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Lipaglyn (SAROGLITAZAR)

Cadila Healthcare · FDA-approved active Small molecule ✓ Verified May 2026 Quality 30/100

Lipaglyn (generic name: SAROGLITAZAR) is a Small molecule drug developed by Cadila Healthcare. It is currently FDA-approved for Diabetic dyslipidemia associated with type 2 diabetes mellitus.

Lipaglyn is a small molecule that acts as an agonist to the peroxisome proliferator-activated receptor alpha. It is classified as a peroxisome proliferator-activated receptor alpha agonist.

At a glance

Generic nameSAROGLITAZAR
SponsorCadila Healthcare
TargetPeroxisome proliferator-activated receptor alpha
ModalitySmall molecule
Therapeutic areaMetabolic
PhaseFDA-approved

Approved indications

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

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Frequently asked questions about Lipaglyn

What is Lipaglyn?

Lipaglyn (SAROGLITAZAR) is a Small molecule drug developed by Cadila Healthcare, indicated for Diabetic dyslipidemia associated with type 2 diabetes mellitus.

What is Lipaglyn used for?

Lipaglyn is indicated for Diabetic dyslipidemia associated with type 2 diabetes mellitus.

Who makes Lipaglyn?

Lipaglyn is developed and marketed by Cadila Healthcare (see full Cadila Healthcare pipeline at /company/cadila-healthcare).

What is the generic name of Lipaglyn?

SAROGLITAZAR is the generic (nonproprietary) name of Lipaglyn.

What development phase is Lipaglyn in?

Lipaglyn is FDA-approved (marketed).

What does Lipaglyn target?

Lipaglyn targets Peroxisome proliferator-activated receptor alpha.

Related

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