GANCICLOVIR SODIUM

Post-LOE

ganciclovir sodium

PharmaIN

ANDAINJECTIONINJECTABLE

Approved

Nov 2017

Lifecycle

Post-LOE

Competitive Pressure

30/100

Clinical Trials

Data completeness

4/8 — Partial

GANCICLOVIR SODIUM (ganciclovir sodium) by PharmaIN is [see microbiology ()] . Approved for cytomegalovirus (cmv) retinitis in immunocompromised adult patients, including patients with acquired immunodeficiency syndrome (aids) [see clinical studies ()], cmv disease in adult transplant recipients at risk for cmv disease [see clinical studies ()]. First approved in 2017.

Drug data last refreshed 18h ago

Mechanism of Action

[see Microbiology ()] .

Indications (1)

cytomegalovirus (CMV) retinitis in immunocompromised adult patients

Clinical Trials (1)

NCT00002034N/ACompleted

A Study of the Safety and Tolerance of Long-Term Therapy With Intravenous Cytovene (Ganciclovir Sodium) for Cytomegalovirus Retinitis in Persons With AIDS

100 enrolled

Cytomegalovirus RetinitisHIV Infections

Company

Worked on GANCICLOVIR SODIUM at PharmaIN? Share your interview experience or compensation data (+7 days Pro)

Data Sources

Drug label: DailyMed / FDA
Clinical trials: ClinicalTrials.gov
Patent data: FDA Orange Book
Spending data: CMS Medicare

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.