- Trials with a EudraCT protocol (17)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
		
	   		
	   		    
                    
                   	
                   	    17 result(s) found for: Pancytopenia.
                    
                
			
   			
		
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| EudraCT Number: 2014-005264-14 | Sponsor Protocol Number: P130103 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: NA | |||||||||||||
| Medical condition: Fanconi Anemia | |||||||||||||
| 
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-002502-31 | Sponsor Protocol Number: RP-L102-0118 | Start Date*: 2018-10-31 | |||||||||||
| Sponsor Name:Rocket Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase II Clinical Trial to Evaluate the Efficacy of the Infusion of Autologous CD34+ Cells Transduced with a Lentiviral Vector Carrying the FANCA Gene (Orphan Drug) in Patients with Fanconi Anemi... | |||||||||||||
| Medical condition: Fanconi anemia (subtype A) | |||||||||||||
| 
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-006100-12 | Sponsor Protocol Number: FANCOLEN-1 | Start Date*: 2013-04-12 | |||||||||||
| Sponsor Name:FUNDACION PARA LA INVESTIGACION BIOMEDICA DEL HOSPITAL UNIVERSITARIO NIÑO JESUS | |||||||||||||
| Full Title: Clinical Trial Phase I / II to evaluate the safety and efficacy of the infusion of autologous CD34+ cells transduced with a lentiviral vector carrying the FANCA gene (orphan drug) for patients with... | |||||||||||||
| Medical condition: Fanconi anemia (Subtype A) | |||||||||||||
| 
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-006197-88 | Sponsor Protocol Number: FANCOSTEM-1 | Start Date*: 2012-03-22 | |||||||||||
| Sponsor Name:Cristina Díaz de Heredia Rubio | |||||||||||||
| Full Title: Clinical Phase II Trial to evaluate efficacy and safety of CD34+ cells mobilization and collection after treatment with plerixafor and filgrastim in patients with Fanconi anemia for subsequent tra... | |||||||||||||
| Medical condition: Fanconi anemia | |||||||||||||
| 
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001603-16 | Sponsor Protocol Number: COLCHI-COVID | Start Date*: 2020-05-06 | |||||||||||
| Sponsor Name:IDIVAL | |||||||||||||
| Full Title: A RANDOMIZATION, MULTICENTRIC, OPEN-LABEL, CONTROLLED, CLINICAL TRIAL TO INVESTIGATE THE EFFECTIVENESS OF EARLY CHOLCHICINE ADMINISTRATION IN PATIENTS OVER 70 YEARS OF AGE WITH HIGH RISK OF DEVELOP... | |||||||||||||
| Medical condition: Adult patients over 70 years of age diagnosed by COVID-19 with outpatient follow-up | |||||||||||||
| 
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000971-26 | Sponsor Protocol Number: RHF-CAELYX-002 | Start Date*: 2016-04-04 | 
| Sponsor Name:Charles University in Prague, Medical Faculty | ||
| Full Title: Liposoms (drug delivery systems) in kinetically guided therapy of ovarian platinum-resistant carcinoma with doxorubicin using plasmafiltration | ||
| Medical condition: Chemotherapy of ovarian platinum-resistant carcinoma | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-000363-40 | Sponsor Protocol Number: 8409032 | Start Date*: 2016-01-07 | |||||||||||
| Sponsor Name:European Society for Blood and Marrow Transplantation | |||||||||||||
| Full Title: A prospective Randomized multicenter study comparing horse Antithymocyte globuline (hATG) + Cyclosporine A (CsA) with or without Eltrombopag as front-line therapy for severe aplastic anemia patients. | |||||||||||||
| Medical condition: Idiopathic (Severe) Aplastic Anemia, a bone marrow failure syndrome which results in the normal hematopoietic tissue completely missing from the bone marrow, accounting for the subsequent pancytope... | |||||||||||||
| 
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004674-17 | Sponsor Protocol Number: NL59901.078.17 | Start Date*: 2017-10-17 | |||||||||||
| Sponsor Name:Princess Máxima Center for Pediatric Oncology | |||||||||||||
| Full Title: A pilot study to test the feasibility, safety and efficacy of the addition of the BiTE antibody Blinatumomab to the Interfant-06 backbone in infants with MLL-rearranged acute lymphoblastic leukemia... | |||||||||||||
| Medical condition: Acute Lymphoblastic Leukemia | |||||||||||||
| 
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) AT (Completed) BE (Completed) DK (Completed) DE (Completed) CZ (Completed) FR (Ongoing) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001689-12 | Sponsor Protocol Number: MHIPS-2020-001 | Start Date*: 2020-04-11 | 
| Sponsor Name:MONTREAL HEART INSTITUTE | ||
| Full Title: COLCHICINA TEST IN THE SARS-COV2 CORONAVIRUS (COLCORONA-COVID-19) | ||
| Medical condition: Men and women over 40 years of age, with a diagnosis of COVID-19 infection and at least one high risk criterion. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) GB (GB - no longer in EU/EEA) FR (Prematurely Ended) GR (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-018373-38 | Sponsor Protocol Number: RG_09-071 | Start Date*: Information not available in EudraCT | 
