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Sandimmun Neoral®, CellCept® and prednisolone

University of Oslo School of Pharmacy · FDA-approved active Small molecule Quality 5/100

Sandimmun Neoral®, CellCept® and prednisolone is a Small molecule drug developed by University of Oslo School of Pharmacy. It is currently FDA-approved.

Sandimmun Neoral®, CellCept®, and prednisolone are marketed immunosuppressive drugs developed by the University of Oslo School of Pharmacy, with a key composition patent expiring in 2028. The combination of these drugs offers a robust immunosuppressive effect, which is a significant competitive advantage in preventing organ rejection post-transplant. The primary risk is the patent expiry in 2028, which could lead to increased competition from generic alternatives.

At a glance

Generic nameSandimmun Neoral®, CellCept® and prednisolone
SponsorUniversity of Oslo School of Pharmacy
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

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Frequently asked questions about Sandimmun Neoral®, CellCept® and prednisolone

What is Sandimmun Neoral®, CellCept® and prednisolone?

Sandimmun Neoral®, CellCept® and prednisolone is a Small molecule drug developed by University of Oslo School of Pharmacy.

Who makes Sandimmun Neoral®, CellCept® and prednisolone?

Sandimmun Neoral®, CellCept® and prednisolone is developed and marketed by University of Oslo School of Pharmacy (see full University of Oslo School of Pharmacy pipeline at /company/university-of-oslo-school-of-pharmacy).

What development phase is Sandimmun Neoral®, CellCept® and prednisolone in?

Sandimmun Neoral®, CellCept® and prednisolone is FDA-approved (marketed).

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