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Therapeutic Area

Osteoporosis

Therapeutic area intelligence for Osteoporosis with 9 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
9
Catalysts
0
Companies
4

Companies

Amgen →
Aurobindo Pharma →
Eli Lilly →
Teva →

Assets

Abaloparatide →
ALMAJECT →
Alvogen →
Aurobindo →
FDA →
FORTEO →
Prolia →
RADIUS →

Recent signals(9)

Regulatory
August 6, 2026

FDA Accepts Supplemental Application for TYMLOS (Abaloparatide)

The FDA has accepted a supplemental application for TYMLOS (abaloparatide) from RADIUS.

RegulatoryAugust 6, 2026

FDA Accepts Supplement Application for Teriparatide by ALMAJECT

The FDA has accepted a supplemental application for Teriparatide submitted by ALMAJECT.

RegulatoryAugust 6, 2026

FDA Accepts Supplemental Application for FORTEO (Teriparatide) by Lilly

The FDA has accepted a supplemental application for FORTEO, a treatment for osteoporosis, submitted by Lilly.

RegulatoryAugust 6, 2026

FDA Accepts Supplemental Application for BONSITY (Teriparatide)

The FDA has accepted a supplemental application for BONSITY, a teriparatide product from Alvogen.

StrategyJuly 27, 2026

Aurobindo Pharma's Alendronate Sodium Supplement Application Approved by FDA

The FDA has approved the supplemental application ANDA090124 for Alendronate Sodium submitted by Aurobindo Pharma.

ClinicalJuly 26, 2026

Clinical Trial on Abaloparatide's Impact on Bone Quality in Osteoporotic Patients

A clinical trial is assessing the efficacy of abaloparatide in improving bone density and reducing postoperative complications in osteoporotic patients undergoing spinal surgery.

ClinicalJuly 25, 2026

Study on Resistance Training Intensity for Osteoporosis Management

A study is underway to evaluate the effects of different resistance training intensities on bone health in individuals with low bone mineral density.

RegulatoryJune 27, 2026

FDA Submission Update for Prolia (Denosumab) by Amgen

Amgen has submitted a supplemental application for Prolia (denosumab) under BLA125320 with standard review priority.

RegulatoryJune 23, 2026

FDA Grants AP Status for Teva's Risedronate Sodium Supplement

Teva Pharmaceuticals has received an Abbreviated Approval (AP) for a supplement of Risedronate Sodium.

Upcoming catalysts

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Indications

No related entities indexed yet.

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