| Sponsor Name:University of Birmingham | ||
| Full Title: A Phase I trial of figitumumab, an IGF-1R antibody, in children aged 1-12 years old with relapsed/refractory Solid Tumours | ||
| Medical condition: Paediatric patients aged 1-12 years with relapsed / refractory solid tumours. | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-001387-20 | Sponsor Protocol Number: ELA026-CP002 | Start Date*: 2021-10-11 | ||||||||||||||||
| Sponsor Name:Electra Therapeutics, Inc. | ||||||||||||||||||
| Full Title: A Phase 1b, Open-label, Single-arm, Multicenter Study to Evaluate the Safety, Efficacy and Pharmacokinetics of Multiple Doses of ELA026 in Adults and Adolescents with Secondary Hemophagocytic Lymph... | ||||||||||||||||||
| Medical condition: sHLH is a rare and life-threatening inflammatory syndrome characterized by dysregulated immune function. The disease is associated with a massive systemic inflammatory response for which patients r... | ||||||||||||||||||
| 
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-003810-38 | Sponsor Protocol Number: KCP-8602-801 | Start Date*: 2021-12-01 | |||||||||||||||||||||||||||||||
| Sponsor Name:Karyopharm Therapeutics Inc. | |||||||||||||||||||||||||||||||||
| Full Title: Phase 1/2 Open-Label Study of the Safety, Tolerability and Efficacy of the Selective Inhibitor of Nuclear Export (SINE) Compound Eltanexor (KPT-8602) in Patients with Newly Diagnosed and Relapsed/R... | |||||||||||||||||||||||||||||||||
| Medical condition: High-risk primary refractory MDS patients | |||||||||||||||||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: FR (Completed) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2024-000602-14 | Sponsor Protocol Number: CETB115G2201 | Start Date*: 2025-05-28 | |||||||||||
| Sponsor Name:Novartis | |||||||||||||
| Full Title: A non-randomized, open label, multi-center, Phase II study to assess the safety and efficacy of eltrombopag in combination with rabbit anti-thymocyte globulin (r-ATG) and cyclosporine A (CsA) in Ea... | |||||||||||||
| Medical condition: treatment naive severe aplastic anemia | |||||||||||||
| 
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003166-91 | Sponsor Protocol Number: CETB115E2201 | Start Date*: 2019-05-22 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A phase II, open-label, non-controlled, intra-patient dose escalation study to characterize the pharmacokinetics after oral administration of eltrombopag in pediatric patients with refractory, rela... | |||||||||||||
| Medical condition: Refractory, relapsed or treatment naïve severe aplastic anemia (SAA) or recurrent aplastic anemia (AA) | |||||||||||||
| 
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) PT (Completed) NL (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-000252-28 | Sponsor Protocol Number: SHCVOLT1 | Start Date*: 2009-03-13 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A Multi-Centre Prospective Controlled Trial Comparing Calcineurin Inhibitor Monotherapy With Sirolimus Monotherapy in Hepatitis C Infected Patients with Hepatic Fibrosis Following Liver Transplanta... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Patients who have undergone liver transplantation and are infected with Hepatitis C virus. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2018-004179-11 | Sponsor Protocol Number: 2018-4898 | Start Date*: 2019-06-03 | 
| Sponsor Name:Radboudumc | ||
| Full Title: Effectiveness of Somatostatin Analogues in Patients with hereditary hemorrhagic telangiectasia and symptomatic gastrointestinal bleeding, the SAIPAN-trial: a multicenter, randomized, open-label, pa... | ||
| Medical condition: Hereditary hemorrhagic telangiectasia (HHT) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) DE (Ongoing) FR (Completed) IT (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-008198-73 | Sponsor Protocol Number: CR-AIR-004 | Start Date*: 2010-09-09 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Kiadis Pharma Netherlands B.V. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: An open-label, uncontrolled, multicenter, multinational study on the efficacy and safety of administration of donor lymphocytes depleted of alloreactive T-cells (ATIR), through the use of TH9402 an... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Patients with hematologic malignancies who are eligible for an allogeneic stem cell transplantation but without the availability of an (according to the treating physician) suitable matched related... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) GB (Prematurely Ended) NL (Prematurely Ended) BE (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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