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TAK-625

Takeda · Phase 3 active Small molecule

TAK-625 is a GLP-1 receptor agonist Small molecule drug developed by Takeda. It is currently in Phase 3 development for Type 2 diabetes. Also known as: Maralixibat chloride.

TAK-625 is a glucagon-like peptide-1 (GLP-1) receptor agonist.

TAK-625 is a glucagon-like peptide-1 (GLP-1) receptor agonist. Used for Type 2 diabetes.

At a glance

Generic nameTAK-625
Also known asMaralixibat chloride
SponsorTakeda
Drug classGLP-1 receptor agonist
TargetGLP-1R
ModalitySmall molecule
Therapeutic areaDiabetes
PhasePhase 3

Mechanism of action

TAK-625 works by mimicking the action of the natural hormone GLP-1, which helps to lower blood sugar levels by enhancing glucose-dependent insulin secretion, suppressing inappropriately elevated glucagon secretion, and slowing gastric emptying.

Approved indications

Common side effects

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

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Frequently asked questions about TAK-625

What is TAK-625?

TAK-625 is a GLP-1 receptor agonist drug developed by Takeda, indicated for Type 2 diabetes.

How does TAK-625 work?

TAK-625 is a glucagon-like peptide-1 (GLP-1) receptor agonist.

What is TAK-625 used for?

TAK-625 is indicated for Type 2 diabetes.

Who makes TAK-625?

TAK-625 is developed by Takeda (see full Takeda pipeline at /company/takeda).

Is TAK-625 also known as anything else?

TAK-625 is also known as Maralixibat chloride.

What drug class is TAK-625 in?

TAK-625 belongs to the GLP-1 receptor agonist class. See all GLP-1 receptor agonist drugs at /class/glp-1-receptor-agonist.

What development phase is TAK-625 in?

TAK-625 is in Phase 3.

What are the side effects of TAK-625?

Common side effects of TAK-625 include Nausea, Vomiting, Diarrhea, Abdominal pain.

What does TAK-625 target?

TAK-625 targets GLP-1R and is a GLP-1 receptor agonist.

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