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Clinical Trial Summary

This is a Phase II, open-label study designed to To evaluate the safety and efficacy of NM8074 in reducing proteinuria relative to baseline in IgAN patients after 99 days of treatment.


Clinical Trial Description

The proposed study, NM8074-IgAN-601, will enroll a planned total of 10 patients as subjects for the trial. All subjects will be administered 17 mg/kg of NM8074 intravenously every week, for a total of 15 doses from Day 1 to Day 99 of the Treatment Period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06454110
Study type Interventional
Source NovelMed Therapeutics
Contact Rekha Bansal, PhD
Phone 2164402696
Email clinicalsae@novelmed.com
Status Not yet recruiting
Phase Phase 2
Start date November 2025
Completion date July 2027

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