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Remifentanyl

Kocaeli University · FDA-approved active Small molecule Quality 30/100

Remifentanyl, marketed by Kocaeli University, is positioned in the acute postoperative pain segment. The drug's key strength lies in its mechanism of action, which is currently unspecified but likely contributes to its efficacy in managing postoperative pain. The primary risk is the key composition patent expiry in 2028, which could lead to increased competition from generics.

At a glance

Generic nameRemifentanyl
Also known asultiva, Ultiva
SponsorKocaeli University
TargetMu-type opioid receptor, Mu-type opioid receptor
ModalitySmall molecule
Therapeutic areaPain
PhaseFDA-approved

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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