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Study identifier: NCT07155174 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study to Evaluate the Optimal Dose, Adverse Events and Change in Disease Activity of Intravenous ABBV-706 in Combination With Atezolizumab Versus Standard of Care as First-Line Treatment in Adult Participants With Previously Untreated Extensive Stage Small Cell Lung Cancer

Condition: Small Cell Lung Cancer  ·  Sponsor: AbbVie

PhasePhase 2
Planned participants180
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Small cell lung cancer (SCLC) is characterized by aggressive and rapid growth and a tendency to develop early spread to distant sites including mediastinal lymph nodes, liver, bones, adrenal glands, and brain. The purpose of this study is to assess safety, dose, change in disease activity of ABBV-706 given with atezolizumab, compared to standard of care (SOC) treatment (etoposide, carboplatin, atezolizumab, and optional lurbinectedin). ABBV-706 is an investigational drug being developed for the treatment of SCLC. There are multiple treatment arms in this study. Participants will either receive ABBV-706 given with atezolizumab, at 1 of 2 doses, or SOC. Approximately 180 adult participants will be enrolled in the study across sites worldwide. In the safety lead-in, participants with SCLC will receive intravenous (IV) ABBV-706 in 1 of 2 doses with IV atezolizumab, or IV SOC. In the expansion portion of the study, participants with SCLC will receive IV ABBV-706 in 1 of 2 doses with atezolizumab, or IV SOC, until the optimal dose of ABBV-706 is determined. The estimated duration of the study is up to 69.5 months. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic and may require frequent medical assessments, blood tests, questionnaires, and scans.

This description comes directly from the study's public registry record.

Talk to the study team

ABBVIE CALL CENTER  ·  844-663-3742  ·  abbvieclinicaltrials@abbvie.com

Always discuss trial participation with your own doctor first.

Locations (61)

Yale University School of Medicine /ID# 278181New Haven, Connecticut, United StatesRecruiting
Ocala Oncology Center /ID# 278269Ocala, Florida, United StatesRecruiting
Moffitt Cancer Center /ID# 277573Tampa, Florida, United StatesRecruiting
Fort Wayne Medical Oncology And Hematology /ID# 277336Fort Wayne, Indiana, United StatesRecruiting
Baptist Health Lexington /ID# 277729Lexington, Kentucky, United StatesRecruiting
Dana-Farber Cancer Institute /ID# 277732Boston, Massachusetts, United StatesRecruiting
Missouri Cancer Associates /ID# 278299Columbia, Missouri, United StatesRecruiting
University Hospitals Cleveland Medical Center /ID# 277556Cleveland, Ohio, United StatesRecruiting
The University of Texas MD Anderson Cancer Center /ID# 277929Houston, Texas, United StatesRecruiting
Virginia Cancer Specialists - Fairfax /ID# 278298Fairfax, Virginia, United StatesRecruiting
Grand Hopital de Charleroi - Les Viviers /ID# 276897Charleroi, Hainaut, BelgiumRecruiting
Groupe Sante CHC - Clinique du MontLegia /ID# 276783Liège, Liege, BelgiumRecruiting

+ 49 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07155174