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Last Updated: December 23, 2024

CLINICAL TRIALS PROFILE FOR FOSAMAX PLUS D


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All Clinical Trials for FOSAMAX PLUS D

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00000400 ↗ Alendronate and/or Parathyroid Hormone for Osteoporosis Completed National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) Phase 2 1999-08-01 This study looks at the effects of two medications, alendronate and parathyroid hormone, on bone mass and on bone formation and bone breakdown in women with osteoporosis. We will randomly select postmenopausal women who have osteoporosis to receive laboratory-produced human parathyroid hormone (hPTH), or alendronate, or both for 2.5 years. Study participants will return to the study center periodically to have their bone mass measured and to give blood and urine samples for tests of bone formation and breakdown and for other laboratory tests. Those who complete the study are eligible for one or two 12 month extension studies.
NCT00000400 ↗ Alendronate and/or Parathyroid Hormone for Osteoporosis Completed Massachusetts General Hospital Phase 2 1999-08-01 This study looks at the effects of two medications, alendronate and parathyroid hormone, on bone mass and on bone formation and bone breakdown in women with osteoporosis. We will randomly select postmenopausal women who have osteoporosis to receive laboratory-produced human parathyroid hormone (hPTH), or alendronate, or both for 2.5 years. Study participants will return to the study center periodically to have their bone mass measured and to give blood and urine samples for tests of bone formation and breakdown and for other laboratory tests. Those who complete the study are eligible for one or two 12 month extension studies.
NCT00000412 ↗ Osteoporosis Prevention After Heart Transplant Completed Merck Sharp & Dohme Corp. Phase 3 1997-09-01 During the first year after a heart transplant, people often rapidly lose bone from their spine and hips. About 35 percent of people who receive heart transplants will suffer broken bones during the first year after transplantation. This study will compare the safety and effectiveness of the drug alendronate (Fosamax) and the active form of vitamin D (calcitriol) in preventing bone loss at the spine and hip after a heart transplant. In this study, people who have had a successful heart transplant will receive either active alendronate and a "dummy pill" instead of calcitriol, or active calcitriol and a dummy pill instead of alendronate for the first year after their transplant, starting within 1 month after transplant surgery. We will measure bone density in the hip and spine at the start of the study and after 6 and 12 months, and will also check for broken bones in the spine. This research should lead to ways of preventing this crippling form of osteoporosis.
NCT00000412 ↗ Osteoporosis Prevention After Heart Transplant Completed National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) Phase 3 1997-09-01 During the first year after a heart transplant, people often rapidly lose bone from their spine and hips. About 35 percent of people who receive heart transplants will suffer broken bones during the first year after transplantation. This study will compare the safety and effectiveness of the drug alendronate (Fosamax) and the active form of vitamin D (calcitriol) in preventing bone loss at the spine and hip after a heart transplant. In this study, people who have had a successful heart transplant will receive either active alendronate and a "dummy pill" instead of calcitriol, or active calcitriol and a dummy pill instead of alendronate for the first year after their transplant, starting within 1 month after transplant surgery. We will measure bone density in the hip and spine at the start of the study and after 6 and 12 months, and will also check for broken bones in the spine. This research should lead to ways of preventing this crippling form of osteoporosis.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for FOSAMAX PLUS D

Condition Name

Condition Name for FOSAMAX PLUS D
Intervention Trials
Osteoporosis 34
Healthy 4
Postmenopausal Osteoporosis 3
Osteopenia 3
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Condition MeSH

Condition MeSH for FOSAMAX PLUS D
Intervention Trials
Osteoporosis 44
Osteoporosis, Postmenopausal 10
Bone Diseases, Metabolic 10
Spinal Cord Injuries 3
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Clinical Trial Locations for FOSAMAX PLUS D

Trials by Country

Trials by Country for FOSAMAX PLUS D
Location Trials
United States 59
Canada 11
Brazil 10
Mexico 6
Spain 6
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Trials by US State

Trials by US State for FOSAMAX PLUS D
Location Trials
New York 7
Massachusetts 6
California 5
Illinois 5
Maryland 4
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Clinical Trial Progress for FOSAMAX PLUS D

Clinical Trial Phase

Clinical Trial Phase for FOSAMAX PLUS D
Clinical Trial Phase Trials
Phase 4 18
Phase 3 14
Phase 2/Phase 3 3
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Clinical Trial Status

Clinical Trial Status for FOSAMAX PLUS D
Clinical Trial Phase Trials
Completed 45
Terminated 6
Unknown status 4
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Clinical Trial Sponsors for FOSAMAX PLUS D

Sponsor Name

Sponsor Name for FOSAMAX PLUS D
Sponsor Trials
Merck Sharp & Dohme Corp. 13
Amgen 5
Columbia University 4
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Sponsor Type

Sponsor Type for FOSAMAX PLUS D
Sponsor Trials
Other 68
Industry 31
NIH 13
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