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Last Updated: October 15, 2019

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CLINICAL TRIALS PROFILE FOR NEO-MEDROL

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Clinical Trials for Neo-medrol

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00023231 Pediatric Kidney Transplant Without Calcineurin Inhibitors Completed National Institute of Allergy and Infectious Diseases (NIAID) N/A 2001-02-01 The purpose of this study is to see the effect of using drugs other than calcineurin inhibitors to improve the rate of kidney transplant failure. Kidney transplantation can help children with end-stage kidney disease. However, it has been difficult to find treatment for donor graft rejection that does not have a lot of side effects. Researchers hope to find treatments (immunosuppressants) with fewer side effects. One approach is to avoid using calcineurin inhibitors and to try a new drug known as sirolimus instead. Another is to use steroids less often. This study will test whether using sirolimus, fewer steroid treatments, MMF, and certain antibodies will improve long-term graft survival in children receiving kidney transplants from living donors.
NCT00104299 Rituximab for the Treatment of Wegener's Granulomatosis and Microscopic Polyangiitis Completed Genentech, Inc. Phase 2/Phase 3 2005-01-01 Antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis is the most common type of small blood vessel inflammation in adults. ANCA-associated vasculitis includes Wegener's granulomatosis (WG) and microscopic polyangiitis (MPA). Rituximab is a man-made antibody used to treat certain types of cancer. The purpose of this study is to determine the effectiveness of rituximab in treating patients with WG and MPA. Study hypothesis: Rituximab is not inferior to conventional therapy in its ability to induce disease remission by Month 6.
NCT00104299 Rituximab for the Treatment of Wegener's Granulomatosis and Microscopic Polyangiitis Completed Immune Tolerance Network (ITN) Phase 2/Phase 3 2005-01-01 Antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis is the most common type of small blood vessel inflammation in adults. ANCA-associated vasculitis includes Wegener's granulomatosis (WG) and microscopic polyangiitis (MPA). Rituximab is a man-made antibody used to treat certain types of cancer. The purpose of this study is to determine the effectiveness of rituximab in treating patients with WG and MPA. Study hypothesis: Rituximab is not inferior to conventional therapy in its ability to induce disease remission by Month 6.
NCT00104299 Rituximab for the Treatment of Wegener's Granulomatosis and Microscopic Polyangiitis Completed National Institute of Allergy and Infectious Diseases (NIAID) Phase 2/Phase 3 2005-01-01 Antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis is the most common type of small blood vessel inflammation in adults. ANCA-associated vasculitis includes Wegener's granulomatosis (WG) and microscopic polyangiitis (MPA). Rituximab is a man-made antibody used to treat certain types of cancer. The purpose of this study is to determine the effectiveness of rituximab in treating patients with WG and MPA. Study hypothesis: Rituximab is not inferior to conventional therapy in its ability to induce disease remission by Month 6.
NCT00241982 Long-Circulating Liposomal Prednisolone Versus Pulse Intramuscular Methylprednisolone in Patients With Active Rheumatoid Arthritis Completed Utrecht University Phase 2 2005-10-01 Trial to study the safety of a single, intravenous administration of long-circulating liposomal prednisolone disodium phosphate in patients with active rheumatoid arthritis.
NCT00241982 Long-Circulating Liposomal Prednisolone Versus Pulse Intramuscular Methylprednisolone in Patients With Active Rheumatoid Arthritis Completed Radboud University Phase 2 2005-10-01 Trial to study the safety of a single, intravenous administration of long-circulating liposomal prednisolone disodium phosphate in patients with active rheumatoid arthritis.
NCT00279903 Is Botox Effective in Relieving Pain From Knee Osteoarthritis? Completed Mayo Clinic Phase 1 2005-11-01 Patients with painful knee osteoarthritis will be randomly allocated to one of three groups. Each group will receive a knee injection of: 1) cortisone, 2) low dose Botox, or 3) high dose Botox. Patients will then be followed for 6 months to see if they have significant pain relief or improvement in their activity level after the injection.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Neo-medrol

Condition Name

Condition Name for Neo-medrol
Intervention Trials
Osteoarthrosis 6
Leukemia 5
Rheumatoid Arthritis 3
Focal Segmental Glomerulosclerosis (FSGS) 1
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Condition MeSH

Condition MeSH for Neo-medrol
Intervention Trials
Osteoarthritis 10
Joint Diseases 6
Precursor Cell Lymphoblastic Leukemia-Lymphoma 5
Leukemia, Lymphoid 5
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Clinical Trial Locations for Neo-medrol

Trials by Country

Trials by Country for Neo-medrol
Location Trials
United States 33
Denmark 9
India 3
Netherlands 2
Belgium 2
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Trials by US State

Trials by US State for Neo-medrol
Location Trials
Texas 6
New York 3
Maryland 3
Indiana 3
Illinois 2
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Clinical Trial Progress for Neo-medrol

Clinical Trial Phase

Clinical Trial Phase for Neo-medrol
Clinical Trial Phase Trials
Phase 4 5
Phase 3 11
Phase 2/Phase 3 4
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Clinical Trial Status

Clinical Trial Status for Neo-medrol
Clinical Trial Phase Trials
Recruiting 14
Completed 14
Unknown status 6
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Clinical Trial Sponsors for Neo-medrol

Sponsor Name

Sponsor Name for Neo-medrol
Sponsor Trials
Bispebjerg Hospital 7
Rigshospitalet, Denmark 6
M.D. Anderson Cancer Center 5
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Sponsor Type

Sponsor Type for Neo-medrol
Sponsor Trials
Other 52
Industry 16
NIH 4
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