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Drug ReportsStrontium ranelate
Strontium ranelate
Osseor, Protelos (strontium ranelate) is a small molecule pharmaceutical. Strontium ranelate was first approved as Protelos on 2004-09-20. It has been approved in Europe to treat postmenopausal osteoporosis.
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Events Timeline
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
musculoskeletal diseasesD009140
nutritional and metabolic diseasesD009750
Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
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Indications
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Agency Specific
FDA
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Patent Expiration
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ATC Codes
M: Musculo-skeletal system drugs
— M05: Drugs for treatment of bone diseases
— M05B: Drugs affecting bone structure and mineralization
— M05BX: Other drugs affecting bone structure and mineralization in atc
— M05BX03: Strontium ranelate
— M05BX53: Strontium ranelate and colecalciferol
HCPCS
No data
Clinical
Clinical Trials
8 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
OsteoporosisD010024HP_0000939M81.0—1—416
Bone fracturesD050723EFO_0003931T14.8———112
Postmenopausal osteoporosisD015663EFO_0003854————2—2
Metabolic bone diseasesD001851HP_0000938————1—1
HyperparathyroidismD006961EFO_0008506E21.3———1—1
Primary hyperparathyroidismD049950EFO_0008519E21.0———1—1
ComplianceD003187—————1—1
Indications Phases 3
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Indications Phases 2
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Indications Phases 1
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Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Knee osteoarthritisD020370EFO_0004616M17————11
OsteoarthritisD010003EFO_0002506M15-M19————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameStrontium ranelate
INN—
Description
Strontium ranelate, a strontium(II) salt of ranelic acid, is a medication for osteoporosis marketed as Protelos or Protos by Servier. Studies indicate it can also slow the course of osteoarthritis of the knee. The drug is unusual in that it both increases deposition of new bone by osteoblasts and reduces the resorption of bone by osteoclasts. It is therefore promoted as a "dual action bone agent" (DABA).
Classification
Small molecule
Drug class—
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Structure (InChI/SMILES or Protein Sequence)
N#Cc1c(N(CC(=O)[O-])CC(=O)[O-])sc(C(=O)[O-])c1CC(=O)[O-].[Sr+2].[Sr+2]
Identifiers
PDB—
CAS-ID135459-87-9
RxCUI—
ChEMBL IDCHEMBL3707306
ChEBI ID—
PubChem CID6918182
DrugBank—
UNII ID—
Target
No data
Variants
No data
Financial
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 2,549 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
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221 adverse events reported
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