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Dutasteride plus tamsulosin

GlaxoSmithKline · FDA-approved active Small molecule Quality 5/100

Dutasteride plus tamsulosin is a Small molecule drug developed by GlaxoSmithKline. It is currently FDA-approved.

Dutasteride plus tamsulosin, marketed by GlaxoSmithKline, is a combination therapy currently available in the market. The key composition patent is set to expire in 2028, providing a period of exclusivity that supports its market position. The primary risk is the potential increase in competition following the patent expiry in 2028.

At a glance

Generic nameDutasteride plus tamsulosin
SponsorGlaxoSmithKline
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

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about Dutasteride plus tamsulosin

What is Dutasteride plus tamsulosin?

Dutasteride plus tamsulosin is a Small molecule drug developed by GlaxoSmithKline.

Who makes Dutasteride plus tamsulosin?

Dutasteride plus tamsulosin is developed and marketed by GlaxoSmithKline (see full GlaxoSmithKline pipeline at /company/gsk).

What development phase is Dutasteride plus tamsulosin in?

Dutasteride plus tamsulosin is FDA-approved (marketed).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing