
Pipeline Database
UB511
Pramipexole Dihydrochloride Sustained-Release Tablet
UB511
ProductPramipexole Dihydrochloride Sustained-Release Tablet
Strength0.375, 0.75mg
IndicationsParkinson's disease
TherapeuticsNeurology
GMPUS - FDA
RegistrationUnited States; China
ModalitiesSmall Molecule
Exclusive Summary
- - About 8.5 million people live with Parkinson’s globally and aging will keep demand rising; ER pramipexole has a stable and expanding prescription base.
- - Key ER formulation patents/exclusivities have largely expired, with broad generic entry since 2017–2021 across major markets.
- - US registration and FDA-cGMP manufacturing enable reliance/abridged approvals and efficient multi-region distribution.
- - Once-daily SR smooths plasma levels and improves adherence, suitable as early monotherapy (selected patients) and as add-on to levodopa.
- - Pricing 70–90% below brand supports competitiveness in both tenders and retail channels.
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