TERMINATED

A Study to Assess the Safety, Pharmacokinetics, and Efficacy of Intravenous (IV) ABBV-303, as Monotherapy and in Combination With IV Infused Budigalimab (ABBV-181), in Adults With Advanced Solid Tumors

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Cancer is a condition where cells in a specific part of body grow and reproduce uncontrollably. The purpose of this study is to assess safety, tolerability, pharmacokinetics and preliminary efficacy of ABBV-303 as a monotherapy and in combination with budigalimab, (ABBV-181). ABBV-303 is an investigational drug being developed for the treatment of solid tumors. There are multiple treatment arms in this study. Participants will either receive ABBV-303 as a single agent or in combination with budigalimab (another investigational drug) at different doses. Approximately 181 adult participants will be enrolled in the study across sites worldwide. In Part A, ABBV-303 will be intravenously (IV) infused in escalating doses as a monotherapy in participants with relapsed (R)/refractory (R) solid tumors, R/R non-small cell lung cancer (NSCLC), R/R renal cell carcinoma (RCC), R/R head and neck squamous cell carcinoma (HNSCC), or R/R tissue agnostic participants with mesenchymal epithelial transition. In Part B, ABBV-303 in combination with budigalimab will be IV infused in participants with R/R solid tumors or NSCLC. The estimated duration of the study is up to 3 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 a hospital or clinic and may require frequent medical assessments, blood tests, and scans.

Official Title

A Phase 1 First-in-Human, Open-Label Study Evaluating the Safety, Pharmacokinetics, and Efficacy of ABBV-303, as Monotherapy and in Combination With Budigalimab (ABBV-181), in Adult Subjects With Advanced Solid Tumors

Quick Facts

Study Start:2024-02-06
Study Completion:2025-10-22
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:TERMINATED

Study ID

NCT06158958

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Participants with Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  2. * Laboratory values meeting the protocol's criteria within the screening period (-28 days) prior to the first dose of study drug.
  3. * Participants with a diagnosis of a malignant solid tumor by histology (World Health Organization \[WHO\] criteria).
  4. * Participants with measurable disease per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1).
  1. * Unresolved Grade \> 1 adverse events (AEs) from prior anti-cancer therapy except for alopecia.
  2. * Active systemic or uncontrolled local bacterial, fungal, or viral infection requiring antimicrobial therapy.
  3. * History of hypersensitivity to the active ingredients or any excipients of ABBV-303 and budigalimab (ABBV-181).
  4. * Body weight \< 35 kg.

Contacts and Locations

Principal Investigator

ABBVIE INC.
STUDY_DIRECTOR
AbbVie

Study Locations (Sites)

City of Hope /ID# 254303
Duarte, California, 91010
United States
City of Hope - Orange County Lennar Foundation Cancer Center /ID# 266792
Irvine, California, 92618
United States
University of Southern California /ID# 254356
Los Angeles, California, 90033
United States
START Midwest /ID# 256945
Grand Rapids, Michigan, 49546-7062
United States
Washington University-School of Medicine /ID# 262943
St Louis, Missouri, 63110
United States
NYU Langone - Laura and Isaac Perlmutter Cancer Center /ID# 256943
New York, New York, 10016
United States
Carolina BioOncology Institute /ID# 254305
Huntersville, North Carolina, 28078
United States
The Ohio State University - The James /ID# 260475
Columbus, Ohio, 43210-1240
United States
University of Texas MD Anderson Cancer Center /ID# 254308
Houston, Texas, 77030
United States
NEXT Oncology /ID# 257395
San Antonio, Texas, 78229
United States
South Texas Accelerated Research Therapeutics /ID# 256944
San Antonio, Texas, 78229
United States

Collaborators and Investigators

Sponsor: AbbVie

  • ABBVIE INC., STUDY_DIRECTOR, AbbVie

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-06
Study Completion Date2025-10-22

Study Record Updates

Study Start Date2024-02-06
Study Completion Date2025-10-22

Terms related to this study

Keywords Provided by Researchers

  • Solid Tumors
  • Non-Small Cell Lung Cancer
  • NSCLC
  • Renal Cell Carcinoma
  • RCC
  • Head and Neck Squamous Cell Carcinoma
  • HNSCC
  • ABBV-303
  • ABBV-181
  • Budigalimab

Additional Relevant MeSH Terms

  • Solid Tumors