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Clinical Trial Summary

This is an extension study, to provide continued access to PRO 140 to subjects who complete participation in PRO140_CD02 and continue to receive clinical benefit and would require PRO 140 to form a viable regimen, in the opinion of the treating physician. The patient population for this trial are treatment-experienced HIV infected patients with CCR5-tropic virus who demonstrate evidence of HIV-1 suppression after successfully completed 24 weeks of treatment in the PRO140_CD02 study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02990858
Study type Interventional
Source CytoDyn, Inc.
Contact
Status Active, not recruiting
Phase Phase 2/Phase 3
Start date November 3, 2016
Completion date August 2022

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