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teriparatide and raloxifene

Medical University of Vienna · FDA-approved active Small molecule

This combination therapy stimulates bone formation through PTH receptor activation while simultaneously blocking estrogen receptor-mediated bone resorption.

This combination therapy stimulates bone formation through PTH receptor activation while simultaneously blocking estrogen receptor-mediated bone resorption. Used for Osteoporosis in postmenopausal women.

At a glance

Generic nameteriparatide and raloxifene
Also known asForteo, Evista
SponsorMedical University of Vienna
Drug classCombination therapy: PTH analog and selective estrogen receptor modulator (SERM)
TargetPTH1 receptor (teriparatide); estrogen receptor alpha and beta (raloxifene)
ModalitySmall molecule
Therapeutic areaEndocrinology / Bone Metabolism
PhaseFDA-approved

Mechanism of action

Teriparatide is a recombinant parathyroid hormone analog that activates PTH1 receptors on osteoblasts to promote bone formation and increase bone mineral density. Raloxifene is a selective estrogen receptor modulator (SERM) that acts as an estrogen agonist in bone tissue to inhibit osteoclast-mediated bone resorption. Together, they provide complementary anabolic and anti-resorptive effects for enhanced bone strengthening.

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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