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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 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 658-participant average among 449 other Non-Small Cell Lung Cancer trials with a reported enrollment target (35% lower). The trial reports 20 study locations across 18 states.
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.
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
| Field | Value |
|---|---|
| Enrollment Target | 430 participants |
| Start Date | 2025-12-10 |
| Est. Completion | 2030-09 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07155187
The ClinicalTrials.gov registry entry for NCT07155187 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 430 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 658-participant average among 449 other Non-Small Cell Lung Cancer trials with a reported enrollment target (35% lower). The listed sponsor is AbbVie, which has 526 total studies on file at ClinicalTrials.gov.
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 reports 20 study locations spanning 18 distinct geographic areas - top geographies include 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.
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Related
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