ABBV-400 in Select Advanced Solid Tumor Indications

ABBV-400 in Select Advanced Solid Tumor Indications

Es posible que algunos contenidos no estén disponibles en español.

Purpose of this Study

We are doing this study to find out if an experimental drug called ABBV-400 (the study drug) is a safe and effective option for treating various types of solid tumors.

Who Can Participate?

Eligibility

Adults ages 18+ who are diagnosed with one of the following types of cancer that is advanced or metastatic:
  • Hepatocellular carcinoma (HCC); OR
  • Biliary tract cancer (BTC); OR
  • Pancreatic ductal adenocarcinoma (PDAC); OR
  • Esophageal squamous cell carcinoma (ESCC); OR
  • Triple-negative breast cancer (TNBC); OR
  • HR-positive and HER2-negative breast cancer (HR+/HER-); OR
  • Head and neck squamous cell carcinoma (HNSCC)
For more information about who can join this study, please contact the study team at gi-oncology-cru@dm.duke.edu or 919-668-1861.

What is Involved?

Description

If you choose to join this study, you will:
  • Get the study drug through an IV once every 3 weeks
  • Have a tumor biopsy done, if necessary
  • Have blood draws
  • Have imaging scans (CT or MRI)

Study Details

Full Title

A Phase 1 Open-Label Study to Evaluate the Efficacy and Safety of ABBV-400 in Select Advanced Solid Tumor Indications

Principal Investigator

John
Strickler

Protocol Number

PRO00113960

NCT ID

NCT06084481

Phase

I

Enrollment Status

Open to Enrollment