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Amyloidosis clinical trials

View clinical trials related to Amyloidosis.

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NCT ID: NCT00224393 Completed - Clinical trials for Primary Systemic Amyloidosis

Phase II Trial of Enbrel in Patients With Primary Systemic Amyloidosis

Start date: February 2001
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of Enbrel in patients with primary systemic Amyloidosis.

NCT ID: NCT00186407 Completed - Amyloidosis Clinical Trials

Autologous Stem Cell Rescue for Primary Amyloidosis

Start date: April 1998
Phase: Phase 2
Study type: Interventional

To evaluate the role of high dose therapy and autologous hematopoietic cell transplant for amyloidosis.

NCT ID: NCT00166413 Completed - Amyloidosis Clinical Trials

Efficacy of CC-5013 (Revlimid or Lenalidomide) in Patients With Primary Systemic Amyloidosis

Start date: April 2005
Phase: Phase 2
Study type: Interventional

Patients with primary systemic amyloidosis will be treated with CC-5013 (lenalidomide; Revlimid) as a single agent for 3 months. If their disease worsens or does not improve during that time frame dexamethasone will be added to the treatment program.

NCT ID: NCT00112593 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Fludarabine and Total-Body Irradiation Followed By Donor Stem Cell Transplant and Cyclosporine and Mycophenolate Mofetil in Treating HIV-Positive Patients With or Without Cancer

Start date: November 1999
Phase: N/A
Study type: Interventional

This clinical trial studies the side effects and best dose of giving fludarabine and total-body irradiation (TBI) together followed by a donor stem cell transplant and cyclosporine and mycophenolate mofetil in treating human immunodeficiency virus (HIV)-positive patients with or without cancer. Giving low doses of chemotherapy, such as fludarabine, and TBI before a donor bone marrow or peripheral blood stem cell transplant helps stop the growth of cancer or abnormal cells and helps stop the patient's immune system from rejecting the donor's stem cells. The donated stem cells may replace the patient's immune cells and help destroy any remaining cancer cells (graft-versus-tumor effect). Sometimes the transplanted cells from a donor can also make an immune response against the body's normal cells. Giving cyclosporine (CSP) and mycophenolate mofetil (MMF) after the transplant may stop this from happening.

NCT ID: NCT00091260 Completed - Multiple Myeloma Clinical Trials

CC-5013 With or Without Dexamethasone in Treating Patients With Primary Systemic Amyloidosis

Start date: January 2004
Phase: Phase 2
Study type: Interventional

RATIONALE: Drugs such as CC-5013 and dexamethasone may be effective in treating primary systemic amyloidosis. PURPOSE: This phase II trial is studying CC-5013 to see how well it works with or without dexamethasone in treating patients with primary systemic amyloidosis.

NCT ID: NCT00089167 Completed - Clinical trials for Multiple Myeloma and Plasma Cell Neoplasm

Melphalan, Thalidomide, and Dexamethasone in Treating Patients With Newly Diagnosed, Previously Untreated Primary Systemic Amyloidosis

Start date: May 2002
Phase: Phase 2
Study type: Interventional

RATIONALE: Drugs such as melphalan, thalidomide, and dexamethasone may be effective in treating patients with primary systemic amyloidosis. PURPOSE: This phase II trial is studying how well giving melphalan together with thalidomide and dexamethasone works in treating patients with primary systemic amyloidosis.

NCT ID: NCT00075621 Completed - Multiple Myeloma Clinical Trials

Tandem Autologous Stem Cell Transplantation in Treating Patients With Primary Systemic (AL) Amyloidosis

Start date: August 2000
Phase: Phase 2
Study type: Interventional

RATIONALE: Autologous stem cell transplantation may be effective treatment for primary systemic (AL) amyloidosis. PURPOSE: This phase II trial is studying how well tandem (two) autologous stem cell transplantation works in treating patients with primary systemic (AL) amyloidosis.

NCT ID: NCT00075608 Completed - Clinical trials for Multiple Myeloma and Plasma Cell Neoplasm

Second Autologous Stem Cell Transplant in Treating Patients With Persistent or Recurrent Primary Systemic (AL) Amyloidosis

Start date: August 2001
Phase: Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of plasma cells, either by killing the cells or by stopping them from dividing. Having a stem cell transplant to replace the blood-forming cells destroyed by chemotherapy, allows higher doses of chemotherapy to be given so that more plasma cells are killed. By reducing the number of plasma cells, the disease may progress more slowly. PURPOSE: This phase II trial is studying how well autologous stem cell transplant works in treating patients with persistent or recurrent primary systemic (AL) amyloidosis.

NCT ID: NCT00064337 Completed - Multiple Myeloma Clinical Trials

S0115, High-Dose Melphalan and Autologous Peripheral Stem Cell Transplantation in Treating Patients With Multiple Myeloma or Primary Systemic Amyloidosis

Start date: January 2004
Phase: Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy such as melphalan work in different ways to stop cancer cells from dividing so they stop growing or die. Combining chemotherapy with donor peripheral stem cell transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more cancer cells. PURPOSE: This phase II trial is studying how well giving melphalan together with autologous stem cell transplantation works in treating patients with multiple myeloma or primary systemic amyloidosis.

NCT ID: NCT00035334 Completed - Clinical trials for Rheumatoid Arthritis

Study of the Safety and Efficacy of NC-503 in Secondary (AA) Amyloidosis

Start date: October 2001
Phase: Phase 2/Phase 3
Study type: Interventional

The main objective of this study is to evaluate the safety and efficacy of NC-503 compared to placebo in patients with secondary (AA) amyloidosis using a composite assessment of clinical improvement/worsening of both renal and gastrointestinal functions.