- Trials with a EudraCT protocol (131)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
131 result(s) found for: Gene signature.
Displaying page 6 of 7.
EudraCT Number: 2005-002759-42 | Sponsor Protocol Number: AGLU02704 | Start Date*: 2007-07-18 | |||||||||||
Sponsor Name:Genzyme Europe BV | |||||||||||||
Full Title: A Randomized, Double-Blind, Multicenter, Multinational, Placebo-Controlled Study of the Safety, Efficacy, and Pharmacokinetics of Myozyme, Recombinant Human Acid alpha-Glucosidase (rhGAA), Treatmen... | |||||||||||||
Medical condition: Glycogen Storage Disease type II (Pompe's disease) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001175-31 | Sponsor Protocol Number: ALM201/0001 | Start Date*: 2014-10-10 | ||||||||||||||||
Sponsor Name:Almac Discovery | ||||||||||||||||||
Full Title: A phase I open-label multicentre dose-escalation study of subcutaneous ALM201 in patients with advanced ovarian cancer and other solid tumours. | ||||||||||||||||||
Medical condition: Advanced ovarian cancer and other solid tumours | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-002069-22 | Sponsor Protocol Number: ET17-057 | Start Date*: 2018-04-18 | |||||||||||
Sponsor Name:CENTRE LEON BERARD | |||||||||||||
Full Title: BREASTIMMUNE02 - A multicenter, randomized, open-label, Phase II trial aiming to evaluate the impact of pegfilgrastim on trastuzumab anti-tumor effect and antibody-dependent cell-mediated cytotoxic... | |||||||||||||
Medical condition: Operable HER2 positive breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005605-27 | Sponsor Protocol Number: TNG908-C101 | Start Date*: 2022-09-07 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Tango Therapeutics, Inc. | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG908 in Patients with MTAP-deleted Advanced or Metastatic Solid Tumors | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Phase 1: • Locally advanced or metastatic MTAP-deleted solid tumors (with the exception of gliomas) Phase 2: • Arm 1: Locally advanced or metastatic MTAP-deleted squamous and nonsquamous NSCLC ... | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000252-18 | Sponsor Protocol Number: 35RC20_9803_RePERSO | Start Date*: 2021-04-27 | |||||||||||
Sponsor Name:Rennes University Hospital | |||||||||||||
Full Title: Evaluation of treatment PERSOnalization based on its therapeutic monitoring in patients with metastatic colorectal cancer treated with regorafenib | |||||||||||||
Medical condition: metastatic colorectal cancer | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000528-39 | Sponsor Protocol Number: TAK-676-1002 | Start Date*: 2023-03-20 | |||||||||||
Sponsor Name:Takeda Development Center Americas, Inc. (TDC Americas) | |||||||||||||
Full Title: An Open-label, Dose Escalation, Phase 1/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of TAK-676 as a Single Agent and in Combination With Pembrolizumab in Ad... | |||||||||||||
Medical condition: Solid Neoplasms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004558-30 | Sponsor Protocol Number: BIOP-US | Start Date*: 2019-05-16 | |||||||||||
Sponsor Name:Fundación Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz | |||||||||||||
Full Title: Synovial ultrasound as primary outcome in a 3-arm, randomized, open-label, parallel active controlled, multicenter international study comparing baricitinib, alone and combined with MTX versus TNF-... | |||||||||||||
Medical condition: rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PT (Completed) DK (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000977-62 | Sponsor Protocol Number: 012418QM | Start Date*: 2018-09-28 | |||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||
Full Title: BARBICAN: A randomised, open-label Phase II study to determine the contribution of ipatasertib to neoadjuvant chemotherapy plus atezolizumab in women with triple-negative breast cancer | |||||||||||||
Medical condition: Triple negative breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001599-40 | Sponsor Protocol Number: 23032013 | Start Date*: 2014-01-03 | ||||||||||||||||
Sponsor Name:Charité - Universitätsmedizin Berlin | ||||||||||||||||||
Full Title: Evaluation of the safety, tolerability, efficacy and immunological responses of the interleukin-2 analogue Aldesleukin (Proleukin®) in the treatment of systemic lupus erythematosus as prototypic au... | ||||||||||||||||||
Medical condition: Patients with systemic lupus erythematosus (SLE) and increased disease activity refractory to standard therapies. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003714-14 | Sponsor Protocol Number: 4213000 | Start Date*: 2020-06-30 | |||||||||||
Sponsor Name:TheraOp gGmbH | |||||||||||||
