Osteoporosis
Recent clinical, regulatory, research and industry developments relating to this disease.
GLP-1R Actions on Muscle and the Skeleton
Association Between Low Bone Density, Vertebral Fractures, and Pain in Sickle Cell Disease
Gut microbiota and microbial metabolites for osteoporosis.
Associations Among Estrogens, the Gut Microbiome and Osteoporosis.
Market withdrawal: Zoledronic Acid Hospira (EMA)
Insights and implications of sexual dimorphism in osteoporosis.
Gut microbiota impacts bone via Bacteroides vulgatus-valeric acid-related pathways.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
- 1 regulatory approval from EMA on record.
- 5 clinical trials expected to report results, the earliest in Q2 2027.
- 1 industry development reported.
- Q2 2027A Phase 4 Single-arm Open-label Study for the Efficacy and Safety of Prolia® in Participants With Glucocorticoid-induced Osteoporosis in Mainland China
- Q4 2027Anabolic Therapy in Postmenopausal Osteoporosis
- Q2 2029Effects of Cycle Therapy With Romosozumab and Denosumab 2 Years vs 1 Year Romosozumab Followed by 1 Year Denosumab in Postmenopausal Osteoporosis Patients-A Randomized Control Trial
- Q3 2030The Optimised Use of Romozosumab Study
- Q4 2030StrAtegies For Zoledronic Acid Post-dEnosumab Discontinuation in Postmenopausal oSTeoporosis
Clinical MilestonesView all 12Hide
- 2026-07-02The Optimised Use of Romozosumab StudyResults expected Q3 2030
- 2026-06-23Effects of Cycle Therapy With Romosozumab and Denosumab 2 Years vs 1 Year Romosozumab Followed by 1 Year Denosumab in Postmenopausal Osteoporosis Patients-A Randomized Control TrialResults expected Q2 2029
- 2026-05-27A Phase 4 Single-arm Open-label Study for the Efficacy and Safety of Prolia® in Participants With Glucocorticoid-induced Osteoporosis in Mainland ChinaResults expected Q2 2027
- 2026-04-15Anabolic Therapy in Postmenopausal OsteoporosisResults expected Q4 2027
- 2025-12-31StrAtegies For Zoledronic Acid Post-dEnosumab Discontinuation in Postmenopausal oSTeoporosisResults expected Q4 2030
- 2026-04-30Romosozumab Versus Denosumab in Patients With Glucocorticoid-induced Osteoporosis: a 2-year Extension Study of a Randomized Controlled TrialCompleted
- 2026-03-04Influence of Dermocorticoids on Bone Mineral Density in Patients With Bullous PemphigoidCompleted
- 2025-12-31The Optimal Long Term Treatment Strategy of Anti-resorptive MedicationsPrimary completion
- 2025-11-14The Optimal Sequential Therapy After Long Term Denosumab TreatmentCompleted
- 2025-10-18An Open-label, Single-arm, Multicenter Phase 4 Study to Evaluate Safety and Tolerability of Romosozumab (EVENITY® ) in Postmenopausal Women in India With Osteoporosis and a High Risk of Fracture.Completed
- 2027-10-01A Randomized, Double-blind, Parallel-group, Active-controlled Study to Compare the Efficacy, Pharmacokinetics, Pharmacodynamics, Safety, and Immunogenicity of MAB-22 Versus Prolia® Sourced From the European Union in Postmenopausal Women With OsteoporosisWithdrawn
- 2026-06-25Effervescent Calcium Magnesium Citrate to Prevent Mineral Metabolism and Renal Complications of Chronic Proton Pump Inhibitor TherapyWithdrawn
Industry & MarketViewHide
- 2026-06-10European Commission Approves CinnaGen’s Zandoriah® (teriparatide biosimilar) for Osteoporosis in AdultsRegulatory news · Fierce Pharma
Regulatory UpdatesViewHide
- 2026-04-27Approval — TeriparatideTeriparatide is indicated in adults. Treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture. In postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated. Treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture.
