Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

ACTIVE NOT RECRUITING Phase 1

A Study Evaluating the Safety, Pharmacokinetics (PK), and Preliminary Efficacy of ABBV-399 in Participants With Advanced Solid Tumors

NCT02099058 · View on ClinicalTrials.gov ↗

Study Summary

This is a Phase 1/1b open-label study evaluating the safety, pharmacokinetics (PK), and preliminary efficacy of ABBV-399 as monotherapy and in combination with osimertinib, erlotinib, and nivolumab in participants with advanced solid tumors likely to express c-Met. Enrollment is closed for the monotherapy arms, Arm A, and Arm D.

Interventions

  • DRUG Osimertinib
  • DRUG Nivolumab
  • DRUG Erlotinib
  • DRUG Telisotuzumab vedotin

Study Locations (20)

California

  • City of Hope /ID# 153759 — Duarte
  • University of California, Los Angeles /ID# 148295 — Los Angeles
  • UC Irvine /ID# 165107 — Orange
  • University of California, Davis Comprehensive Cancer Center /ID# 129805 — Sacramento

Illinois

  • The University of Chicago Medical Center /ID# 136995 — Chicago
  • Ingalls Memorial Hosp /ID# 165876 — Harvey

Massachusetts

  • Massachusetts General Hospital /ID# 129804 — Boston
  • Dana-Farber Cancer Institute /ID# 168782 — Boston

Michigan

  • Duplicate_Henry Ford Health System /ID# 149857 — Detroit
  • Herbert Herman Cancer Center /ID# 149858 — Lansing

New York

  • Northwell Health - Monter Cancer Center /ID# 218170 — Lake Success
  • Montefiore Medical Park at Eastchester /ID# 218445 — The Bronx

Texas

  • Mary Crowley Cancer Research /ID# 123760 — Dallas
  • University of Texas MD Anderson Cancer Center /ID# 154648 — Houston

Arizona

  • Scottsdale Healthcare /ID# 123761 — Scottsdale

Colorado

  • Univ of Colorado Cancer Center /ID# 123759 — Aurora

Trial Details

FieldValue
Enrollment Target 237 participants
Start Date 2014-01-15
Est. Completion 2026-08
Phase Phase 1

Sponsor

AbbVie

603 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02099058

The ClinicalTrials.gov registry entry for NCT02099058 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 237 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AbbVie, which has 603 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Advanced Solid Tumors Cancer appearing as the primary indexed condition, and to 4 interventions — of which Osimertinib is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02099058 reports 20 study locations spanning 12 distinct geographic areas — top geographies include California, Illinois, Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02099058 about?

NCT02099058 is a clinical study titled "A Study Evaluating the Safety, Pharmacokinetics (PK), and Preliminary Efficacy of ABBV-399 in Participants With Advanced Solid Tumors". This is a Phase 1/1b open-label study evaluating the safety, pharmacokinetics (PK), and preliminary efficacy of ABBV-399 as monotherapy and in combination with osimertinib, erlotinib, and nivolumab in participants with advanced solid tumors likely to express c-Met. Enrollment is closed for the monot...

What is the current status of trial NCT02099058?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 237 participants. The study started on 2014-01-15. Estimated completion is 2026-08.

What conditions does trial NCT02099058 study?

This clinical trial studies the following conditions: Advanced Solid Tumors Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02099058?

The interventions under investigation include: Osimertinib (DRUG), Nivolumab (DRUG), Erlotinib (DRUG), Telisotuzumab vedotin (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02099058?

This trial is sponsored by AbbVie, which has 603 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02099058 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, Illinois, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial