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SUGEMALIMAB

FDA-approved approved Monoclonal antibody Quality 6/100

Sugemalimab is a marketed drug that modulates the immune response by binding to a specific target on cells. The key composition patent for sugemalimab is set to expire in 2028, providing a clear timeline for potential generic competition. Without specific revenue or trial results, the primary risk remains the competitive landscape, which could impact market share and profitability post-patent expiry.

At a glance

Generic nameSUGEMALIMAB
ModalityMonoclonal antibody
Therapeutic areaImmunology
PhaseFDA-approved
First approval2024

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

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
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
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: