A Randomized Phase II Study of Amivantamab (JNJ-61186372) and Hyaluronidase (rHuPH20) Versus Cetuximab in Immunocompromised Participants with Recurrent Inoperable or Metastatic Cutaneous Squamous Cell Carcinoma
- Sponsor:
- SWOG
- Sponsor Study ID:
- SN2426
- CTO #:
- 104387
- NCT Number:
- NCT07042295
- Phase:
- II
- Protocol Type:
- Treatment
- Age Group:
- Adults
- Disease Sites:
- Other Skin
- Study Objectives:
- Safety run-in (Cohort A): To evaluate the safety and preliminary efficacy of amivantamab monotherapy in patients with locoregionally incurable or metastatic cutaneous squamous cell carcinoma and an active immunosuppressed condition. Randomized comparison (Cohort B): To compare progression-free survival (PFS) of amivantamab monotherapy versus cetuximab monotherapy in patients with locoregionally incurable or metastatic cutaneous squamous cell carcinoma and an active immunosuppressed condition.
- eConsent:
- Not available
- Study Documents:
-
Open Study Documents
(MUSC NetID required for document access)
For more information about this trial please contact the study team:
-
Medical University of South Carolina
- Principal Investigator, Kaczmar, John, at kaczmar@musc.edu
- Study Coordinator, Langley, Madelyn, at langlema@musc.edu
Trial opened at the following institutions:
Medical University of South Carolina