Study to Assess Adverse Events and Change in Disease Activity in Adult Participants With Select Advanced Solid Tumor Indications Receiving Intravenous (IV) ABBV-400 - Join Clinical Trial NCTNCT06084481
How to Join This Clinical Trial - NCTNCT06084481
Learn how to participate in this PHASE1 trial studying an investigational therapy for Carcinoma, Breast Neoplasms, Adenocarcinoma, Carcinoma, Squamous Cell, Carcinoma, Hepatocellular, Ovarian Neoplasms, Carcinoma, Ovarian Epithelial, Triple Negative Breast Neoplasms, Squamous Cell Carcinoma of Head and Neck, Esophageal Squamous Cell Carcinoma, Biliary Tract Neoplasms. This study is currently enrolling participants.
Am I Eligible for This Clinical Trial?
This clinical research study is looking for participants with Carcinoma, Breast Neoplasms, Adenocarcinoma, Carcinoma, Squamous Cell, Carcinoma, Hepatocellular, Ovarian Neoplasms, Carcinoma, Ovarian Epithelial, Triple Negative Breast Neoplasms, Squamous Cell Carcinoma of Head and Neck, Esophageal Squamous Cell Carcinoma, Biliary Tract Neoplasms. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.
- Condition Being Studied
- Carcinoma, Breast Neoplasms, Adenocarcinoma, Carcinoma, Squamous Cell, Carcinoma, Hepatocellular, Ovarian Neoplasms, Carcinoma, Ovarian Epithelial, Triple Negative Breast Neoplasms, Squamous Cell Carcinoma of Head and Neck, Esophageal Squamous Cell Carcinoma, Biliary Tract Neoplasms
- Treatment Being Tested
- Investigational treatment
- Study Phase
- PHASE1 - Early safety study
- Enrollment Status
- Currently enrolling participants
- Study Identifier
- NCTNCT06084481 - ClinicalTrials.gov Identifier
- Sponsored By
- Study sponsor
What to Expect as a Participant
Participating in this clinical trial involves:
- Initial screening to determine eligibility
- Regular study visits and health assessments
- Receiving the study treatment or placebo
- Medical monitoring and follow-up care
- Contributing to medical research that may help others
- Potential access to new treatments before they're widely available
Clinical Trial Benefits and Compensation
Participants in this clinical research study may receive:
- Close medical monitoring by healthcare professionals
- Access to potential new treatments
- Compensation for time and travel (varies by study)
- No-cost study-related medical care
- The opportunity to help advance medical knowledge
Where Is This Clinical Trial Located?
This study is enrolling participants at 54 locations. Find a study site near you:
Clinical Research Site
Duarte, California 91010 - United States
Status: RECRUITING
Clinical Research Site
San Francisco, California 94143 - United States
Status: RECRUITING
Clinical Research Site
Aurora, Colorado 80045-7158 - United States
Status: COMPLETED
Clinical Research Site
Denver, Colorado 80218 - United States
Status: RECRUITING
Clinical Research Site
Sarasota, Florida 34232 - United States
Status: RECRUITING
Clinical Research Site
Chicago, Illinois 60611-2927 - United States
Status: RECRUITING
Clinical Research Site
Chicago, Illinois 60637 - United States
Status: RECRUITING
Clinical Research Site
Grand Rapids, Michigan 49546-7062 - United States
Status: RECRUITING
Clinical Research Site
Saint Louis, Missouri 63110 - United States
Status: RECRUITING
Clinical Research Site
New York, New York 10065-6007 - United States
Status: RECRUITING
And 44 more locations available. Contact us to find the nearest participating site.
How to Enroll in This Study
To learn more about participating in this PHASE1 clinical trial for Carcinoma, Breast Neoplasms, Adenocarcinoma, Carcinoma, Squamous Cell, Carcinoma, Hepatocellular, Ovarian Neoplasms, Carcinoma, Ovarian Epithelial, Triple Negative Breast Neoplasms, Squamous Cell Carcinoma of Head and Neck, Esophageal Squamous Cell Carcinoma, Biliary Tract Neoplasms:
- Review the eligibility criteria with your healthcare provider
- Contact the study team for a pre-screening interview
- Schedule an in-person screening visit if eligible
- Review and sign the informed consent form
- Begin participation in the clinical trial
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