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IndexedBuilt automatically from public databases on 2026-09-30. Not yet hand-reviewed by PLOBT.How this works →

Insulin glulisine

FDA approved · Rx

Rapid-acting insulin analog

Also known as: Apidra, Apidra Solostar

Evidence score
92/ 100
Strong evidence

Strong, human-grade evidence

  • Regulatory standing. FDA-approved prescription medicine
  • Human trials. Backed by controlled human studies
  • Registered human trials. 117 registered studies on ClinicalTrials.gov, most advanced Phase 4
  • 1 cited source. Includes primary / regulatory sources

Computed with the same four public criteria as every profile. The human-evidence grade on an indexed profile is set automatically and may change when it is hand-reviewed. It is not a safety score, not a purity rating, and not medical advice, and not a claim that this compound treats, cures, or prevents any condition.

What it is

Insulin glulisine is a man-made version of human insulin with two small changes to its amino acid sequence that help it absorb faster after injection. Like the body's own insulin, it lowers blood sugar by helping muscle and fat cells take up glucose and by reducing glucose release from the liver. It is sold under the brand names Apidra and Apidra Solostar.

What the evidence shows

Automatic summaryHuman trials

It is FDA-approved for improving blood sugar control in adults and children with diabetes mellitus, and it is backed by a large body of human research, including 124 registered trials that reach Phase 4 and about 209 published papers. Its main known risk, shared with all insulins, is low blood sugar.

Key facts

FDA approval
Confirmed on openFDA

Registered human trials

Published literature

Sources

Risks, side effects and study doses are only published on hand-reviewed profiles. Want this one reviewed, or spotted something wrong? Tell us.