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Clinical Trial Summary

To characterise the safety and tolerability of NG-641 in patients with metastatic or advanced epithelial tumours.


Clinical Trial Description

To characterise the safety and tolerability of NG-641 in patients with metastatic or advanced epithelial tumours. The Phase 1a part of the study is a dose-escalation and dose-optimization phase investigating NG-641 administration by intravenous (IV) infusion in a range of tumour types. The Phase 1b part of the study will investigate the selected optimized multicycle dosing regimen as a monotherapy in up to three cohorts of patients with specific tumour types (Dose Expansion Cohorts A, B and C). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04053283
Study type Interventional
Source Akamis Bio
Contact Akamis Bio
Phone +44 1235835328
Email enquiries@akamisbio.com
Status Recruiting
Phase Phase 1
Start date January 23, 2020
Completion date December 31, 2023

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