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Alendronate and Zoledronate

National Taiwan University Hospital · FDA-approved active Small molecule

Bisphosphonates that inhibit osteoclast-mediated bone resorption by binding to hydroxyapatite on bone surfaces and reducing osteoclast activity.

Bisphosphonates that inhibit osteoclast-mediated bone resorption by binding to hydroxyapatite on bone surfaces and reducing osteoclast activity. Used for Osteoporosis in postmenopausal women, Osteoporosis in men, Glucocorticoid-induced osteoporosis.

At a glance

Generic nameAlendronate and Zoledronate
SponsorNational Taiwan University Hospital
Drug classBisphosphonate
TargetFarnesyl pyrophosphate synthase (mevalonate pathway); hydroxyapatite binding
ModalitySmall molecule
Therapeutic areaBone metabolism / Osteoporosis
PhaseFDA-approved

Mechanism of action

Alendronate and zoledronate are nitrogen-containing bisphosphonates that accumulate in bone and inhibit farnesyl pyrophosphate synthase in the mevalonate pathway of osteoclasts, leading to osteoclast apoptosis and reduced bone turnover. This mechanism decreases bone resorption and increases bone mineral density, making them effective for treating osteoporosis and other bone loss conditions.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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