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poloxamer 188

Mast Therapeutics, Inc. · FDA-approved active Small molecule Quality 2/100

poloxamer 188 is a Small molecule drug developed by Mast Therapeutics, Inc.. It is currently FDA-approved.

Poloxamer 188, marketed by Mast Therapeutics, Inc., holds a unique position in its therapeutic segment with a key composition patent expiring in 2028. The drug's primary strength lies in its established market presence, leveraging its mechanism to address critical patient needs. The primary risk is the lack of revenue data and key trial results, which may limit investor confidence and competitive positioning.

At a glance

Generic namepoloxamer 188
SponsorMast Therapeutics, Inc.
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 poloxamer 188

What is poloxamer 188?

poloxamer 188 is a Small molecule drug developed by Mast Therapeutics, Inc..

Who makes poloxamer 188?

poloxamer 188 is developed and marketed by Mast Therapeutics, Inc. (see full Mast Therapeutics, Inc. pipeline at /company/mast-therapeutics-inc).

What development phase is poloxamer 188 in?

poloxamer 188 is FDA-approved (marketed).

Related

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