- Trials with a EudraCT protocol (16)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
16 result(s) found for: Immunomedics.
Displaying page 1 of 1.
EudraCT Number: 2019-004868-22 | Sponsor Protocol Number: IMMU-132-14 | Start Date*: 2020-07-31 | |||||||||||
Sponsor Name:Immunomedics, Inc. | |||||||||||||
Full Title: Open-label Rollover Study to Evaluate Long-Term Safety in Subjects with Metastatic Solid Tumors that are Benefiting from Continuation of Therapy with Sacituzumab Govitecan. | |||||||||||||
Medical condition: Metastatic Solid Tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003019-21 | Sponsor Protocol Number: IMMU-132-05 | Start Date*: 2017-12-14 | ||||||||||||||||||||||||||
Sponsor Name:Immunomedics, Inc. | ||||||||||||||||||||||||||||
Full Title: An International, Multi-Center, Open-Label, Randomized, Phase III Trial of Sacituzumab Govitecan versus Treatment of Physician Choice in Patients with Metastatic Triple-Negative Breast Cancer Who R... | ||||||||||||||||||||||||||||
Medical condition: Relapsed/Refractory Triple-Negative Breast Cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) ES (Prematurely Ended) DE (Completed) GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-001563-21 | Sponsor Protocol Number: IM-T-hLL2-18 | Start Date*: 2005-02-02 |
Sponsor Name:Immunomedics, Inc. | ||
Full Title: A Phase II, Single-Arm Trial of Naked Epratuzumab, an Anti-CD22 Humanized Antibody, in Patients with Waldenström's Macroglobulinemia | ||
Medical condition: Waldenström's Macroglobulinemia (WM) is an uncommon B-cell lymphoproliferative disorder that predominantly involves older patients with a slight male preponderance. WM resembles myeloma and chroni... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004516-21 | Sponsor Protocol Number: IMMU-107-04 | Start Date*: 2014-09-16 | |||||||||||
Sponsor Name:Immunomedics, Inc. | |||||||||||||
Full Title: An International, Multi-Center, Double-Blind, Randomized, Phase III Trial of 90Y-Clivatuzumab Tetraxetan plus Low-Dose Gemcitabine Versus Placebo plus Low-Dose Gemcitabine in Patients with Metastat... | |||||||||||||
Medical condition: Metastatic (Stage IV) Pancreatic Adenocarcinoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) ES (Prematurely Ended) FR (Completed) PL (Prematurely Ended) BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004201-33 | Sponsor Protocol Number: IMMU-132-09 | Start Date*: 2019-08-16 | |||||||||||||||||||||
Sponsor Name:Immunomedics, Inc. | |||||||||||||||||||||||
Full Title: Phase 3 Study of Sacituzumab Govitecan (IMMU-132) Versus Treatment of Physician's Choice (TPC) in subjects with Hormonal Receptor-Positive (HR+) Human Epidermal Growth Factor Receptor 2 (HER2) Nega... | |||||||||||||||||||||||
Medical condition: Hormonal Receptor-Positive (HR+) Human Epidermal Growth Factor Receptor 2 (HER2) Negative Metastatic Breast Cancer (MBC) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) DE (Completed) NL (Completed) ES (Ongoing) BE (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-003993-16 | Sponsor Protocol Number: IM-T-hPAM4-02 | Start Date*: 2009-04-03 | ||||||||||||||||
Sponsor Name:Immunomedics, Inc. | ||||||||||||||||||
Full Title: A Phase Ib/II Study of Fractionated 90-Y-hPAM4 Plus Gemcitabine in Patients with Previously Untreated Advanced Pancreatic Cancer | ||||||||||||||||||
Medical condition: This is a phase Ib, open-label, dose exploration study of 90-Y-hPAM4 administered as one or more treatment cycles of fractionated radioimmunotherapy in combination with radiosensitizing gemcitabine... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004844-27 | Sponsor Protocol Number: SURE-01 | Start Date*: 2021-06-01 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: SURE-01_An open label, single-arm, phase 2 study of neoadjuvant sacituzumab govitecan, before radical cystectomy, for patients with muscle-invasive bladder cancer who cannot receive or refuse cispl... | |||||||||||||
Medical condition: Muscle-invasive bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004876-16 | Sponsor Protocol Number: SURE-02 | Start Date*: 2021-11-10 | ||||||||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | ||||||||||||||||||
Full Title: SURE-02_An open label, single-arm, phase 2 study of perioperative pembrolizumab plus sacituzumab govitecan for patients with muscle-invasive bladder cancer who cannot receive or refuse cisplatin-ba... | ||||||||||||||||||
Medical condition: muscle-invasive bladder cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000162-30 | Sponsor Protocol Number: 69HCL16_0728 | Start Date*: 2017-03-30 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Place de la scintigraphie au 99mTc-Leukoscan® dans la prise en charge diagnostique des suspicions d’endocardite infectieuse sur matériels | |||||||||||||
Medical condition: sujets adultes présentant une suspicion clinique d’endocardite infectieuse sur valve prothétique ou d’infection sur dispositif implantable cardiaque. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002964-29 | Sponsor Protocol Number: IMMU-132-13 | Start Date*: 2021-10-12 | ||||||||||||||||||||||||||
Sponsor Name:Gilead Sciences Inc | ||||||||||||||||||||||||||||
Full Title: A Randomized Open-Label Phase III Study of Sacituzumab Govitecan Versus Treatment of Physician’s Choice in Subjects with Metastatic or Locally Advanced Unresectable Urothelial Cancer | ||||||||||||||||||||||||||||
Medical condition: Metastatic or Locally Advanced Unresectable Urothelial Cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Trial now transitioned) FR (Trial now transitioned) PT (Completed) BE (Trial now transitioned) AT (Ongoing) IT (Trial now transitioned) IE (Trial now transitioned) HU (Completed) BG (Completed) CZ (Completed) HR (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000434-47 | Sponsor Protocol Number: IM-T-hA20-08 | Start Date*: 2008-07-22 | ||||||||||||||||
Sponsor Name:Immunomedics, Inc. | ||||||||||||||||||
Full Title: A Phase I/II Study of Immunotherapy with Subcutaneous Administered Veltuzumab (hA20) in Patients with CD20+ Non-Hodgkin's Lymphoma or Chronic Lyphocytic Leukemia | ||||||||||||||||||
Medical condition: Non-Hodgkin's Lymphoma and Chronic Lymphocytic Leukemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000705-59 | Sponsor Protocol Number: IMMU-103-03 | Start Date*: 2005-06-07 | |||||||||||
Sponsor Name:Immunomedics, Inc. | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled, Multi-Center Clinical Trial of Epratuzumab in Patients with Acute Severe SLE Flares Excluding the Renal or Neurological Systems | |||||||||||||
Medical condition: Systemic Lupus Erythematosus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Prohibited by CA) ES (Completed) SK (Completed) IT (Prematurely Ended) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004100-35 | Sponsor Protocol Number: GBG102-SASCIA | Start Date*: 2020-10-09 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:GBG Forschungs GmbH | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Phase III postneoadjuvant study evaluating Sacituzumab Govitecan, an Antibody Drug Conjugate in primary HER2-negative breast cancer patients with high relapse risk after standard neoadjuvant treat... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: HER2-negative breast cancer patients with high relapse risk after standard neoadjuvant treatment | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) IE (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) AT (Trial now transitioned) IT (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000706-31 | Sponsor Protocol Number: IMMU-103-04 | Start Date*: 2005-05-13 | |||||||||||
Sponsor Name:Immunomedics, Inc. | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled, Multi-Center Studyof Epratuzumab in Patients with Active Systemic Lupus Erythematosus | |||||||||||||
Medical condition: Systemic Lupus Erythematosus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Prohibited by CA) BE (Completed) IT (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001167-23 | Sponsor Protocol Number: IMMU-132-06 | Start Date*: 2019-03-20 | ||||||||||||||||||||||||||
Sponsor Name:Immunomedics, Inc. | ||||||||||||||||||||||||||||
Full Title: A Phase II Open Label, Study of IMMU-132 in Metastatic Urothelial Cancer After Failure of Platinum-Based Regimen or Anti-PD-1/ PD-L1 Based Immunotherapy | ||||||||||||||||||||||||||||
Medical condition: Histologically documented locally advanced (tumor [T] 4b, any node [N]; or any T, N 2-3) or metastatic (M1, Stage IV) urothelial or non-urothelial carcinoma of the urinary tract predominant | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) GR (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000793-30 | Sponsor Protocol Number: IntReALL-SR-2010 | Start Date*: 2013-10-25 | |||||||||||
Sponsor Name:Charité - University Hospital of Berlin | |||||||||||||
Full Title: International Study for Treatment of Standard Risk Childhood Relapsed ALL 2010 | |||||||||||||
Medical condition: Acute lymphoblastic leukemia (ALL) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) PT (Completed) GB (GB - no longer in EU/EEA) DE (Completed) BE (Completed) AT (Completed) IE (Completed) FI (Completed) DK (Completed) CZ (Completed) IT (Completed) NL (Completed) FR (Completed) PL (Completed) ES (Prematurely Ended) NO (Completed) | |||||||||||||
Trial results: View results |
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