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Sodium Polystyrene Sulfonate Oral Suspension [SPS]
Sodium Polystyrene Sulfonate Oral Suspension [SPS] is a Small molecule drug developed by University of California, Irvine. It is currently FDA-approved. Also known as: Kayexalate.
Sodium Polystyrene Sulfonate Oral Suspension (SPS) is a marketed drug developed by the University of California, Irvine, with a key composition patent expiring in 2028. The drug's primary strength lies in its established market presence and the protection offered by its patent until 2028. The primary risk is the potential increase in competition following the patent expiry in 2028.
At a glance
| Generic name | Sodium Polystyrene Sulfonate Oral Suspension [SPS] |
|---|---|
| Also known as | Kayexalate |
| Sponsor | University of California, Irvine |
| Modality | Small molecule |
| Phase | FDA-approved |
Approved indications
Common side effects
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Sodium Polystyrene Sulfonate Oral Suspension [SPS] CI brief — competitive landscape report
- Sodium Polystyrene Sulfonate Oral Suspension [SPS] updates RSS · CI watch RSS
- University of California, Irvine portfolio CI
Frequently asked questions about Sodium Polystyrene Sulfonate Oral Suspension [SPS]
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Is Sodium Polystyrene Sulfonate Oral Suspension [SPS] also known as anything else?
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Related
- Manufacturer: University of California, Irvine — full pipeline
- Also known as: Kayexalate
- Compare: Sodium Polystyrene Sulfonate Oral Suspension [SPS] vs similar drugs
- Pricing: Sodium Polystyrene Sulfonate Oral Suspension [SPS] cost, discount & access