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Last Updated: March 29, 2024

CLINICAL TRIALS PROFILE FOR HYDREA


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All Clinical Trials for Hydrea

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00023959 ↗ Bevacizumab, Fluorouracil, and Hydroxyurea Plus Radiation Therapy in Treating Patients With Advanced Head and Neck Cancer Completed National Cancer Institute (NCI) Phase 1 2001-07-01 Monoclonal antibodies, such as bevacizumab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or deliver cancer-killing substances to them. Drugs used in chemotherapy work in different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining monoclonal antibody therapy with chemotherapy and radiation therapy may be an effective treatment for head and neck cancer. This phase I trial is to see if combining bevacizumab, fluorouracil, and hydroxyurea with radiation therapy works in treating patients who have advanced head and neck cancer
NCT00127972 ↗ 2NN & CHARM Long-Term Follow-up Study Completed Boehringer Ingelheim Phase 4 2004-02-01 It is desirable to obtain extended follow up data on subjects who participated in the 2NN study and the CHARM study in order to see if the beneficial effect of using nevirapine continues up to 144 weeks of treatment.
NCT00127972 ↗ 2NN & CHARM Long-Term Follow-up Study Completed International Antiviral Therapy Evaluation Center Phase 4 2004-02-01 It is desirable to obtain extended follow up data on subjects who participated in the 2NN study and the CHARM study in order to see if the beneficial effect of using nevirapine continues up to 144 weeks of treatment.
NCT00336362 ↗ Evaluating the Safety of G-CSF Mobilization in Individuals With Beta Thalassemia Major Completed George Papanicolaou Hospital N/A 2006-07-01 Beta thalassemia major is a serious genetic disease of the blood. Treatments are limited, and although a bone marrow transplant from a compatible donor can be curative, only a limited percentage of individuals with this disease have a matched donor available. A long-term goal of study researchers is to develop a gene transfer process as a method of curing beta thalassemia major. Gene transfer involves obtaining blood stem cells from an individual, adding a normal globin gene to the stem cells, and putting the cells back into the individual. Before gene transfer methods can be attempted in individuals with beta thalassemia major, a safe method of obtaining blood stem cells needs to be developed. The purpose of this study is to investigate the safety and feasibility of collecting peripheral blood stem cells (PBSC) from individuals with beta thalassemia major. Research participants will be given G-CSF (filgrastim) for several days to increase the number of stem cells in the blood, a process called "mobilization." After mobilization, participants will undergo a procedure called apheresis to remove the white blood cells. Researchers in the laboratory will purify the stem cells from the mixture and test methods of putting a normal globin gene into the stem cells. Half of the participants will receive hydroxyurea (HU) prior to G-CSF mobilization. HU is used in splenectomized patients to attempt to reduce the risk of clotting during mobilization. In non-splenectomized patients, HU is given in an attempt to decrease the size of the spleen.
NCT00336362 ↗ Evaluating the Safety of G-CSF Mobilization in Individuals With Beta Thalassemia Major Completed National Heart, Lung, and Blood Institute (NHLBI) N/A 2006-07-01 Beta thalassemia major is a serious genetic disease of the blood. Treatments are limited, and although a bone marrow transplant from a compatible donor can be curative, only a limited percentage of individuals with this disease have a matched donor available. A long-term goal of study researchers is to develop a gene transfer process as a method of curing beta thalassemia major. Gene transfer involves obtaining blood stem cells from an individual, adding a normal globin gene to the stem cells, and putting the cells back into the individual. Before gene transfer methods can be attempted in individuals with beta thalassemia major, a safe method of obtaining blood stem cells needs to be developed. The purpose of this study is to investigate the safety and feasibility of collecting peripheral blood stem cells (PBSC) from individuals with beta thalassemia major. Research participants will be given G-CSF (filgrastim) for several days to increase the number of stem cells in the blood, a process called "mobilization." After mobilization, participants will undergo a procedure called apheresis to remove the white blood cells. Researchers in the laboratory will purify the stem cells from the mixture and test methods of putting a normal globin gene into the stem cells. Half of the participants will receive hydroxyurea (HU) prior to G-CSF mobilization. HU is used in splenectomized patients to attempt to reduce the risk of clotting during mobilization. In non-splenectomized patients, HU is given in an attempt to decrease the size of the spleen.
NCT00336362 ↗ Evaluating the Safety of G-CSF Mobilization in Individuals With Beta Thalassemia Major Completed University of Washington N/A 2006-07-01 Beta thalassemia major is a serious genetic disease of the blood. Treatments are limited, and although a bone marrow transplant from a compatible donor can be curative, only a limited percentage of individuals with this disease have a matched donor available. A long-term goal of study researchers is to develop a gene transfer process as a method of curing beta thalassemia major. Gene transfer involves obtaining blood stem cells from an individual, adding a normal globin gene to the stem cells, and putting the cells back into the individual. Before gene transfer methods can be attempted in individuals with beta thalassemia major, a safe method of obtaining blood stem cells needs to be developed. The purpose of this study is to investigate the safety and feasibility of collecting peripheral blood stem cells (PBSC) from individuals with beta thalassemia major. Research participants will be given G-CSF (filgrastim) for several days to increase the number of stem cells in the blood, a process called "mobilization." After mobilization, participants will undergo a procedure called apheresis to remove the white blood cells. Researchers in the laboratory will purify the stem cells from the mixture and test methods of putting a normal globin gene into the stem cells. Half of the participants will receive hydroxyurea (HU) prior to G-CSF mobilization. HU is used in splenectomized patients to attempt to reduce the risk of clotting during mobilization. In non-splenectomized patients, HU is given in an attempt to decrease the size of the spleen.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Hydrea

Condition Name

Condition Name for Hydrea
Intervention Trials
Sickle Cell Anemia 7
Sickle Cell Disease 6
Stroke 4
Head and Neck Squamous Cell Carcinoma 2
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Condition MeSH

Condition MeSH for Hydrea
Intervention Trials
Anemia, Sickle Cell 11
Anemia 5
Carcinoma 5
Carcinoma, Squamous Cell 5
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Clinical Trial Locations for Hydrea

Trials by Country

Trials by Country for Hydrea
Location Trials
United States 47
Nigeria 4
France 2
Brazil 1
Congo 1
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Trials by US State

Trials by US State for Hydrea
Location Trials
North Carolina 6
Illinois 6
Tennessee 4
Alabama 3
Texas 3
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Clinical Trial Progress for Hydrea

Clinical Trial Phase

Clinical Trial Phase for Hydrea
Clinical Trial Phase Trials
Phase 4 1
Phase 3 5
Phase 2 11
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Clinical Trial Status

Clinical Trial Status for Hydrea
Clinical Trial Phase Trials
Completed 9
Active, not recruiting 6
Terminated 4
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Clinical Trial Sponsors for Hydrea

Sponsor Name

Sponsor Name for Hydrea
Sponsor Trials
National Cancer Institute (NCI) 8
Vanderbilt University Medical Center 4
National Heart, Lung, and Blood Institute (NHLBI) 4
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Sponsor Type

Sponsor Type for Hydrea
Sponsor Trials
Other 83
NIH 17
Industry 4
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