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Fentanyl TAIFUN
Fentanyl TAIFUN is a transdermal or inhalation formulation of fentanyl, a potent synthetic opioid agonist that binds to mu-opioid receptors in the central nervous system to produce analgesia and sedation.
Fentanyl TAIFUN is a transdermal or inhalation formulation of fentanyl, a potent synthetic opioid agonist that binds to mu-opioid receptors in the central nervous system to produce analgesia and sedation. Used for Moderate to severe pain (specific indication pending phase 3 results).
At a glance
| Generic name | Fentanyl TAIFUN |
|---|---|
| Sponsor | Akela Pharma, Inc. |
| Drug class | Opioid analgesic (synthetic opioid) |
| Target | Mu-opioid receptor (OPRM1) |
| Modality | Small molecule |
| Therapeutic area | Pain Management |
| Phase | Phase 3 |
Mechanism of action
Fentanyl acts as a mu-opioid receptor agonist, activating inhibitory pathways in the spinal cord and brain that reduce pain signal transmission and perception. The TAIFUN formulation appears to be a delivery system variant designed to optimize pharmacokinetics and patient tolerability. By modulating opioid receptor signaling, fentanyl produces dose-dependent analgesia, sedation, and respiratory depression.
Approved indications
- Moderate to severe pain (specific indication pending phase 3 results)
Common side effects
- Respiratory depression
- Constipation
- Nausea
- Dizziness
- Sedation
- Pruritus
Key clinical trials
- Safety of Fentanyl TAIFUN Treatment (PHASE3)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial 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:
- Fentanyl TAIFUN CI brief — competitive landscape report
- Fentanyl TAIFUN updates RSS · CI watch RSS
- Akela Pharma, Inc. portfolio CI