TerminatedPhase 1NCT04348916
Study of ONCR-177 Alone and in Combination With PD-1 Blockade in Adult Subjects With Advanced and/or Refractory Cutaneous, Subcutaneous or Metastatic Nodal Solid Tumors or With Liver Metastases of Solid Tumors
Studying Cutaneous neuroendocrine carcinoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Oncorus, Inc.
- Principal Investigator
- John Goldberg, MDOncorus, Inc.
- Intervention
- ONCR-177(biological)
- Enrollment
- 66 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2020 – 2023
Study locations (11)
- City of Hope, Duarte, California, United States
- Sarah Cannon Research Institute at HealthONE, Denver, Colorado, United States
- Moffitt Cancer Center, Tampa, Florida, United States
- Emory University, Atlanta, Georgia, United States
- Massachusetts General Hospital, Boston, Massachusetts, United States
- Dana-Farber Cancer Institute, Boston, Massachusetts, United States
- Roswell Park Cancer Institute, Buffalo, New York, United States
- The Ohio State University Wexner Medical Center James Cancer Hospital, Columbus, Ohio, United States
- Sarah Cannon Research Institute - Tennessee Oncology, Nashville, Tennessee, United States
- The University of Texas at Austin, Austin, Texas, United States
- University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada
Collaborators
Merck Sharp & Dohme LLC
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT04348916 on ClinicalTrials.govOther trials for Cutaneous neuroendocrine carcinoma
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