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Clinical Trial Summary

This is an open-label, non-randomized study to evaluate the PD, PK, and safety of 500 to 2000 mg/m2 PTX-100 in patients with advanced malignancies. PTX-100 will be administered by IV infusion over 60 minutes on days 1 to 5 of a 14-day cycle for 4 cycles unless toxicity is observed. Dose escalation is complete and the expansion is open and actively recruiting PTCL patients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03900442
Study type Interventional
Source Prescient Therapeutics, Ltd.
Contact Leanne West
Email lwest@ptxtherapeutics.com
Status Recruiting
Phase Phase 1
Start date September 1, 2019
Completion date April 30, 2023

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