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NCT07155187 · ClinicalTrials.gov registry record · Phase 2

A Study to Assess Adverse Events and Change in Disease Activity of Intravenous (IV) Telisotuzumab Adizutecan Compared to Standard of Care in Adult Participants With Locally Advanced or Metastatic EGFR-Mutated Non-Squamous Non-Small Cell Lung Cancer

A Phase 2 study of Non-Small Cell Lung Cancer, sponsored by AbbVie.

Recruiting
Registry status
Phase 2
Development phase
430
Enrollment target
20
Study locations

NCT07155187: Recruiting Phase 2 study of Non-Small Cell Lung Cancer, sponsored by AbbVie.

NCT07155187 is a Phase 2 study of Non-Small Cell Lung Cancer that is actively recruiting participants, run by AbbVie. The registered enrollment target is 430 participants, below the 651-participant average among 454 other Non-Small Cell Lung Cancer trials with a reported enrollment target (34% lower). The trial reports 20 study locations across 18 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07155187, a Phase 2 study of Non-Small Cell Lung Cancer, is actively recruiting participants, sponsored by AbbVie.

RECRUITING
Registry status
Phase 2
Development phase
430 participants
Enrollment target
20
Study locations

Study Summary

Non-small cell lung cancer (NSCLC) is a common type of lung cancer where abnormal cells in the lungs grow out of control. The purpose of this study is to assess adverse events and change in disease activity of telisotuzumab adizutecan compared to standard of care (SOC). Telisotuzumab adizutecan is an investigational drug being developed for the treatment of NSCLC. This study will be divided into two stages, in the first stage (phase 2) participants will receive 1 of 2 doses of telisotuzumab adizutecan. In the second stage (phase 3) participants will receive the recommended phase 3 dose (RP3D) of telisotuzumab adizutecan, from the previous stage, or SOC. Approximately 430 adult participants with NSCLC will be enrolled in the study in 200 sites around the world. In phase 2, participants will receive 1 of 2 intravenous (IV) doses of telisotuzumab adizutecan. In phase 3, participants will receive the IV RP3D of telisotuzumab adizutecan, or SOC. The study will run for a duration of approximately 69 months. 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.

Primary Outcome

OR is defined as participants achieving a best overall response of confirmed complete response (CR) or confirmed partial response (PR) per the BICR based on Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.

Conditions Studied

Interventions

  • DRUG Telisotuzumab Adizutecan
  • DRUG Standard of Care

Study Locations (20)

Tennessee

  • Tennessee Cancer Specialists - Knoxville - Old Weisgarber Road /ID# 277891 - Knoxville
  • SCRI Oncology Partners /ID# 276959 - Nashville

Victoria

  • St Vincent's Hospital Melbourne /ID# 277002 - Fitzroy
  • Sunshine Hospital /ID# 276894 - St Albans

Arkansas

  • Highlands Oncology Group - Springdale /ID# 277132 - Springdale

Florida

  • Cancer Care Centers of Brevard- Rockledge /ID# 277853 - Rockledge

Minnesota

  • HealthPartners Cancer Research Center /ID# 277339 - Saint Louis Park

Nebraska

  • Nho - Revive Research Institute /ID# 277569 - Lincoln

New Jersey

  • Astera Cancer Care /ID# 277570 - East Brunswick

Washington

  • Northwest Cancer Specialists - Vancouver /ID# 277855 - Vancouver

Trial Details

FieldValue
Enrollment Target 430 participants
Start Date 2025-12-10
Est. Completion 2030-09
Phase Phase 2
AbbVie

526 total trials

What NCT07155187 shows while recruiting

NCT07155187 is an interventional study that assigns participants to a tested intervention. The registered 430 participants enrollment target is mid-sized for trials with a published cap, below the 651-participant average among 454 other Non-Small Cell Lung Cancer trials with a reported enrollment target (34% lower).

The record links to 1 condition, with Non-Small Cell Lung Cancer appearing as the primary indexed condition, and to 2 interventions - of which Telisotuzumab Adizutecan is the first listed.

NCT07155187 names 20 study sites across 18 states, led by Tennessee, Victoria, Arkansas.

Frequently Asked Questions

What is clinical trial NCT07155187 about?

NCT07155187 is a clinical study titled "A Study to Assess Adverse Events and Change in Disease Activity of Intravenous (IV) Telisotuzumab Adizutecan Compared to Standard of Care in Adult Participants With Locally Advanced or Metastatic EGFR-Mutated Non-Squamous Non-Small Cell Lung Cancer". Non-small cell lung cancer (NSCLC) is a common type of lung cancer where abnormal cells in the lungs grow out of control. The purpose of this study is to assess adverse events and change in disease activity of telisotuzumab adizutecan compared to standard of care (SOC). Telisotuzumab adizutecan is ...

What is the current status of trial NCT07155187?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 430 participants. The study started on 2025-12-10. Estimated completion is 2030-09.

What conditions does trial NCT07155187 study?

This clinical trial studies the following conditions: Non-Small Cell Lung Cancer.

What interventions are being tested in trial NCT07155187?

The interventions under investigation include: Telisotuzumab Adizutecan (DRUG), Standard of Care (DRUG).

Who is sponsoring clinical trial NCT07155187?

This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07155187 being conducted?

This trial has 20 study locations across Arkansas, Florida, Minnesota, Nebraska, New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Non-Small Cell Lung Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07155187's enrollment target sits among peer trials

430 91st of 454 higher than 364 of 454 other Non-Small Cell Lung Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Non-Small Cell Lung Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07155187, the US trial registry maintained by the National Library of Medicine. NCT07155187 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.