- Trials with a EudraCT protocol (2,820)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
2,820 result(s) found.
Displaying page 76 of 141.
EudraCT Number: 2007-003348-31 | Sponsor Protocol Number: 2007/311 | Start Date*: 2008-05-15 |
Sponsor Name:Department of Woman and Child health, Karolinska University Hospital | ||
Full Title: Progesterone at imminent premature birth Progesteron vid hotande förtidsbörd | ||
Medical condition: In this randomised, placebo-controlled pilot study the treatment group (n=30) will recieve a daily application of vaginal gel containing progesterone 90 mg/dose (Crinone, Seronomerck) until rupture... | ||
Disease: | ||
Population Age: In utero, Preterm newborn infants, Newborns, Infants and toddlers, Under 18, Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004491-22 | Sponsor Protocol Number: LIFE-PC-01 | Start Date*: 2017-09-01 | |||||||||||
Sponsor Name:Dept. Clinical Medicine, Aarhus Universit | |||||||||||||
Full Title: Early detection of effects of chemotherapy in pancreatic cancer patients – a study using MR-hyperpolarization scanning based on hyperpolarized Pyruvate (13C) injection | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002314-17 | Sponsor Protocol Number: JR-441-101 | Start Date*: 2023-07-03 | |||||||||||
Sponsor Name:JCR Pharmaceuticals Co., Ltd. | |||||||||||||
Full Title: Phase I/II study of weekly infusions of JR-441 in patients with mucopolysaccharidosis type IIIA | |||||||||||||
Medical condition: Mucopolysaccharidosis type IIIA (MPS IIIA) MPS III is an autosomal recessive disease characterized by the accumulation of HS in the tissues throughout the body due to a deficiency in enzymes involv... | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003048-28 | Sponsor Protocol Number: BO44426 | Start Date*: 2023-03-01 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
Full Title: A PHASE Ib/II, OPEN-LABEL, MULTICENTER STUDY EVALUATING THE SAFETY, ACTIVITY, AND PHARMACOKINETICS OF DIVARASIB IN COMBINATION WITH OTHER ANTI-CANCER THERAPIES IN PATIENTS WITH PREVIOUSLY UNTREATED... | ||||||||||||||||||
Medical condition: Untreated Advanced or Metastatic Non-Small Cell Lung Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001635-91 | Sponsor Protocol Number: ODX-MM-001 | Start Date*: 2022-08-10 | |||||||||||
Sponsor Name:DexTech Medical AB | |||||||||||||
Full Title: A Phase I/IIa Study of ODX (OsteoDex) in Multiple Myeloma | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001772-10 | Sponsor Protocol Number: 2016-06 | Start Date*: 2020-02-14 | |||||||||||
Sponsor Name:Assistance Publique-Hôpitaux de Marseille | |||||||||||||
Full Title: Phase I study of oral metronomic NAVELBINE® and HEMANGIOL®combination for children and teenagers with refractory/relapsing solid tumors | |||||||||||||
Medical condition: Pediatric Solid tumor | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004155-16 | Sponsor Protocol Number: CAAA601A42101 | Start Date*: 2022-06-07 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A Phase Ib/II Dose Finding Study Assessing Safety and Efficacy of [177Lu]Lu-DOTA-TATE in Newly Diagnosed Extensive Stage Small Cell Lung Cancer (ES-SCLC) in Combination with Carboplatin, Etoposide ... | |||||||||||||
Medical condition: Extensive-Stage Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002477-26 | Sponsor Protocol Number: NVL-520-01 | Start Date*: 2021-11-26 |
Sponsor Name:Nuvalent, Inc. | ||
Full Title: A Phase 1/2 Study of the Highly Selective ROS1 Inhibitor NVL-520 in Patients with Advanced NSCLC and Other Solid Tumors (ARROS-1) | ||
Medical condition: Advanced Non-Small Cell Lung Cancer (NSCLC)and Other Solid Tumors with ROS1+ rearrangement | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) NL (Ongoing) DE (Ongoing) BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002848-32 | Sponsor Protocol Number: M-2017-322 | Start Date*: 2018-05-15 | |||||||||||||||||||||||||||||||
Sponsor Name:Miltenyi Biomedicine GmbH | |||||||||||||||||||||||||||||||||
Full Title: A phase I/II safety, dose finding and feasibility trial of MB-CART19.1 in patients with relapsed or refractory CD19 positive B cell malignancies. | |||||||||||||||||||||||||||||||||
Medical condition: Pediatric and adult patients with relapsed/refractory (r/r) CD19-expressing B cell acute lymphoblastic leukemia (ALL) and Non-Hodgkin lymphoma (NHL), including chronic lymphocytic leukemia (CLL). | |||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004883-23 | Sponsor Protocol Number: APHP191116 | Start Date*: 2020-10-06 | |||||||||||
Sponsor Name:APHP | |||||||||||||
Full Title: A phase I/II Study evaluating the safety and the efficacy of Human T Lymphoid Progenitor (HTLP) injection to accelerate immune reconstitution after umbilical cord blood (UCB) transplantation in adu... | |||||||||||||