- 2027-10-01ClinicalA Randomized, Double-blind, Parallel-group, Active-controlled Study to Compare the Efficacy, Pharmacokinetics, Pharmacodynamics, Safety, and Immunogenicity of MAB-22 Versus Prolia® Sourced From the European Union in Postmenopausal Women With OsteoporosisWithdrawn
- 2026-07-02ClinicalThe Optimised Use of Romozosumab StudyResults expected Q3 2030
- 2026-06-25ClinicalEffervescent Calcium Magnesium Citrate to Prevent Mineral Metabolism and Renal Complications of Chronic Proton Pump Inhibitor TherapyWithdrawn
- 2026-06-23ClinicalEffects of Cycle Therapy With Romosozumab and Denosumab 2 Years vs 1 Year Romosozumab Followed by 1 Year Denosumab in Postmenopausal Osteoporosis Patients-A Randomized Control TrialResults expected Q2 2029
- 2026-06-10IndustryEuropean Commission Approves CinnaGen’s Zandoriah® (teriparatide biosimilar) for Osteoporosis in AdultsRegulatory news · Fierce Pharma
- 2026-05-27ClinicalA Phase 4 Single-arm Open-label Study for the Efficacy and Safety of Prolia® in Participants With Glucocorticoid-induced Osteoporosis in Mainland ChinaResults expected Q2 2027
- 2026-04-30ClinicalRomosozumab Versus Denosumab in Patients With Glucocorticoid-induced Osteoporosis: a 2-year Extension Study of a Randomized Controlled TrialCompleted
- 2026-04-27RegulatoryApproval — TeriparatideTeriparatide is indicated in adults. Treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture. In postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated. Treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture.
- 2026-04-15ClinicalAnabolic Therapy in Postmenopausal OsteoporosisResults expected Q4 2027
- 2026-03-04ClinicalInfluence of Dermocorticoids on Bone Mineral Density in Patients With Bullous PemphigoidCompleted
Therapeutic landscape
Therapies with a regulatory footing for this condition, alongside the wider set of agents co-studied with it in the literature.
Approval — Teriparatide is indicated in adults. Treatment of osteoporosis in postmenopausal women an… (2026)
Approval — Treatment of osteoporosis in postmenopausal women at increased risk of fracture. (2022)
Approval — Evenity is indicated in treatment of severe osteoporosis in postmenopausal women at high… (2019)
Clinical trials
The current development programme across all trial phases.
Regulatory timeline
Drug regulatory events matched to this condition by indication — EMA.
European Medicines Agency (CC BY 4.0). Events are matched to this condition by drug indication text — approvals/updates for drugs indicated for it, not disease-specific acts.
Research activity
Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.
Major themes8
- Osteoporosis14
- Gastrointestinal Microbiome5
- Osteoporosis, Postmenopausal4
- Osteoporotic Fractures3
- Bone Resorption2
- Osteogenesis2
- Apoptosis1
- Bibliometrics1
Leading journals6
- Archives of osteoporosis3
- Endocrine reviews2
- Frontiers in endocrinology2
- Gut microbes2
- International journal of molecular sciences2
- BioMed research international1
Leading researchers8
- Borgström F2
- Cooper C2
- Harvey NC2
- Kanis JA2
- Lorentzon M2
- McCloskey EV2
- Norton N2
- Adams LA1
Affiliations (unnormalised)6
- School of Medicine3
- Centre for Metabolic Bone Diseases2
- Mary McKillop Institute for Health Research2
- NIHR Southampton Biomedical Research Centre2
- University of Alabama at Birmingham2
- University of Southampton2
Disease biology
Key proteins & gene products studied in this disease. Number shows shared papers.
Related conditions
Diseases frequently studied alongside this one. Number shows shared papers.
Disease profile
A grounded synthesis of the condition — overview, causes, mechanism, risk factors and current standard of care.
Osteoporosis is a reduction in bone mass without a change in bone composition, which weakens the skeleton and leads to fractures. Primary osteoporosis is commonly described as postmenopausal osteoporosis or age-related (senile) osteoporosis.
Primary osteoporosis is associated with postmenopausal estrogen deficiency and with age-related bone loss. The grounding also supports a broader model in which derangements in bone cell birth and death, including osteoclast and osteoblast turnover, contribute to the disease.
The disease reflects impaired bone homeostasis, with reduced bone mass arising from imbalance in bone remodeling. The literature grounding links osteoporosis to altered osteoclast and osteoblast genesis and apoptosis, changes in bone density, and regulatory effects of cytokines, hormones, and signal transduction pathways.
Female sex characteristics and the menopausal transition are supported risk factors through estrogen deficiency. Aging is also a major risk factor, and the grounding additionally points to diet and gastrointestinal microbiome-related factors as areas studied in relation to osteoporosis.
General management includes prevention, diagnosis, and therapy, with treatment described at the level of drug therapy and non-drug prevention and control. The grounding supports estrogen-based therapy as a relevant modality and broader osteoporosis treatment approaches aimed at preserving bone mass and reducing fracture risk.
AI-generated summary grounded in MeSH and 6 peer-reviewed sources. Informational only — not medical advice. Generated 2026-07-07.
Reference
Authoritative identity, definition & identifiers.
Reduction of bone mass without alteration in the composition of bone, leading to fractures. Primary osteoporosis can be of two major types: postmenopausal osteoporosis (OSTEOPOROSIS, POSTMENOPAUSAL) and age-related or senile osteoporosis.
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
- Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
- Related entities are derived from literature co-mention (studied together) — associative, not causal.