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Last Updated: December 12, 2019

DrugPatentWatch Database Preview

CLINICAL TRIALS PROFILE FOR SODIUM FLUORIDE F-18

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505(b)(2) Clinical Trials for Sodium Fluoride F-18

This table shows clinical trials for potential 505(b)(2) applications. See the next table for all clinical trials
Trial Type Trial ID Title Status Sponsor Phase Start Date Summary
OTC NCT03774498 Effect of Different Over-the-counter Toothpastes on Enamel Remineralization Not yet recruiting Cairo University N/A 2019-01-01 This study will be conducted to compare between recent over-the-counter toothpaste (Novamin & Fluoride) and regular over-the-counter toothpaste (Sodium Fluoride) in remineralization potential, so as to be able to know which of the toothpastes will have a better remineralization potential on demineralized enamel.
>Trial Type >Trial ID >Title >Status >Phase >Start Date >Summary

All Clinical Trials for Sodium Fluoride F-18

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00005006 Parathyroid Hormone (PTH) With Alendronate for Osteoporosis Completed National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) Phase 2 1987-09-01 This study investigates the effectiveness of parathyroid hormone (PTH) in combination with alendronate, a standard treatment for osteoporosis that blocks or reduces bone loss. We are using alendronate because it may help protect patients against any possible harmful effects of PTH in cortical bone such as the long bones or hip. We are testing two different treatment schedules of PTH-one in which we give PTH daily and one in which we give PTH for 3 out of every 6 months in a cyclical fashion. The entire study is 21 months long; the active treatment period is 18 months with a 6-month followup period. The main effects we will look for in this study are changes in body chemicals that are signs of bone formation or bone breakdown, and changes in bone density throughout the skeleton. We will randomly assign all study participants, who are women aged 50 and over, to either stay on alendronate alone, receive daily continuous PTH plus alendronate, or receive daily PTH for 3 months out of every 6 for a total of three separate 3-month cycles of PTH plus daily alendronate.
NCT00005006 Parathyroid Hormone (PTH) With Alendronate for Osteoporosis Completed Helen Hayes Hospital Phase 2 1987-09-01 This study investigates the effectiveness of parathyroid hormone (PTH) in combination with alendronate, a standard treatment for osteoporosis that blocks or reduces bone loss. We are using alendronate because it may help protect patients against any possible harmful effects of PTH in cortical bone such as the long bones or hip. We are testing two different treatment schedules of PTH-one in which we give PTH daily and one in which we give PTH for 3 out of every 6 months in a cyclical fashion. The entire study is 21 months long; the active treatment period is 18 months with a 6-month followup period. The main effects we will look for in this study are changes in body chemicals that are signs of bone formation or bone breakdown, and changes in bone density throughout the skeleton. We will randomly assign all study participants, who are women aged 50 and over, to either stay on alendronate alone, receive daily continuous PTH plus alendronate, or receive daily PTH for 3 months out of every 6 for a total of three separate 3-month cycles of PTH plus daily alendronate.
NCT00078026 An Investigation Into the Short Term Effect of APOMINE in Patients With Osteoporosis or Low Bone Mass Terminated Genzyme, a Sanofi Company Phase 1/Phase 2 2003-08-01 Osteoporosis affects millions of postmenopausal women in the USA. The current approved treatments are all drugs that prevent bone loss and possibly result in small gains in bone mass. Another possible treatment consists of drugs that increase bone formation. There are currently two drugs that stimulate bone formation, sodium fluoride and human parathyroid hormone (hPTH). Neither of these two drugs has been approved by the FDA. APOMINE has shown significant bone formation in animal studies. In this study we plan to test whether APOMINE is able to stimulate new bone formation in women with osteoporosis or low bone mass.
NCT00497029 Early Childhood Caries Prevention at a Pediatric Clinic Completed University of Maryland Baltimore Dental School N/A 2004-06-01 This purpose of this study was to evaluate effectiveness of a risk-based dental caries prevention program conducted by dental personnel at an urban pediatric primary care clinic serving largely low-income residents of Baltimore, Maryland, and to appraise this program as a model for similar urban pediatric settings.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Sodium Fluoride F-18

Condition Name

Condition Name for Sodium Fluoride F-18
Intervention Trials
Dental Caries 10
Dentin Sensitivity 6
Early Childhood Caries 4
Dental Plaque 4
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Condition MeSH

Condition MeSH for Sodium Fluoride F-18
Intervention Trials
Dental Caries 15
Prostatic Neoplasms 9
Hypersensitivity 8
Dentin Sensitivity 8
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Clinical Trial Locations for Sodium Fluoride F-18

Trials by Country

Trials by Country for Sodium Fluoride F-18
Location Trials
United States 130
Canada 10
Brazil 9
United Kingdom 5
Egypt 4
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Trials by US State

Trials by US State for Sodium Fluoride F-18
Location Trials
Indiana 13
Maryland 10
New Jersey 6
New York 6
Illinois 5
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Clinical Trial Progress for Sodium Fluoride F-18

Clinical Trial Phase

Clinical Trial Phase for Sodium Fluoride F-18
Clinical Trial Phase Trials
Phase 4 15
Phase 3 15
Phase 2/Phase 3 3
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Clinical Trial Status

Clinical Trial Status for Sodium Fluoride F-18
Clinical Trial Phase Trials
Completed 43
Recruiting 16
Not yet recruiting 10
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Clinical Trial Sponsors for Sodium Fluoride F-18

Sponsor Name

Sponsor Name for Sodium Fluoride F-18
Sponsor Trials
GlaxoSmithKline 15
National Cancer Institute (NCI) 9
Colgate Palmolive 5
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Sponsor Type

Sponsor Type for Sodium Fluoride F-18
Sponsor Trials
Other 58
Industry 36
NIH 12
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