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
Summary
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.
Timeline
- Start
- 2024-02-16
- Primary completion
- 2027-05-31
- Completion
- 2030-06-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Chlorhexidine | Small molecule | — | Topical |
| Subject | Clindamycin | Unknown | — | Topical |
| Subject | Clobetasol | Small molecule | — | Topical |
| Subject | Doxycycline | Small molecule | 100 mg | Oral |
| Subject | Minocycline | Small molecule | 100 mg | Oral |
| Subject | Propranolol | Small molecule | — | — |
| Subject | Timolol | Other / unclassified | — | Topical |
| Subject | Zinc gluconate | Small molecule | — | — |
| Background | Amivantamab | Monoclonal antibody | — | Intravenous |
| Background | Lazertinib | Small molecule | — | Oral |