AP1189 Tablet
Sponsors
Synact Pharma ApS
Conditions
Idiopathic membranous nephropathy and severe proteinuriaPolymyalgia rheumaticaRheumatoid Arthritis
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, dose response, phase II, multicentre trial to evaluate the efficacy and safety of oral AP1189 administered at the doses of 40, 70, or 100 mg for 12 weeks in combination with methotrexate, in DMARD-naïve participants with early rheumatoid arthritis and active inflammation.
RecruitingCTIS2024-514981-37-00
Start: 2024-12-05Target: 172Updated: 2025-12-12
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