the placebo tablet and AP1189 tablet are identical.
Sponsors
Synact Pharma ApS
Conditions
Idiopathic membranous nephropathy and severe proteinuriaPolymyalgia rheumatica
Phase 2
An exploratory, randomized, double-blind, multicenter, placebo-controlled study to assess the safety, tolerability, pharmacokinetics, and efficacy of AP1189 daily doses versus placebo administered for 12 weeks as an add-on to patients, in ACE inhibitor or angiotensin II receptor blocker treatment, with idiopathic membranous nephropathy and severe proteinuria
RecruitingCTIS2024-518384-36-00
Start: 2020-08-31Target: 18Updated: 2024-10-28
A randomized, double blind, placebo-controlled, phase II, multicentre trial to explore the efficacy and safety of oral AP1189 tablets administered at the dose 100 mg/day for 12 weeks in patients diagnosed with polymyalgia rheumatica and in remission on glucocorticoid
Not yet recruitingCTIS2026-525343-33-00
Target: 60Updated: 2026-03-19