Skip to main content
Healing / RecoveryVerified

Teduglutide

Gattex · Revestive · ALX-0600

A GLP-2 analog approved for short bowel syndrome in patients dependent on parenteral support. GLP-2 acts on the intestinal mucosa, a different receptor from the GLP-1 agonists used for metabolic indications.

Teduglutide
Category
Healing / Recovery
Half-life
~2 h in healthy subjects, ~1.3 h in short bowel syndrome, subcutaneous
Common vial
5 mg
Regulatory
FDA approved

Tracking and educational reference only, on values you enter or import yourself. Not medical advice or a dosing recommendation.

01

Regulatory status

FDA approved

The FDA has approved at least one product containing this substance for a specific medical use, which means it has been through the agency review process and carries an approved label. Approval is always for named indications in named populations, so it is not a statement that any other use has been evaluated.

A regulatory status describes paperwork, not safety. An approved compound can still be wrong for a given person, and an unapproved one is neither thereby dangerous nor thereby fine.

02

Half-life

~2 h in healthy subjects, ~1.3 h in short bowel syndrome, subcutaneous. Half-life is an educational pharmacology figure, drawn from public sources, and is not a schedule or dosing instruction.

03

Storage & handling

Supplied as a lyophilized powder in a single-dose vial, reconstituted with the supplied diluent before use.

04

References

  • FDA label: Gattex (NDA 203441)

Read the source

Common questions

Teduglutide, answered plainly.

01What is Teduglutide?+

A GLP-2 analog approved for short bowel syndrome in patients dependent on parenteral support. GLP-2 acts on the intestinal mucosa, a different receptor from the GLP-1 agonists used for metabolic indications. It is also referred to as Gattex, Revestive, ALX-0600. It is listed here under Healing / Recovery as educational reference, which is not a recommendation to use it.

02Is Teduglutide FDA approved?+

FDA approved. The FDA has approved at least one product containing this substance for a specific medical use, which means it has been through the agency review process and carries an approved label. Approval is always for named indications in named populations, so it is not a statement that any other use has been evaluated.

03What is the half-life of Teduglutide?+

~2 h in healthy subjects, ~1.3 h in short bowel syndrome, subcutaneous. A half-life is an educational pharmacology figure describing how long the body takes to clear half of a substance. It is not a schedule and does not imply one.

04How is Teduglutide stored and handled?+

Supplied as a lyophilized powder in a single-dose vial, reconstituted with the supplied diluent before use. Storage conditions come from a manufacturer's own label where one exists, and a compound with no approved label has no agency-reviewed handling instructions at all.

05What vial strengths of Teduglutide are commonly sold?+

Commonly listed vial strengths are 5 mg. A vial strength is a market fact about how a product is packaged. It is not a dose, and it says nothing about how much of anything belongs in any person.

Educational reference only, compiled from public sources. Not medical advice, diagnosis, treatment, or a dosing recommendation, and not a recommendation to use any compound. Many compounds listed are research materials not approved for human use. Consult a qualified professional.