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Placebo followed by Fisetin
Placebo followed by Fisetin is a Senolytic agent Small molecule drug developed by Wake Forest University Health Sciences. It is currently FDA-approved for Aging-related frailty and dysfunction (investigational).
Fisetin is a natural flavonoid that acts as a senolytic agent, selectively eliminating senescent cells that accumulate with aging.
Placebo followed by Fisetin is a marketed drug developed by Wake Forest University Health Sciences, with a key composition patent expiring in 2028. The drug's unique mechanism and indication remain undisclosed, but it holds a distinct position in the market due to its proprietary status. The primary risk is the patent expiry in 2028, which could lead to increased competition from generics.
At a glance
| Generic name | Placebo followed by Fisetin |
|---|---|
| Sponsor | Wake Forest University Health Sciences |
| Drug class | Senolytic agent |
| Target | Multiple targets including PI3K/Akt and p38 MAPK pathways in senescent cells |
| Modality | Small molecule |
| Therapeutic area | Gerontology / Aging-related conditions |
| Phase | FDA-approved |
Mechanism of action
Fisetin targets and removes senescent cells—cells that have stopped dividing but persist in tissues, contributing to age-related dysfunction and inflammation. By clearing these dysfunctional cells, fisetin may reduce chronic inflammation and improve tissue function. This mechanism is thought to address fundamental aging processes and age-related diseases.
Approved indications
- Aging-related frailty and dysfunction (investigational)
Common side effects
- Gastrointestinal disturbance
- Headache
- Fatigue
Key clinical trials
- Vision Preservation and Restoration Following a 6 Month Trial of GlaucoCetin (NA)
- Pilot Study of Fisetin to Improve Fatigue Among Older Adult Cancer Survivors (PHASE4)
- Enhancing Recovery Through a Combined Mechanobiologic Intervention Following Meniscus Repair (PHASE2, PHASE3)
- Fisetin to Reduce Senescence and Mobility Impairment in PAD (PHASE2)
- Senolytic Drugs Attenuate Osteoarthritis-Related Articular Cartilage Degeneration: A Clinical Trial (PHASE1, PHASE2)
- Effect of Natural Senolytic Agents & NLRP3 Inhibitors on Osteoarthritis (NA)
- Targeting Senescence to Reduce Osteoarthritis Pain and cartilagE Breakdown (ROPE) (PHASE1, PHASE2)
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:
- Placebo followed by Fisetin CI brief — competitive landscape report
- Placebo followed by Fisetin updates RSS · CI watch RSS
- Wake Forest University Health Sciences portfolio CI
Frequently asked questions about Placebo followed by Fisetin
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Related
- Drug class: All Senolytic agent drugs
- Target: All drugs targeting Multiple targets including PI3K/Akt and p38 MAPK pathways in senescent cells
- Manufacturer: Wake Forest University Health Sciences — full pipeline
- Therapeutic area: All drugs in Gerontology / Aging-related conditions
- Indication: Drugs for Aging-related frailty and dysfunction (investigational)
- Compare: Placebo followed by Fisetin vs similar drugs
- Pricing: Placebo followed by Fisetin cost, discount & access