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Last Updated: March 29, 2024

CLINICAL TRIALS PROFILE FOR RHO (D) IMMUNE GLOBULIN


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Biosimilar Clinical Trials for rho (d) immune globulin

This table shows clinical trials for biosimilars. See the next table for all clinical trials
Trial ID Title Status Sponsor Phase Start Date Summary
NCT01624805 ↗ Methylprednisolone, Horse Anti-Thymocyte Globulin, Cyclosporine, Filgrastim, and/or Pegfilgrastim or Pegfilgrastim Biosimilar in Treating Patients With Aplastic Anemia or Low or Intermediate-Risk Myelodysplastic Syndrome Recruiting National Cancer Institute (NCI) Phase 2 2012-06-25 This phase II trial studies methylprednisolone, horse anti-thymocyte globulin, cyclosporine, filgrastim, and/or pegfilgrastim or pegfilgrastim biosimilar in treating patients with aplastic anemia or low or intermediate-risk myelodysplastic syndrome. Horse anti-thymocyte globulin is made from horse blood and targets immune cells known as T-lymphocytes. Since T-lymphocytes are believed to be involved in causing low blood counts in aplastic anemia and in some cases of myelodysplastic syndromes, killing these cells may help treat the disease. Methylprednisolone and cyclosporine work to suppress immune cells called lymphocytes. This may help to improve low blood counts in aplastic anemia and myelodysplastic syndromes. Filgrastim and pegfilgrastim are designed to cause white blood cells to grow. This may help to fight infections and help improve the white blood cell count. Giving methylprednisolone and horse anti-thymocyte globulin together with cyclosporine, filgrastim, and/or pegfilgrastim may be an effective treatment for patients with aplastic anemia or myelodysplastic syndrome.
NCT01624805 ↗ Methylprednisolone, Horse Anti-Thymocyte Globulin, Cyclosporine, Filgrastim, and/or Pegfilgrastim or Pegfilgrastim Biosimilar in Treating Patients With Aplastic Anemia or Low or Intermediate-Risk Myelodysplastic Syndrome Recruiting M.D. Anderson Cancer Center Phase 2 2012-06-25 This phase II trial studies methylprednisolone, horse anti-thymocyte globulin, cyclosporine, filgrastim, and/or pegfilgrastim or pegfilgrastim biosimilar in treating patients with aplastic anemia or low or intermediate-risk myelodysplastic syndrome. Horse anti-thymocyte globulin is made from horse blood and targets immune cells known as T-lymphocytes. Since T-lymphocytes are believed to be involved in causing low blood counts in aplastic anemia and in some cases of myelodysplastic syndromes, killing these cells may help treat the disease. Methylprednisolone and cyclosporine work to suppress immune cells called lymphocytes. This may help to improve low blood counts in aplastic anemia and myelodysplastic syndromes. Filgrastim and pegfilgrastim are designed to cause white blood cells to grow. This may help to fight infections and help improve the white blood cell count. Giving methylprednisolone and horse anti-thymocyte globulin together with cyclosporine, filgrastim, and/or pegfilgrastim may be an effective treatment for patients with aplastic anemia or myelodysplastic syndrome.
>Trial ID >Title >Status >Phase >Start Date >Summary

All Clinical Trials for rho (d) immune globulin

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00000580 ↗ Interruption of Maternal-to-Infant Transmission of Hepatitis B by Means of Hepatitis B Immune Globulin Completed National Heart, Lung, and Blood Institute (NHLBI) Phase 3 1975-11-01 To evaluate whether hepatitis B immune globulin with a high level of antibody against the hepatitis B antigen would be capable of interrupting maternal-fetal transmission of hepatitis B virus, the single most important route of hepatitis spread in the entire Third World.
NCT00000584 ↗ Transfusion-Transmitted Cytomegalovirus Prevention in Neonates Completed National Heart, Lung, and Blood Institute (NHLBI) Phase 3 1983-07-01 To evaluate the capacity of intravenously administered cytomegalovirus (CMV)-immune globin (CMVIG) to immunize high risk premature infants against CMV infections.
NCT00000751 ↗ A Phase III Randomized, Double-Blind, Controlled Study of the Use of Anti-HIV Immune Serum Globulin (HIVIG) for the Prevention of Maternal-Fetal HIV Transmission in Pregnant Women and Newborns Receiving Zidovudine (AZT) Completed National Institute of Allergy and Infectious Diseases (NIAID) Phase 3 1969-12-31 To evaluate the effect of anti-HIV immune serum globulin (HIVIG) versus immune globulin (IVIG) administered during pregnancy and to the newborn, in combination with zidovudine (AZT) administered intrapartum and to the newborn, on incidence of HIV infection in infants born to HIV-infected women who received AZT during pregnancy for medical indications. Vertical transmission of HIV from mother to child may occur before, during, or after parturition (via breast-feeding). It is believed that therapy administered both during pregnancy and intrapartum may help prevent vertical transmission. Additionally, adjunctive short-term antiretroviral therapy for the newborn, following the intensive viral exposure presumed to occur at birth, may be necessary.
NCT00000751 ↗ A Phase III Randomized, Double-Blind, Controlled Study of the Use of Anti-HIV Immune Serum Globulin (HIVIG) for the Prevention of Maternal-Fetal HIV Transmission in Pregnant Women and Newborns Receiving Zidovudine (AZT) Completed Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) Phase 3 1969-12-31 To evaluate the effect of anti-HIV immune serum globulin (HIVIG) versus immune globulin (IVIG) administered during pregnancy and to the newborn, in combination with zidovudine (AZT) administered intrapartum and to the newborn, on incidence of HIV infection in infants born to HIV-infected women who received AZT during pregnancy for medical indications. Vertical transmission of HIV from mother to child may occur before, during, or after parturition (via breast-feeding). It is believed that therapy administered both during pregnancy and intrapartum may help prevent vertical transmission. Additionally, adjunctive short-term antiretroviral therapy for the newborn, following the intensive viral exposure presumed to occur at birth, may be necessary.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for rho (d) immune globulin

Condition Name

Condition Name for rho (d) immune globulin
Intervention Trials
Leukemia 54
Lymphoma 36
Myelodysplastic Syndromes 30
Multiple Myeloma and Plasma Cell Neoplasm 21
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Condition MeSH

Condition MeSH for rho (d) immune globulin
Intervention Trials
Leukemia 71
Preleukemia 52
Myelodysplastic Syndromes 52
Syndrome 47
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Clinical Trial Locations for rho (d) immune globulin

Trials by Country

Trials by Country for rho (d) immune globulin
Location Trials
United States 635
Canada 44
Germany 21
China 20
France 12
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Trials by US State

Trials by US State for rho (d) immune globulin
Location Trials
California 49
Texas 47
New York 45
Ohio 37
Maryland 35
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Clinical Trial Progress for rho (d) immune globulin

Clinical Trial Phase

Clinical Trial Phase for rho (d) immune globulin
Clinical Trial Phase Trials
Phase 4 19
Phase 3 33
Phase 2/Phase 3 12
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Clinical Trial Status

Clinical Trial Status for rho (d) immune globulin
Clinical Trial Phase Trials
Completed 151
Recruiting 41
Terminated 35
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Clinical Trial Sponsors for rho (d) immune globulin

Sponsor Name

Sponsor Name for rho (d) immune globulin
Sponsor Trials
National Cancer Institute (NCI) 60
M.D. Anderson Cancer Center 23
National Heart, Lung, and Blood Institute (NHLBI) 19
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Sponsor Type

Sponsor Type for rho (d) immune globulin
Sponsor Trials
Other 300
NIH 112
Industry 85
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