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NCT03539536 · ClinicalTrials.gov registry record · Phase 2
Study of Telisotuzumab Vedotin (ABBV-399) in Participants With Previously Treated c-Met+ Non-Small Cell Lung Cancer
A Phase 2 study of Non-Small Cell Lung Cancer, sponsored by AbbVie.
- Active
- Registry status
- Phase 2
- Development phase
- 270
- Enrollment target
- 20
- Study locations
NCT03539536: Active Phase 2 study of Non-Small Cell Lung Cancer, sponsored by AbbVie.
NCT03539536 is a Phase 2 study of Non-Small Cell Lung Cancer that is active but no longer recruiting, run by AbbVie. The registered enrollment target is 270 participants, below the 652-participant average among 454 other Non-Small Cell Lung Cancer trials with a reported enrollment target (59% lower). The trial reports 20 study locations across 9 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03539536, a Phase 2 study of Non-Small Cell Lung Cancer, is active but no longer recruiting, sponsored by AbbVie.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 2
- Development phase
- 270 participants
- Enrollment target
- 20
- Study locations
Study Summary
This study is designed to identify the target Non-Small Cell Lung Cancer (NSCLC) population(s) that overexpress c-Met (c-Met+) best suited for telisotuzumab vedotin therapy in the second line or third line setting (Stage 1) and then to expand the group(s) to further evaluate efficacy in the selected population(s) (Stage 2). After the Stage 2 global enrollment is completed, an additional cohort at an alternate dose level will evaluate the safety and efficacy of telisotuzumab vedotin (Stage 3).
Primary Outcome
ORR is defined as the percentage of participants with a confirmed complete response (CR) or confirmed partial response (PR) based on Response Evaluation Criteria in Solid Tumors (RECIST), version 1.1.
Conditions Studied
Interventions
- DRUG Telisotuzumab vedotin
Study Locations (20)
Illinois
- Northwestern University Feinberg School of Medicine /ID# 203239 - Chicago
- The University of Chicago Medical Center /ID# 203216 - Chicago
- Duplicate_NorthShore University HealthSystem /ID# 215583 - Evanston
- Ingalls Memorial Hosp /ID# 203228 - Harvey
- Joliet Oncology-Hematology Associates, LTD /ID# 203238 - Joliet
California
- University of California, Los Angeles /ID# 203219 - Los Angeles
- LA Hematology-Oncology Med Group /ID# 203338 - Orange
- Sutter Medical Center Sacramen /ID# 203299 - Sacramento
- Icri /Id# 227835 - Whittier
Florida
- Advanced Cancer Treatment Center /ID# 239565 - Brooksville
- AdventHealth Celebration /ID# 215649 - Celebration
- Duplicate_Mayo Clinic /ID# 218488 - Jacksonville
- Duplicate_AdventHealth Cancer Institute - Orlando /ID# 239960 - Orlando
Colorado
- Univ of Colorado Cancer Center /ID# 203212 - Aurora
- Duplicate_Rocky Mountain Cancer Centers - Lone Tree /ID# 215789 - Lone Tree
Alabama
- University of South Alabama /ID# 212939 - Mobile
Arizona
- Mayo Clinic Arizona /ID# 218550 - Phoenix
Arkansas
- Highlands Oncology Group, PA /ID# 215600 - Springdale
Hawaii
- Straub Clinic and Hospital /ID# 217905 - Honolulu
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 270 participants |
| Start Date | 2018-10-10 |
| Est. Completion | 2026-08 |
| Phase | Phase 2 |
What the registry record for NCT03539536 still lists
NCT03539536 is an interventional study that assigns participants to a tested intervention. The registered 270 participants enrollment target is mid-sized for trials with a published cap, below the 652-participant average among 454 other Non-Small Cell Lung Cancer trials with a reported enrollment target (59% lower).
The record links to 1 condition, with Non-Small Cell Lung Cancer appearing as the primary indexed condition, and to 1 intervention - of which Telisotuzumab vedotin is the first listed.
NCT03539536 names 20 study sites across 9 states, led by Illinois, California, Florida.
Frequently Asked Questions
What is clinical trial NCT03539536 about?
NCT03539536 is a clinical study titled "Study of Telisotuzumab Vedotin (ABBV-399) in Participants With Previously Treated c-Met+ Non-Small Cell Lung Cancer". This study is designed to identify the target Non-Small Cell Lung Cancer (NSCLC) population(s) that overexpress c-Met (c-Met+) best suited for telisotuzumab vedotin therapy in the second line or third line setting (Stage 1) and then to expand the group(s) to further evaluate efficacy in the selected...
What is the current status of trial NCT03539536?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 270 participants. The study started on 2018-10-10. Estimated completion is 2026-08.
What conditions does trial NCT03539536 study?
This clinical trial studies the following conditions: Non-Small Cell Lung Cancer.
What interventions are being tested in trial NCT03539536?
The interventions under investigation include: Telisotuzumab vedotin (DRUG).
Who is sponsoring clinical trial NCT03539536?
This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03539536 being conducted?
This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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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 NCT03539536's enrollment target sits among peer trials
270 139th of 454 higher than 315 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.
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