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Generated: February 21, 2019

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CLINICAL TRIALS PROFILE FOR PREDNISONE

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Clinical Trials for Prednisone

Trial ID Title Status Sponsor Phase Summary
NCT00000146 Optic Neuritis Treatment Trial (ONTT) Unknown status National Eye Institute (NEI) Phase 3 To assess the beneficial and adverse effects of corticosteroid treatment for optic neuritis. To determine the natural history of vision in patients who suffer optic neuritis. To identify risk factors for the development of multiple sclerosis in patients with optic neuritis.
NCT00000147 Longitudinal Optic Neuritis Study (LONS) Unknown status National Eye Institute (NEI) N/A To assess the beneficial and adverse effects of corticosteroid treatment for optic neuritis. To determine the natural history of vision in patients who suffer optic neuritis. To identify risk factors for the development of multiple sclerosis in patients with optic neuritis.
NCT00000178 Multicenter Trial of Prednisone in Alzheimer's Disease Completed National Institute on Aging (NIA) Phase 3 This is a randomized placebo controlled, double blind study. Patients who meet eligibility criteria and decide to participate in the study will be randomly assigned to receive either drug treatment or a placebo. Neither the patients nor the participating investigators will know who is receiving the drugs and who is receiving the placebo. Participation involves 15 outpatient clinic visits over a 68 week period. Patients take study medication at varying doses (the maximum dose is 20 mg daily), along with calcium and vitamin supplements.
NCT00000361 Autoimmunity in Inner Ear Disease Terminated National Institute on Deafness and Other Communication Disorders (NIDCD) Phase 3 The purpose of this study is to determine whether prednisone, methotrexate, and cyclophosphamide are effective in the treatment of rapidly progressive sensorineural hearing loss in both ears. This condition is called autoimmune inner ear disease (AIED), because it is thought that the hearing loss is triggered by an autoimmune process. Treatment attempts to suppress or control this process with powerful anti-inflammatory drugs. This is a Phase III, outpatient study. All study participants will be assigned to one of four different groups testing the experimental use of drugs. The study is scheduled to run for 18 months, with a minimum of 11 visits per participant.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Prednisone

Condition Name

Condition Name for Prednisone
Intervention Trials
Prostate Cancer 135
Lymphoma 135
Multiple Myeloma 76
Leukemia 61
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Condition MeSH

Condition MeSH for Prednisone
Intervention Trials
Lymphoma 325
Prostatic Neoplasms 250
Lymphoma, Non-Hodgkin 125
Leukemia 123
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Clinical Trial Locations for Prednisone

Trials by Country

Trials by Country for Prednisone
Location Trials
Canada 587
Brazil 81
Netherlands 78
Belgium 77
Japan 64
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Trials by US State

Trials by US State for Prednisone
Location Trials
California 300
New York 270
Texas 253
Maryland 212
Ohio 201
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Clinical Trial Progress for Prednisone

Clinical Trial Phase

Clinical Trial Phase for Prednisone
Clinical Trial Phase Trials
Phase 4 177
Phase 3 322
Phase 2/Phase 3 51
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Clinical Trial Status

Clinical Trial Status for Prednisone
Clinical Trial Phase Trials
Completed 560
Recruiting 291
Active, not recruiting 180
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Clinical Trial Sponsors for Prednisone

Sponsor Name

Sponsor Name for Prednisone
Sponsor Trials
National Cancer Institute (NCI) 224
M.D. Anderson Cancer Center 51
Sanofi 35
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Sponsor Type

Sponsor Type for Prednisone
Sponsor Trials
Other 1454
Industry 650
NIH 348
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Serving hundreds of leading biopharmaceutical companies globally:

Argus Health
McKinsey
US Department of Justice
Farmers Insurance
Fuji
Colorcon
Teva
Cantor Fitzgerald
Merck

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