A Phase 1 Study of SEA-CD70 in Myeloid Malignancies
- Sponsor:
- Seattle Genetics, Inc.
- Sponsor Study ID:
- SEA-CD70
- CTO #:
- 103164
- NCT Number:
- NCT04227847
- Phase:
- I
- Protocol Type:
- Treatment
- Age Group:
- Adults
- Disease Sites:
- Myeloid and Monocytic Leukemia
- Study Objectives:
- This is a phase 1, open-label, multicenter, dose-escalation, and cohort expansion study designed to evaluate the safety, tolerability, PK, and antitumor activity of SEA-CD70 in adults with myeloid malignancies. The study will be conducted in up to 3 parts. Part A is a dose escalation cohort designed to identify the MTD or recommended expansion dose of SEA-CD70 in subjects with relapsed/refractory (HMA-failure) MDS. Part B is an expansion cohort designed to evaluate the safety and tolerability of SEA-CD70 in subjects with relapsed/refractory (HMA-failure) MDS. Part C is an expansion cohort designed to evaluate the safety and tolerability of SEA-CD70 in subjects with relapsed/refractory AML.
- 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, Baratam, Praneeth, at baratamp@musc.edu .
- Study Coordinator, Baker, Hana, at bakerhan@musc.edu .
Trial opened at the following institutions:
Medical University of South Carolina