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Clinical Trial Summary

This is a phase 1 dose escalation study to characterize the feasibility, safety and tolerability of MCY-M11 when administered as an intraperitoneal (IP) infusion for 3 weekly doses for women with platinum resistant high grade serous adenocarcinoma of the ovary, primary peritoneum, or fallopian tube, and subjects with peritoneal mesothelioma with recurrence after prior chemotherapy. The study will also assess multiple cycles of treatment and adding preconditioning with cyclophosphamide.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03608618
Study type Interventional
Source MaxCyte, Inc.
Contact
Status Terminated
Phase Phase 1
Start date August 27, 2018
Completion date August 24, 2021

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