Last reviewed · How we verify

SUCROSE

FDA-approved active Small molecule Quality 15/100

Sucrose is a marketed drug primarily indicated for Iron Deficiency Anemia in CKD patients on hemodialysis, with a key composition patent expiring in 2028. Its primary strength lies in its established market presence and indication for a specific patient population. The primary risk is the potential increase in competition as the key patent approaches expiration in 2028.

At a glance

Generic nameSUCROSE
Drug classParenteral Iron Replacement [EPC]
ModalitySmall molecule
PhaseFDA-approved

Approved indications

Common side effects

Serious adverse events

Drug interactions

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: