A Randomized Phase II Study of Tepotinib with or without Ramucirumab in Participants with MET Exon 14 Skipping Positive Stage IV or Recurrent Non-Small Cell Lung Cancer (Lung-MAP Sub-Study)
- Sponsor:
- SWOG
- Sponsor Study ID:
- S1900K
- CTO #:
- 104055
- NCT Number:
- NCT06031688
- Phase:
- II
- Protocol Type:
- Treatment
- Age Group:
- Adults
- Disease Sites:
- Lung
- Study Objectives:
- The primary objective is to compare the response rate (confirmed or unconfirmed, complete or partial) between participants with MET exon 14 skipping positive NSCLC randomized to tepotinib with or without ramucirumab. To compare the frequency of all-grade treatment- related peripheral edema as defined by CTCAE between the arms. To evaluate the frequency and severity of toxicities within each arm. To compare progression-free survival between the arms. To compare overall survival between the arms. To estimate the duration of response (DoR) among responders within each arm
- 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, Rangel, Christopher, at rangelc@musc.edu .
- Study Coordinator, Schumpp, Alec, at schumpp@musc.edu .
Trial opened at the following institutions:
Medical University of South Carolina