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Completed Phase 1 Interventional

A Study With ABBV-155 Alone and in Combination With Taxane Therapy in Adults With Relapsed and/or Refractory Solid Tumors

ClinicalTrials.gov ID: NCT03595059

Public ClinicalTrials.gov record NCT03595059. 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 Oct 18, 2026, 5:08 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 First-in-Human Study With ABBV-155 Alone and in Combination With Taxane Therapy in Adults With Relapsed and/or Refractory Solid Tumors

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

An open-label, dose-escalation (Part 1), dose-expansion (Part 2) study to assess the safety, pharmacokinetics (PK), and preliminary efficacy of ABBV-155 alone and in combination with paclitaxel or docetaxel. In Part 1 (dose escalation), participants will receive escalating doses of ABBV-155 monotherapy (Part 1a) or ABBV-155 in combination with paclitaxel or docetaxel (Part 1b). In Part 2 (dose expansion), participants will receive ABBV-155 monotherapy or in combination therapy. The ABBV-155 monotherapy cohort will enroll participants with relapsed or refractory (R/R) small cell lung cancer (SCLC) (Part 2a); the ABBV-155 plus a taxane (paclitaxel or docetaxel) combination cohort will enroll participants with R/R non-small cell lung cancer (NSCLC) and breast cancer (Part 2b).

Study identification

NCT ID
NCT03595059
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
AbbVie
Industry
Enrollment
168 participants

Conditions and interventions

Interventions

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
Jul 13, 2018 (Actual)
Primary completion
Sep 12, 2025 (Actual)
Completion
Sep 12, 2025 (Actual)
Last update posted
Dec 10, 2025

2018 – 2025

United States locations

U.S. sites
21
U.S. states
17
U.S. cities
20
Facility City State ZIP Site status
University of Alabama at Birmingham - Main /ID# 214024 Birmingham Alabama 35233 —
Highlands Oncology Group, PA /ID# 201568 Springdale Arkansas 72762 —
UC Irvine Medical Center - Chao Family Comprehensive Cancer Center /ID# 206105 Orange California 92868-3201 —
Duplicate_Cedars-Sinai Medical Center-West Hollywood /ID# 204267 West Hollywood California 90048 —
Univ of Colorado Cancer Center /ID# 208365 Aurora Colorado 80045 —
Yale University, Yale Cancer Center /ID# 201542 New Haven Connecticut 06510-3206 —
AdventHealth Orlando /ID# 227242 Orlando Florida 32803 —
Northwestern University Feinberg School of Medicine /ID# 201563 Chicago Illinois 60611-2927 —
Duplicate_Johns Hopkins Bayview Med Cnt /ID# 215095 Baltimore Maryland 21224 —
Johns Hopkins Hospital /ID# 201320 Baltimore Maryland 21287 —
Dana-Farber Cancer Institute /ID# 201564 Boston Massachusetts 02215 —
Duplicate_Henry Ford Hospital /ID# 226852 Detroit Michigan 48202 —
Northwell Health - Marcus Ave /ID# 204376 New Hyde Park New York 11042-2060 —
Carolina BioOncology Institute /ID# 201577 Huntersville North Carolina 28078 —
Univ Hosp Cleveland /ID# 201567 Cleveland Ohio 44106 —
University of Oklahoma, Stephenson Cancer Center /ID# 206820 Oklahoma City Oklahoma 73104-5418 —
Lifespan Cancer Institute at Rhode Island Hospital /ID# 204256 Providence Rhode Island 02903-4923 —
Vanderbilt Ingram Cancer Center /ID# 201575 Nashville Tennessee 37232-0021 —
Mary Crowley Cancer Research /ID# 214168 Dallas Texas 75230 —
MD Anderson Cancer Center /ID# 201558 Houston Texas 77030 —
NEXT Oncology /ID# 204893 San Antonio Texas 78229 —

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 19 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03595059, 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 Dec 10, 2025 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03595059 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →