ClinicalTrials.gov record
Active, not recruiting Phase 1 Interventional

A Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of ABBV-927 With ABBV-368, Budigalimab (ABBV-181) and/or Chemotherapy in Participants With Locally Advanced or Metastatic Solid Tumors

ClinicalTrials.gov ID: NCT03893955

Public ClinicalTrials.gov record NCT03893955. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 5, 2026, 11:05 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1, Multicenter, Open-Label Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of Combinations of ABBV-927 With ABBV-368, Budigalimab (ABBV-181) and/or Chemotherapy in Subjects With Locally Advanced or Metastatic Solid Tumors

Study identification

NCT ID
NCT03893955
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
AbbVie
Industry
Enrollment
150 participants

Conditions and interventions

Interventions

  • ABBV-181 Drug
  • ABBV-368 Drug
  • ABBV-927 Drug
  • Carboplatin Drug
  • Nab-paclitaxel Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 20, 2019
Primary completion
Feb 28, 2026
Completion
Feb 28, 2026
Last update posted
Aug 11, 2025

2019 – 2026

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
Highlands Oncology Group, PA /ID# 218863 Springdale Arkansas 72762
St Jude Hospital dba St Joseph /ID# 211130 Santa Rosa California 95403
Yale University School of Medicine /ID# 210678 New Haven Connecticut 06510
Moffitt Cancer Center /ID# 215037 Tampa Florida 33612-9416
Fort Wayne Medical Oncology and Hematology, Inc /ID# 226072 Fort Wayne Indiana 46804
Washington University-School of Medicine /ID# 221399 St Louis Missouri 63110
Duke Cancer Center /ID# 217641 Durham North Carolina 27710-3000
Carolina BioOncology Institute /ID# 210664 Huntersville North Carolina 28078
UPMC Hillman Cancer Ctr /ID# 222747 Pittsburgh Pennsylvania 15232
Tennessee Oncology-Nashville Centennial /ID# 221400 Nashville Tennessee 37203-1632
Mary Crowley Cancer Research /ID# 210716 Dallas Texas 75230
NEXT Oncology /ID# 210717 San Antonio Texas 78229
Virginia Cancer Specialists - Fairfax /ID# 210671 Fairfax Virginia 22031

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 13 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03893955, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 11, 2025 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03893955 live on ClinicalTrials.gov.

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