Last reviewed · How we verify

Romosozumab and Denosumab Cycle Therapy

National Taiwan University Hospital · FDA-approved active Small molecule

Romosozumab and denosumab work sequentially to first stimulate bone formation and then inhibit bone resorption, increasing bone mineral density in osteoporosis.

Romosozumab and denosumab work sequentially to first stimulate bone formation and then inhibit bone resorption, increasing bone mineral density in osteoporosis. Used for Osteoporosis in postmenopausal women at high risk of fracture.

At a glance

Generic nameRomosozumab and Denosumab Cycle Therapy
Also known asCycle therapy group
SponsorNational Taiwan University Hospital
Drug classBone-forming agent and antiresorptive agent combination therapy
TargetSclerostin (romosozumab); RANKL (denosumab)
ModalitySmall molecule
Therapeutic areaBone metabolism / Osteoporosis
PhaseFDA-approved

Mechanism of action

Romosozumab is a sclerostin inhibitor that promotes osteoblast activity and bone formation, while denosumab is a RANKL inhibitor that suppresses osteoclast-mediated bone resorption. The sequential or cyclic administration of these agents leverages their complementary mechanisms to achieve greater improvements in bone density and strength compared to monotherapy.

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

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: