- Trials with a EudraCT protocol (128)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
128 result(s) found for: Granulocyte transfusion.
Displaying page 2 of 7.
EudraCT Number: 2021-003157-27 | Sponsor Protocol Number: Sobi.PEGCET-201 | Start Date*: 2021-12-17 | |||||||||||
Sponsor Name:SWEDISH ORPHAN BIOVITRUM AB (PUBL) | |||||||||||||
Full Title: An Open-label, Single-arm, Multicenter Pilot Study to Evaluate the Pharmacokinetics, Pharmacodynamics and Safety of Pegcetacoplan in Patients with Transplant-associated Thrombotic Microangiopathy (... | |||||||||||||
Medical condition: Transplant-Associated Thrombotic Microangiopathy (TA-TMA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) FR (Trial now transitioned) GR (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004899-18 | Sponsor Protocol Number: LUSPLUS | Start Date*: 2021-09-17 | |||||||||||||||||||||
Sponsor Name:GWT-TUD GmbH | |||||||||||||||||||||||
Full Title: A phase IIIb, open-label, single arm study to evaluate the efficacy and safety of luspatercept in patients with lower-risk MDS and ring-sideroblastic phenotype (MDS-RS) | |||||||||||||||||||||||
Medical condition: Lower-risk myelodysplastic syndrome with ring-sideroblastic phenotype (MDS-RS) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004231-23 | Sponsor Protocol Number: 274948 | Start Date*: 2020-05-29 | |||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||
Full Title: Phase IIb randomised clinical trial repurposing ATRA as a stromal targeting agent in a novel drug combination for pancreatic cancer | |||||||||||||
Medical condition: Pancreatic cancer - locally advanced | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001129-15 | Sponsor Protocol Number: CETB115EES03 | Start Date*: 2018-08-10 | |||||||||||
Sponsor Name:Novartis Farmacéutica S.A. | |||||||||||||
Full Title: The ELTION study – A multicenter open-label interventional study of Eltrombopag in patients with poor graft function after allogeneic hematopoietic stem cell transplantation | |||||||||||||
Medical condition: Patients with poor graft function after allogeneic-hematopoietic stem cells transplantation (allo-HSCT). Patients diagnosed with primary or secondary poor graft function (PGF) defined as two or mo... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006629-23 | Sponsor Protocol Number: 61186372GIC2002 | Start Date*: 2022-08-23 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 1b/2, Open-Label Study of Amivantamab Monotherapy and in Addition to Standard-of-Care Chemotherapy in Participants with Advanced or Metastatic Colorectal Cancer | |||||||||||||
Medical condition: Advanced or Metastatic Colorectal Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-005175-78 | Sponsor Protocol Number: SAMSON-II | Start Date*: 2019-10-10 | |||||||||||
Sponsor Name:Prestige BioPharma Limited | |||||||||||||
Full Title: A Randomized, Double-blind, Parallel Group, Equivalence, Multicenter Phase III Trial to Compare the Efficacy, Safety, Pharmacokinetics and Immunogenicity of HD204 to Avastin® in patients with Metas... | |||||||||||||
Medical condition: Non-squamous Non-small Cell Lung Cancer (nsNSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) HU (Completed) GR (Completed) PL (Completed) BG (Completed) LV (Completed) HR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001151-22 | Sponsor Protocol Number: Alesaa | Start Date*: 2007-06-06 | ||||||||||||||||||||||||||
Sponsor Name:UNIVERSITA` DEGLI STUDI DI NAPOLI FEDERICO II | ||||||||||||||||||||||||||||
Full Title: ALEMTUZUMAB AND LOW-DOSE CYCLOSPORINE-A AS ALTERNATIVE IMMUNOSUPPRESSIVE TREATMENT FOR SEVERE APLASTIC ANEMIA (SAA) AND SINGLE-LINEAGE APLASTIC PATIENTS. | ||||||||||||||||||||||||||||
Medical condition: Aplastic anemia and single-lineage bone marrow failure | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004403-14 | Sponsor Protocol Number: BCX9930-203 | Start Date*: 2021-11-11 | |||||||||||
Sponsor Name:BioCryst Pharmaceuticals Inc | |||||||||||||
Full Title: A Randomized, Double-Blind, Multicenter, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy, Safety, and Tolerability of Oral BCX9930 Monotherapy for the Treatment of Paroxysmal Noct... | |||||||||||||
Medical condition: Paroxysmal Nocturnal Hemoglobinuria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) LT (Completed) CZ (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000503-13 | Sponsor Protocol Number: DS7300-127 | Start Date*: 2022-10-14 | |||||||||||
Sponsor Name:Daiichi Sankyo, Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Open-label Study of DS-7300a, a B7-H3 Antibody Drug Conjugate (ADC), in Subjects with Pretreated Extensive-stage Small Cell Lung Cancer (ES-SCLC) | |||||||||||||
Medical condition: Pretreated Extensive-stage Small Cell Lung Cancer (ES-SCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002055-10 | Sponsor Protocol Number: PURE-01 | Start Date*: 2020-07-06 |
Sponsor Name:Fondazione IRCCS Istituto Nazionale dei Tumori | ||
Full Title: PURE-01 – An open label, single-arm, phase 2 study of neoadjuvant pembrolizumab (MK-3475) before cystectomy for patients with muscle-invasive urothelial bladder cancer. | ||
Medical condition: muscle-invasive urothelial bladder cancer | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022890-33 | Sponsor Protocol Number: EQol-MDS | Start Date*: 2010-11-23 | |||||||||||
Sponsor Name:ASSOCIAZIONE QOL-ONE | |||||||||||||
Full Title: Eltrombopag for the treatment of thrombocytopenia due to low- and intermediate risk myelodysplastic syndromes. | |||||||||||||
Medical condition: Adult patients with low or intermediate-1 IPSS risk MDS and thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) FR (Ongoing) SI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004102-27 | Sponsor Protocol Number: SCI-RP-Pan-P2-001 | Start Date*: 2008-02-20 | ||||||||||||||||
Sponsor Name:SciClone Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double Blind, Placebo Controlled, Phase II Study Evaluating the Efficacy and Safety of RP101 in Combination with Gemcitabine Administered as First-Line Treatment to Subjects with Unre... | ||||||||||||||||||
Medical condition: metastatic pancreatic cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Prematurely Ended) ES (Ongoing) NL (Prematurely Ended) DE (Prematurely Ended) GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005724-38 | Sponsor Protocol Number: TL-895-209 | Start Date*: 2022-05-06 | |||||||||||
Sponsor Name:Telios Pharma, Inc. | |||||||||||||
Full Title: An Open-Label, Multicenter, Phase 1b/2 Study of the Safety and Efficacy of TL-895 Combined with Ruxolitinib in Janus associated Kinase Inhibitor (JAKi) Treatment-Naïve Myelofibrosis (MF) Subjects a... | |||||||||||||
Medical condition: Janus associated Kinase Inhibitor (JAKi) Treatment-Naïve Myelofibrosis (MF) Subjects and Subjects with MF who have a Suboptimal Response to Ruxolitinib | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) HU (Prematurely Ended) IT (Prematurely Ended) ES (Prematurely Ended) DE (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000743-31 | Sponsor Protocol Number: 73841937NSC3003 | Start Date*: 2020-09-23 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 3, Randomized Study of Amivantamab and Lazertinib Combination Therapy Versus Osimertinib Versus Lazertinib as First-Line Treatment in Patients with EGFR Mutated Locally Advanced or Metastat... | |||||||||||||
Medical condition: EGFR-mutated locally advanced or metastatic Non Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) GB (GB - no longer in EU/EEA) DE (Trial now transitioned) PT (Trial now transitioned) HU (Trial now transitioned) PL (Trial now transitioned) NL (Ongoing) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001141-41 | Sponsor Protocol Number: 08-C-0007 | Start Date*: 2012-09-18 | |||||||||||
Sponsor Name:National Cancer Institute NCI | |||||||||||||
Full Title: A PHASE I STUDY OF IPILIMUMAB (ANTI-CTLA-4) IN CHILDREN, ADOLESCENTS, AND YOUNG ADULTS WITH TREATMENT REFRACTORY CANCER | |||||||||||||
Medical condition: Sarcoma - Wilm's Tumor - Lymphoma - Neuroblastoma | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004138-13 | Sponsor Protocol Number: 4976 | Start Date*: 2019-10-16 | |||||||||||
Sponsor Name:THE ROYAL MARSDEN NHS FOUNDATION | |||||||||||||
Full Title: A multicentre phase II non-randomised trial assessing the efficacy of DKN-01 plus atezolizumab in patients with advanced mismatch repair proficient oesophagogastric cancer | |||||||||||||
Medical condition: Patients with advanced mismatch repair proficient oesophagogastric cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001599-31 | Sponsor Protocol Number: N16INM | Start Date*: 2016-08-25 | |||||||||||
Sponsor Name:Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | |||||||||||||
Full Title: Ipilimumab and Nivolumab in the Treatment of malignant Pleural Mesothelioma: a Phase II study | |||||||||||||
Medical condition: Malignant pleural mesothelioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004223-16 | Sponsor Protocol Number: PEBBLE | Start Date*: 2021-05-10 | |||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||
Full Title: A phase II study investigating preoperative bintrafusp alfa in operable urothelial carcinoma of the bladder. | |||||||||||||
Medical condition: Urothelial carcinoma requiring radical cystectomy with bilateral pelvic lymph node dissection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005214-21 | Sponsor Protocol Number: RuNiC. | Start Date*: 2017-07-17 | |||||||||||
Sponsor Name: Grupo Español de Enfermedades Mieloproliferativas GEMFIN | |||||||||||||
Full Title: Phase Ib/II clinical trial of ruxolitinib in combination with nilotinib and prednisona for myelofibrosis: RuNiC study | |||||||||||||
Medical condition: Myeloproliferative Diseases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005392-39 | Sponsor Protocol Number: 213357 | Start Date*: 2022-02-25 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline, S.A. | ||||||||||||||||||
Full Title: OPAL Master Protocol: A Phase 1B/2 Multicohort Umbrella Study to Evaluate the Safety and Efficacy of Novel Treatments and/or Combinations of Treatments in Participants with Ovarian Cancer (OPAL). C... | ||||||||||||||||||
Medical condition: Ovarian cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: ES (Ongoing) DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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