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RECRUITING
NCT06628310
PHASE2

A Study to Evaluate the Adverse Events, Efficacy, and Optimal Dose of Intravenous (IV) ABBV-400 in Combination With IV Fluorouracil, Leucovorin, and Budigalimab in Adult Participants With Locally Advanced Unresectable or Metastatic Gastric, Gastroesophageal Junction, or Esophageal Adenocarcinoma

Sponsor: AbbVie

View on ClinicalTrials.gov

Summary

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 telisotuzumab adizutecan (ABBV-400) is given in combination with Fluorouracil, Leucovorin, and a programmed cell death receptor 1 (PD1) inhibitor Budigalimab. The combination (AFLB) will be given to adult participants to treat locally advanced unresectable or metastatic gastric, gastroesophageal junction, or esophageal adenocarcinoma (mGEA). Telisotuzumab Adizutecan (ABBV-400) and Budigalimab are investigational drugs being developed for the treatment of mGEA. Fluorouracil and Leucovorin are drugs approved for the treatment of mGEA. This study will be divided into two stages, with the first stage treating participants with increasing doses of ABBV-400 within the AFLB regimen until the dose reached is tolerable and expected to be efficacious. Participants will then be randomized into groups called treatment arms where one group will receive Budigalimab and FOLFOX (Fluorouracil, Leucovorin, and Oxaliplatin) . A further two treatment groups will receive AFLB, but with two optimized doses of ABBV-400 to allow for the best dose to be studied in the future. Approximately 180 adult participants with mGEA will be enrolled in the study in 51 sites worldwide. In the dose escalation stage, participants will be treated with increasing intravenous (IV) doses of telisotuzumab adizutecan (ABBV-400) within the AFLB regimen until the dose reached is tolerable and expected to be efficacious. In the dose optimization stage, participants will receive FOLFOX or receive AFLB, but with one of two optimized doses of ABBV-400. The study will run for a duration of approximately 6 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.

Official title: A Phase 2 Randomized Study to Evaluate the Safety, Efficacy, and Optimal Dose of Telisotuzumab Adizutecan in Combination With Fluorouracil, Leucovorin, and Budigalimab as First-Line Treatment in Subjects With Locally Advanced Unresectable or Metastatic Gastric, Gastroesophageal Junction, or Esophageal Adenocarcinoma (AndroMETa-GEA-977)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

180

Start Date

2024-12-13

Completion Date

2030-10

Last Updated

2026-03-30

Healthy Volunteers

No

Interventions

DRUG

Telisotuzumab Adizutecan

Intravenous (IV) Infusion

DRUG

Budigalimab

IV Infusion

DRUG

Fluorouracil

IV Infusion; IV Injection

DRUG

Leucovorin

IV Infusion; IV Injection

DRUG

Oxaliplatin

IV Infusion

Locations (49)

City of Hope National Medical Center /ID# 268690

Duarte, California, United States

City of Hope - Orange County Lennar Foundation Cancer Center /ID# 272630

Irvine, California, United States

UCLA - Santa Monica /ID# 270024

Santa Monica, California, United States

AdventHealth Orlando /ID# 268561

Orlando, Florida, United States

City Of Hope - Atlanta. /ID# 280646

Newnan, Georgia, United States

Hattiesburg Clinic /ID# 268572

Hattiesburg, Mississippi, United States

Duke University Medical Center /ID# 268186

Durham, North Carolina, United States

Millennium Research & Clinical Development /ID# 268540

Houston, Texas, United States

Algemeen Ziekenhuis klina /ID# 268754

Brasschaat, Antwerpen, Belgium

Universitair Ziekenhuis Leuven /ID# 269957

Leuven, Vlaams-Brabant, Belgium

CHU de Liege /ID# 270223

Liège, Belgium

Princess Margaret Cancer Centre /ID# 268277

Toronto, Ontario, Canada

Centre Hospitalier de l'Universite de Montreal (CHUM) /ID# 268763

Montreal, Quebec, Canada

Jewish General Hospital /ID# 268413

Montreal, Quebec, Canada

Beijing Cancer Hospital /ID# 268455

Beijing, Beijing Municipality, China

Cancer Hospital Chinese Academy of Medical Sciences(Langfang) /ID# 277479

Langfang, Hebei, China

Harbin Medical University Cancer Hospital /ID# 268452

Harbin, Heilongjiang, China

Union Hospital - Tongji Medical College /ID# 268796

Wuhan, Hubei, China

The first Affiliated Hospital, Zhejiang University School of Medicine. /ID# 268782

Hangzhou, Zhejiang, China

Universitaetsklinikum Freiburg /ID# 270407

Freiburg im Breisgau, Baden-Wurttemberg, Germany

TUM Klinikum rechts der Isar /ID# 267792

Munich, Bavaria, Germany

Krankenhaus Nordwest /ID# 268462

Frankfurt am Main, Hesse, Germany

Universitaetsklinikum Leipzig /ID# 270432

Leipzig, Saxony, Germany

Haematologisch-Onkologische Praxis Eppendorf /ID# 268024

Hamburg, Germany

Meir Medical Center /ID# 267998

Kfar Saba, Central District, Israel

Soroka Medical Center /ID# 268301

Beersheba, Southern District, Israel

Tel Aviv Sourasky Medical Center /ID# 267755

Tel Aviv, Tel Aviv, Israel

Shaare Zedek Medical Center /ID# 267752

Jerusalem, Israel

Hadassah Medical Center-Hebrew University /ID# 267753

Jerusalem, Israel

Aichi Cancer Center /ID# 268124

Nagoya, Aichi-ken, Japan

National Cancer Center Hospital East /ID# 268083

Kashiwa-shi, Chiba, Japan

Shizuoka Cancer Center /ID# 268123

Sunto-gun, Shizuoka, Japan

National Cancer Center Hospital /ID# 268648

Chuo-Ku, Tokyo, Japan

The Cancer Institute Hospital Of JFCR /ID# 268656

Koto-ku, Tokyo, Japan

Pan American Center for Oncology Trials /ID# 268833

Rio Piedras, Puerto Rico

Hospital Universitario de Navarra /ID# 270119

Pamplona, Navarre, Spain

Hospital General Universitario Gregorio Maranon /ID# 270037

Madrid, Spain

Complexo Hospitalario Universitario de Ourense /ID# 270042

Ourense, Spain

Hospital Clinico Universitario de Valencia /ID# 270040

Valencia, Spain

Kaohsiung Medical University Chung-Ho Memorial Hospital /ID# 267672

Kaohsiung City, Taiwan

China Medical University Hospital /ID# 267667

Taichung, Taiwan

National Cheng Kung University Hospital /ID# 267669

Tainan, Taiwan

National Taiwan University Hospital /ID# 267666

Taipei, Taiwan

Taipei Veterans General Hospital /ID# 267664

Taipei, Taiwan

Linkou Chang Gung Memorial Hospital /ID# 267668

Taoyuan, Taiwan

Barts Health NHS Trust /ID# 270796

London, Greater London, United Kingdom

Oxford University Hospital NHS Trust /ID# 274614

Oxford, Oxfordshire, United Kingdom

Queen Elizabeth Hospital Birmingham /ID# 271199

Birmingham, United Kingdom

NHS Tayside Health Board /ID# 270799

Dundee, United Kingdom