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Phase I Study of NEO-201 in Adults With Chemo-Resistant Solid Tumors, Including Pancreatic Cancer

Summary

The purpose of this phase I study is to determine the safety including dose limiting toxicity (DLT) and maximal tolerated dose of the monoclonal antibody NEO-201 in patients with solid tumors (cancer) which has not responded to standard treatments.

General Information

NCT#: NCT03476681
Study ID: PB-1801
Trial Phase: Phase I

Trial Sponsor: Precision Biologics
Therapies Used in This Trial: NEO-201

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Site Information

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