PRTX-100-202 Open-Label, Dose Escalation Study in Adult Patients With ITP

Status Terminated

Clinical Trial Summary

Pre-clinical and clinical evaluations show that PRTX- 100 has biological activity that may lead to improved platelet levels where these are decreased due to immunological pathologies and that PRTX-100 has an acceptable safety profile. In vivo treatment with PRTX-100 has been shown to raise platelet counts in a mouse model of immune thrombocytopenia (ITP). The primary objective of the study is to assess the efficacy of PRTX-100 in terms of platelet response in patients with chronic/persistent ITP.

Funding Source - FDA OOPD (1R01FD005750-01A1)

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Immune Thrombocytopenia
Purpura, Thrombocytopenic, Idiopathic
Thrombocytopenia

Clinical Trial Details

NCT number	NCT02401061
Study type	Interventional
Source	Protalex, Inc.
Contact
Status	Terminated
Phase	Phase 1/Phase 2
Start date	September 2015
Completion date	June 4, 2019

View Details

See also
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