Medical condition: Adult patients (n=10) requiring an allogeneic HSCT for the treatment of AML with an unfavorable prognosis according to international criteria in first complete remission or second complete remissio... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000172-38 | Sponsor Protocol Number: NP137-CT-02 | Start Date*: 2020-09-04 | |||||||||||||||||||||||||||||||
Sponsor Name:NETRIS PHARMA | |||||||||||||||||||||||||||||||||
Full Title: A randomised, multicentre, open label, Phase I/II study to evaluate the safety (Phase I - safety run in), clinical and biological activity (Phase II) of a humanized monoclonal antibody targeting Ne... | |||||||||||||||||||||||||||||||||
Medical condition: Locally advanced/metastatic endometrial carcinoma or cervix carcinoma progressing/relapsing after at least one prior systemic chemotherapy. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000599-38 | Sponsor Protocol Number: RC20_0007 | Start Date*: 2020-11-26 | |||||||||||
Sponsor Name:NANTES CHU | |||||||||||||
Full Title: A phase I/II study to assess the safety, tolerability, pharmacokinetics, pharmacodynamics and efficacy of FR104, a novel antagonist pegylated anti-CD28 Fab’ antibody fragment in de novo renal trans... | |||||||||||||
Medical condition: Kidney transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002814-38 | Sponsor Protocol Number: 69HCL18-0857 | Start Date*: 2019-12-09 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: TROPHAMET, a phase I/II trial of Avelumab and METhotrexate in low-risk gestational TROPHoblastic neoplasias as first line treatment | |||||||||||||
Medical condition: Low-risk gestational trophoblastic neoplasia | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001614-16 | Sponsor Protocol Number: 16TETE04 | Start Date*: 2016-09-22 | |||||||||||
Sponsor Name:INSTITUT CLAUDIUS REGAUD | |||||||||||||
Full Title: A phase I/II multicenter trial evaluating the association of hypofractionated stereotactic radiation therapy and the anti-PD-L1 Durvalumab (Medi4736) for patients with recurrent glioblastoma. | |||||||||||||
Medical condition: Recurrent glioblastoma. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000509-29 | Sponsor Protocol Number: GCT1042-02 | Start Date*: 2022-11-04 | ||||||||||||||||
Sponsor Name:Genmab A/S | ||||||||||||||||||
Full Title: A Phase 1/2, Randomized, Open-Label Trial to Evaluate the Safety and Clinical Activity of Immunoradiotherapy Combinations as a Treatment Option for Subjects With Metastatic Solid Tumors | ||||||||||||||||||
Medical condition: Metastatic Solid Malignant tumors | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002996-36 | Sponsor Protocol Number: 15TETE04 | Start Date*: 2021-06-23 | ||||||||||||||||
Sponsor Name:INSTITUT CLAUDIUS REGAUD | ||||||||||||||||||
Full Title: A Phase I Clinical Study Evaluating the Safety of Peptide Receptor Radionuclide Therapy (PRRT) with 177Lu-DOTA0-Tyr3-Octreotate in Children with Refractory or Recurrent Neuroblastoma expressing som... | ||||||||||||||||||
Medical condition: Recurrent or refractory neuroblastoma. | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003579-31 | Sponsor Protocol Number: N/2014/68 | Start Date*: 2016-01-20 |
Sponsor Name:Centre Hospitalier Régional Universitaire de Besançon | ||
Full Title: PHASE I/II DE RADIOCHIMIOTHERAPIE DANS LES CANCERS DE L’ŒSOPHAGE DU SUJET AGE. OSAGE | ||
Medical condition: Patient âgé de 75 ans et plus porteurs d'un cancer de l'oesophage non opérable et avec une maladie localisée | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004808-60 | Sponsor Protocol Number: HD-CAR-1/V04 | Start Date*: 2018-04-12 | ||||||||||||||||
Sponsor Name:University Hospital Heidelberg | ||||||||||||||||||
Full Title: Treatment of patients with relapsed or refractory CD19+ lymphoid disease with T lymphocytes transduced by RV-SFG.CD19.CD28.4-1BBzeta retroviral vector - A unicenter Phase I /II clinical trial | ||||||||||||||||||
Medical condition: Relapsed and/or refractory CD19+ leukemia and lymphoma | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003215-63 | Sponsor Protocol Number: 69HCL19_0032 | Start Date*: 2020-03-10 | |||||||||||
Sponsor Name:Hospices Civils de Lyon - Direction de la Recherche Clinique et de l'Innovation | |||||||||||||
Full Title: Cultured Autologous Oral Mucosa Epithelial sheet for the Treatment of Bilateral Limbal Stem Cell Deficiency - FEMJA for « Feuillet Epithélial de Muqueuse Jugale Autologue » | |||||||||||||
Medical condition: Bilateral Limbal Stem Cell Deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001385-35 | Sponsor Protocol Number: EXS21546-002 | Start Date*: 2022-11-25 | ||||||||||||||||
Sponsor Name:Exscientia AI Limited | ||||||||||||||||||
Full Title: A phase 1b/2a study to assess the safety, tolerability, pharmacokinetic and anti-tumoural activity of EXS21546 in combination with PD-1 inhibitor in patients with advanced solid tumours. | ||||||||||||||||||
Medical condition: Solid advanced tumours | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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