Last reviewed · How we verify

KIACTA (eprodisate disodium)

C.T. Development America, Inc. · Phase 3 active Small molecule

Eprodisate disodium inhibits glycosaminoglycan (GAG) synthesis and accumulation by blocking the formation of pathogenic protein-GAG complexes in amyloid-related diseases.

Eprodisate disodium inhibits glycosaminoglycan (GAG) synthesis and accumulation by blocking the formation of pathogenic protein-GAG complexes in amyloid-related diseases. Used for Transthyretin (TTR) amyloidosis.

At a glance

Generic nameKIACTA (eprodisate disodium)
SponsorC.T. Development America, Inc.
Drug classAmyloid inhibitor
TargetGlycosaminoglycan (GAG) synthesis and amyloid-GAG interaction
ModalitySmall molecule
Therapeutic areaRare Genetic Diseases / Amyloidosis
PhasePhase 3

Mechanism of action

Eprodisate is a small molecule that interferes with the interaction between amyloid proteins and glycosaminoglycans, which are thought to play a key role in amyloid fibril formation and tissue deposition. By reducing GAG-mediated amyloid stabilization and accumulation, the drug aims to slow or halt disease progression in amyloidosis. This mechanism targets the underlying pathophysiology of amyloid diseases rather than simply managing symptoms.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: