Study to Assess Adverse Events and Change in Disease Activity in Adult Participants With Select Advanced Solid Tumor Indications Receiving Intravenous (IV) ABBV-400

Running, not enrolling · Phase 1

Conditions studied: Hepatocellular Carcinoma, Pancreatic Ductal Adenocarcinoma, Biliary Tract Cancers, Esophageal Squamous Cell Carcinoma, Triple Negative Breast Cancer, Hormone Receptor+/Human Epidermal Growth Factor Receptor 2 Negative Breast Cancer, Head and Neck Squamous-Cell Carcinoma, Platinum Resistant High Grade Epithelial Ovarian Cancer

In brief

Cancer is a condition where cells in a specific part of body grow and reproduce uncontrollably. The purpose of this study is to assess adverse events and change in disease activity when ABBV-400 is given to adult participants to treat advanced solid tumors. ABBV-400 is an investigational drug being developed for the treatment of advanced solid tumors. Study doctors put the participants in groups called cohorts. Cohorts 1-8 receive ABBV-400 alone (monotherapy), cohort 9 receives ABBV-400 with a strong CYP3A3 inhibitor (ITZ), and cohort 10 receives ABBV-400 with bevacizumab. All cohorts are followed by a safety follow-up period. Approximately 325 adult participants with hepatocellular carcinoma (HCC), pancreatic ductal adenocarcinoma (PDAC), biliary tract cancers (BTC), esophageal squamous cell carcinoma (ESCC), triple negative breast cancer (TNBC), hormone receptor+/human epidermal growth factor receptor 2 negative (HER2-) breast cancer (hormone receptor-positive \[HR+\]/HER2-breast cancer \[BC\]), head and neck squamous-cell-carcinoma (HNSCC), Platinum Resistant High Grade Epithelial Ovarian Cancer (PROC)/primary peritoneal/fallopian tube cancer, or advanced solid tumors, will be enrolled in the study in approximately 54 sites worldwide. In cohorts 1-8, participants with the following advanced solid tumor indications: HCC, PDAC, BTC, ESCC, TNBC, HR+/HER2-BC, HNSCC, and PROC/primary peritoneal/fallopian tube cancer will receive intravenous (IV) ABBV-400 monotherapy, in cohort 9 participants will receive IV ABBV-400 and an oral solution of ITZ, and in cohort 10 participants will receive IV ABBV-400 and IV bevacizumab, for up to 3 years during and up to the treatment period with an additional safety follow-up period of up to 2 years. 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 an approved institution (hospital or clinic). The effect of the treatment will be frequently checked by medical assessments, blood tests, questionnaires and side effects.

Key facts

Study ID

NCT06084481

Run by

AbbVie

People needed

302

Starts

2023-11-09

Expected to finish

2027-09-01

Last updated by the study team

2026-08-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Laboratory values meeting the criteria laid out in the protocol.
• Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
• Documented diagnosis of locally advanced or metastatic hepatocellular carcinoma (HCC), pancreatic ductal adenocarcinoma (PDAC), biliary tract cancers (BTC), squamous cell carcinoma of the esophagus, (ESCC), triple negative breast cancer (TNBC), hormone receptor+/HER2-breast cancer (HR+/HER2-BC), head and neck squamous-cell-carcinoma (HNSCC), or Platinum Resistant High Grade Epithelial Ovarian Cancer (PROC)/primary peritoneal/fallopian tube cancer (by World Health Organization [WHO] criteria). Participant meets the criteria for disease activity laid out in the protocol.

You may not qualify if…

• Have received anticancer therapy including chemotherapy, radiation therapy, immunotherapy, biologic, or any investigational therapy within 28 days or 5 half-lives of the drug (whichever is shorter) prior to the first dose of ABBV-400. Palliative radiation therapy for bone, skin, or subcutaneous metastases with 10 fractions or less is permitted and not subject to a washout period.
• Unresolved clinically significant AEs > Grade 1 from prior anticancer therapy.
• History of interstitial lung disease (ILD) or pneumonitis that required treatment with systemic steroids, or any evidence of active ILD or pneumonitis, including but not limited to those listed in the protocol.
• History of clinically significant, intercurrent lung-specific illnesses, including those laid out in the protocol.
• Untreated brain or meningeal metastases (i.e., participants with history of metastases are eligible provided they do not require ongoing steroid treatment for cerebral edema and have shown clinical and radiographic stability for at least 14 days after definitive therapy). Participants may continue on antiepileptic therapy if required.
• History of other active malignancy, with the exception of those laid out in the protocol.
• Any autoimmune, connective tissue or inflammatory disorders with documented or suspicious pulmonary involvement at screening (i.e., rheumatoid arthritis, Sjogren's, sarcoidosis etc.), and prior pneumonectomy.

Where it is running

• Univ Hosp Cleveland /ID# 257706 — Cleveland, Ohio, United States
• Lifespan Cancer Institute at Rhode Island Hospital /ID# 257693 — Providence, Rhode Island, United States
• MUSC Hollings Cancer Center /ID# 257935 — Charleston, South Carolina, United States
• Prisma Health /ID# 257697 — Greenville, South Carolina, United States
• Tennessee Oncology-Nashville Centennial /ID# 261568 — Nashville, Tennessee, United States
• MD Anderson Cancer Center /ID# 255131 — Houston, Texas, United States
• Univ Texas HSC San Antonio /ID# 257708 — San Antonio, Texas, United States
• South Texas Accelerated Research Therapeutics /ID# 260404 — San Antonio, Texas, United States
• Inova Schar Cancer Institute - Fairfax - Innovation Park Drive /ID# 262771 — Fairfax, Virginia, United States
• Chris O'Brien Lifehouse /ID# 262765 — Camperdown, New South Wales, Australia
• Austin Health /ID# 256635 — Heidelberg, Victoria, Australia
• Rabin Medical Center. /ID# 256650 — Petah Tikva, Central District, Israel
• The Chaim Sheba Medical Center /ID# 255731 — Ramat Gan, Tel Aviv, Israel
• Tel Aviv Sourasky Medical Center /ID# 258931 — Tel Aviv, Tel Aviv, Israel
• Rambam Health Care Campus /ID# 256649 — Haifa, Israel
• Hadassah Medical Center-Hebrew University /ID# 256655 — Jerusalem, Israel
• NHO Nagoya Medical Center /ID# 261001 — Nagoya, Aichi-ken, Japan
• Aichi Cancer Center Hospital /ID# 256679 — Nagoya, Aichi-ken, Japan
• National Cancer Center Hospital East /ID# 258934 — Kashiwa-shi, Chiba, Japan
• Kyoto University Hospital /ID# 256680 — Kyoto, Kyoto, Japan
• Shizuoka Cancer Center /ID# 257789 — Sunto-gun, Shizuoka, Japan
• National Cancer Center Hospital /ID# 261136 — Chuo-Ku, Tokyo, Japan
• The Cancer Institute Hospital Of JFCR /ID# 257788 — Koto-ku, Tokyo, Japan
• Pan American Center for Oncology Trials - Rio Piedras /ID# 262903 — Rio Piedras, Puerto Rico
• Duke Cancer Center /ID# 255129 — Durham, North Carolina, United States

Full record on ClinicalTrials.gov

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