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HEXAMINOLEVULINATE

FDA-approved approved Small molecule Quality 20/100

HEXAMINOLEVULINATE is a drug. It is currently FDA-approved (first approved 2010).

Cysview is converted into PpIX and PAPs, which accumulate in neoplastic cells and fluoresce under specific light, aiding cystoscopic detection.

At a glance

Generic nameHEXAMINOLEVULINATE
ModalitySmall molecule
PhaseFDA-approved
First approval2010

Mechanism of action

Cysview, when instilled in the bladder, is taken up by mucosal cells and converted into PpIX and PAPs. These compounds accumulate more in cancerous cells than in normal cells, and when exposed to light, they emit a red fluorescence that helps identify tumors during cystoscopy.

Approved indications

No approved indications tracked.

Common side effects

Serious adverse events

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

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Frequently asked questions about HEXAMINOLEVULINATE

What is HEXAMINOLEVULINATE?

HEXAMINOLEVULINATE is a Small molecule drug.

How does HEXAMINOLEVULINATE work?

Cysview is converted into PpIX and PAPs, which accumulate in neoplastic cells and fluoresce under specific light, aiding cystoscopic detection.

When was HEXAMINOLEVULINATE approved?

HEXAMINOLEVULINATE was first approved on 2010.

What development phase is HEXAMINOLEVULINATE in?

HEXAMINOLEVULINATE is FDA-approved (marketed).

What are the side effects of HEXAMINOLEVULINATE?

Common side effects of HEXAMINOLEVULINATE include Bladder spasm, Dysuria, Hematuria, Bladder pain. Serious adverse events: Anaphylaxis, Anaphylactoid shock, Hypersensitivity reactions, Cystitis.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing