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kallikrein

Techpool Bio-Pharma Co., Ltd. · FDA-approved active Small molecule ✓ Verified May 2026

kallikrein is a Small molecule drug developed by Techpool Bio-Pharma Co., Ltd.. It is currently FDA-approved. Also known as: KLK, Human urinary kallikrein, Human urinary kallidinogenase.

Kallikrein is a subgroup of serine proteases that can cleave peptide bonds in proteins. It has been studied in various clinical trials for conditions such as prostatic neoplasms, acute ischemic stroke, and hereditary angioedema, often in combination with other treatments like docetaxel and prednisone.

At a glance

Generic namekallikrein
Also known asKLK, Human urinary kallikrein, Human urinary kallidinogenase
SponsorTechpool Bio-Pharma Co., Ltd.
ModalitySmall molecule
Therapeutic areaOther
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

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Frequently asked questions about kallikrein

What is kallikrein?

kallikrein is a Small molecule drug developed by Techpool Bio-Pharma Co., Ltd..

Who makes kallikrein?

kallikrein is developed and marketed by Techpool Bio-Pharma Co., Ltd. (see full Techpool Bio-Pharma Co., Ltd. pipeline at /company/techpool-bio-pharma-co-ltd).

Is kallikrein also known as anything else?

kallikrein is also known as KLK, Human urinary kallikrein, Human urinary kallidinogenase.

What development phase is kallikrein in?

kallikrein is FDA-approved (marketed).

Related

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