Last reviewed · How we verify

Intermitent dosing as per SMPC

Ivan Šitum, MD · FDA-approved active Small molecule ✓ Verified May 2026 Quality 2/100

Intermitent dosing as per SMPC is a Small molecule drug developed by Ivan Šitum, MD. It is currently FDA-approved.

Intermittent dosing of ceftazidime/avibactam, as per the Summary of Product Characteristics (SMPC), is used to treat severe infections. This dosing modality is a small molecule intervention, classified as such in the ChEMBL database, and has been studied in clinical trials, including NCT06811727, which compared it to continuous infusion in critically ill patients.

At a glance

Generic nameIntermitent dosing as per SMPC
SponsorIvan Šitum, MD
ModalitySmall molecule
PhaseFDA-approved

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
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:

Frequently asked questions about Intermitent dosing as per SMPC

What is Intermitent dosing as per SMPC?

Intermitent dosing as per SMPC is a Small molecule drug developed by Ivan Šitum, MD.

Who makes Intermitent dosing as per SMPC?

Intermitent dosing as per SMPC is developed and marketed by Ivan Šitum, MD (see full Ivan Šitum, MD pipeline at /company/ivan-itum-md).

What development phase is Intermitent dosing as per SMPC in?

Intermitent dosing as per SMPC is FDA-approved (marketed).

Related

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