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Active, not recruiting Phase 2 Interventional

Enhanced Dermatological Care to Reduce Rash and Paronychia in Epidermal Growth Factor Receptor (EGRF)-Mutated Non-Small Cell Lung Cancer (NSCLC) Treated First-line With Amivantamab Plus Lazertinib

ClinicalTrials.gov ID: NCT06120140

Public ClinicalTrials.gov record NCT06120140. 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 22, 2026, 10:20 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 2, Open-Label, Randomized Trial Evaluating the Impact of Enhanced Versus Standard Dermatologic Management on Selected Dermatologic Adverse Events Among Patients With Locally Advanced or Metastatic EGFR-Mutated NSCLC Treated First-Line With Amivantamab + Lazertinib

Brief summary

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

The purpose of this study is to evaluate whether enhanced dermatologic management can reduce incidence of grade greater than or equal to (\>=) 2 dermatologic adverse events of interest (DAEIs) when compared with standard-of-care skin management and with modified enhanced dermatologic management in participants with locally advanced or metastatic stage IIIB/C-IV epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC) treated first-line with amivantamab and lazertinib. The study also includes Expansion cohorts (in 2 different schedules) to evaluate enhanced dermatologic management and early intervention for DAEIs or paronychia, in participants receiving subcutaneous amivantamab and lazertinib. A substudy will enroll participants from Arms A and B who experience specific new-onset or persistent DAEIs (Grade \>=2) during treatment with intravenous (IV) amivantamab and lazertinib. This substudy aims to assess the reactive use of dermatologic treatment strategies in these participants.

Study identification

NCT ID
NCT06120140
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
305 participants

Conditions and interventions

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
Feb 16, 2024 (Actual)
Primary completion
May 31, 2027 (Estimated)
Completion
Jun 30, 2030 (Estimated)
Last update posted
Sep 25, 2026

2024 – 2030

United States locations

U.S. sites
28
U.S. states
13
U.S. cities
28
Facility City State ZIP Site status
Ironwood Cancer and Research Center Chandler Arizona 85224 —
City of Hope Duarte California 91010 —
Providence Fullerton Fullerton California 92835 —
Los Angeles Cancer Network Glendale California 91204 —
City of Hope Seacliff Huntington Beach California 92648 —
City of Hope Orange County Lennar Foundation Cancer Center Irvine California 92618 —
City of Hope Long Beach Elm Long Beach California 90813 —
Cancer and Blood Specialty Clinic Los Alamitos California 90720 —
Keck Hospital of USC Los Angeles California 90033 —
USC Norris Oncology Hematology Newport Beach Newport Beach California 92663 —
Kaiser Permanente Oakland Medical Center Oakland California 94611 —
Kaiser Permanente Roseville Medical Center Roseville California 95661 —
Kaiser Permanente San Francisco Medical Center San Francisco California 94115 —
Kaiser Permanente Santa Clara Medical Center Santa Clara California 95051 —
City of Hope South Pasadena South Pasadena California 91030 —
Kaiser Permanente Northern California Vallejo California 94589 —
Kaiser Permanente Walnut Creek Medical Center Walnut Creek California 94596 —
University Cancer & Blood Center Athens Georgia 30607 —
Hope and Healing Care Hinsdale Illinois 60521 —
Oncology Hematology Associates Springfield Missouri 65807 —
Renown Health Medical Oncology Reno Nevada 89502 —
Hunterdon Hematology Oncology Flemington New Jersey 08822 —
Clinical Research Alliance Inc Westbury New York 11590 —
Regional Medical Oncology Center Wilson North Carolina 27893 —
University Hospitals Cleveland Medical Center Cleveland Ohio 44106 —
Virginia Cancer Specialists Fairfax Virginia 22031 —
Valley Medical Center Renton Washington 98055 —
Gundersen Health System West Salem Wisconsin 54669 —

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 65 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06120140, 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 Sep 25, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06120140 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →