Drugs / eprodisate

Trials 2

20022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 2/31 trial · 1 met primary
Phase 2/3 NCT00035334 Oct 2001 → Dec 2004 AA amyloidosis, digestive system disorder, familial Mediterranean fever, nephrotic syndrome +1 Bellus Health Inc. - a GSK company Completed Met primary
Phase 31 trial
Phase 3 NCT01215747 Nov 2010 → Jan 2016 amyloidosis C.T. Development America, Inc. Completed No outcome recorded
Comparator or background therapy1 trial
Phase 2 NCT00675857 Comparator Apr 2008 → Jan 2010 metabolic syndrome X, type 2 diabetes mellitus Bellus Health Inc. - a GSK company Completed No outcome recorded

Evidence & citations 10 cited values

Every value below carries the sentence it was read from. 4 sources stand behind the page.

FieldValueCited text
Known as eprodisate ClinicalTrials.gov intervention name — accepted as the source's own label NCT01215747 ↗
Known as Disodium eprodisate ChEMBL registry synonym — accepted as the source's own label CHEMBL2111092 ↗
Known as eprodisate disodium “KIACTA (eprodisate disodium)” NCT01215747 ↗
1

“NC-503 (eprodisate disodium)” NCT00675857 ↗

Known as Eprodisato ChEMBL registry synonym — accepted as the source's own label CHEMBL2111092 ↗
Known as KIACTA “KIACTA (eprodisate disodium)” NCT01215747 ↗
Known as NC-503 ClinicalTrials.gov intervention name — accepted as the source's own label NCT00035334 ↗
1

NCT00675857 ↗

Known as NSC-240395 ChEMBL registry synonym — accepted as the source's own label CHEMBL2111092 ↗
Known as NSC-760403 ChEMBL registry synonym — accepted as the source's own label CHEMBL2111092 ↗
Modality Small molecule — CHEMBL2111092 ↗
Route Oral “Orally 1 to 3 capsules (Kiacta 400 mg) twice daily and adjusted as per the Creatine Clearance (CrCl) level increases or decreases.” NCT01215747 ↗