see which one helps patients live longer.
Eligibility Criteria
Inclusion Criteria
- Must provide informed consent before starting any study-related activities.
- Must be 18 years or older, or the legal age in your country if it's higher than 18.
- Must have a confirmed diagnosis of extensive stage small-cell lung cancer (ES-SCLC) based on specific medical criteria.
- Must have measurable cancer as defined by standard criteria.
- Must be suitable to receive the combination of carboplatin, etoposide, and durvalumab as the first treatment option, according to the doctor's assessment.
- Must have a life expectancy of at least 12 weeks.
Exclusion Criteria
- Cannot have had any other cancer in the last 2 years.
- Cannot have cancer that has spread to the brain or the membranes surrounding the brain and spinal cord.
- Cannot have had severe or life-threatening reactions to immune therapy in the past.
- Cannot have had a stroke or mini-stroke within 6 months before starting the study treatment.
- Cannot have active autoimmune or inflammatory diseases.
- Cannot have active HIV or Hepatitis B or C infections.
- Cannot have lung diseases like interstitial lung disease or non-infectious pneumonitis.
- Cannot have had a solid organ transplant.
- Cannot have had a heart attack or severe heart failure within 6 months before starting the study treatment.
Locations
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| Saint Bernards Medical Center | 72401 | Jonesboro | Arkansas |
| University of Illinois Chicago | 60612 | Chicago | Illinois |
| Cancer Center of Kansas, Heritage Plaza Medical Building | 67214 | Wichita | Kansas |
| Allina Health System dba Allina Health Cancer Institute | 55407 | Minneapolis | Minnesota |
| Kaiser Permanente Medical Center | 97227 | Portland | Oregon |
| Baptist Cancer Center | 38120 | Memphis | Tennessee |
| West Virginia University Health Sciences Center | 26506 | Morgantown | West Virginia |
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