Full Title: Modulation of the FOLFIRI-based standard 1st-line therapy with cetuximab, controlled by monitoring the RAS mutation load by liquid biopsy in RAS-mutated mCRC patients | |||||||||||||
Medical condition: Histologically confirmed, UICC stage IV adenocarcinoma of the left-sided colon or rectum with metastases (metastatic colorectal cancer), primarily non-resectable or surgery refused by the patient, ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001203-79 | Sponsor Protocol Number: IM011021 | Start Date*: 2017-12-04 | |||||||||||
Sponsor Name:Bristol-Myers Squibb international Corporation | |||||||||||||
Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Efficacy and Safety of BMS-986165 in Subjects with Systemic Lupus Erythematosus | |||||||||||||
Medical condition: Systemic Lupus Erythematosus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) DE (Completed) ES (Ongoing) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001132-22 | Sponsor Protocol Number: BGB-A317-NSCL-001 | Start Date*: 2019-05-20 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Celgene Corporation | ||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 3, Randomized, Blinded, Placebo-controlled Study of Tislelizumab (BGB-A317) Plus Chemoradiotherapy Followed by Tislelizumab Monotherapy in Newly Diagnosed, Stage III Subjects with Locally A... | ||||||||||||||||||||||||||||||||||||||
Medical condition: non-small cell lung cancer (NSCLC) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: PT (Completed) ES (Prematurely Ended) FI (Prematurely Ended) PL (Completed) HU (Completed) GB (Completed) IT (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-023584-17 | Sponsor Protocol Number: RAS-AZIC | Start Date*: 2012-08-31 | |||||||||||
Sponsor Name:Universität Leipzig | |||||||||||||
Full Title: Response-Adapted Sequential Azacitidine And Chemotherapy in Patients > 60 Years Old With Newly Diagnosed AML Eligible for Chemotherapy and allogeneic hematopoietic cell transplantation: A Multicent... | |||||||||||||
Medical condition: acute myeloid leukeamia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001443-49 | Sponsor Protocol Number: MK0524A-158 | Start Date*: 2012-11-20 | |||||||||||||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||||||||||||
Full Title: A Single Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ER Niacin/Laropiprant in Adolescents with Heterozygous Familial Hypercholesterolemia | |||||||||||||||||||||||
Medical condition: Heterozygous Familial Hypercholesterolaemia | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) Outside EU/EEA | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004114-35 | Sponsor Protocol Number: ETOP17-20 | Start Date*: 2022-02-21 | ||||||||||||||||
Sponsor Name:European Thoracic Oncology Platform (ETOP) | ||||||||||||||||||
Full Title: A multicentre single-arm phase II trial assessing the safety and efficacy of first-line osimertinib and locally ablative radiotherapy in patients with synchronous oligo-metastatic EGFR-mutant non-s... | ||||||||||||||||||
Medical condition: Treatment naïve patients with synchronous, oligo-metastatic (primary tumour and maximum 5 metastases) EGFR-mutant (exon 19 deletion or exon 21 L858R) NSCLC with or without T790M resistance mutation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) IT (Prematurely Ended) NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003974-29 | Sponsor Protocol Number: D6186C00001 | Start Date*: 2019-08-15 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Biomarker-Directed Phase 2 Platform Study in Patients with Advanced Non-Small Cell Lung Cancer whose Disease has Progressed on First-Line Osimertinib Therapy | |||||||||||||
Medical condition: Advanced Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) NO (Trial now transitioned) DK (Completed) ES (Ongoing) NL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002790-55 | Sponsor Protocol Number: 116389 | Start Date*: 2013-04-08 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A double blind, randomized, placebo controlled phase II study to assess the efficacy of recPRAME +AS15 Antigen-Specific Cancer Immunotherapeutic as adjuvant therapy in patients with resected PRAME-... | |||||||||||||
Medical condition: Non-Small Cell Lung Cancer (Stage IA-T1b, IB, II or IIIA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003148-11 | Sponsor Protocol Number: MoA-Ustekinumab | Start Date*: 2015-01-29 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Academic Medical Center | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Mechanism of action study of Ustekinumab treatment in psoriatic arthritis: Impact on cellular and molecular pathways of synovial inflammation and tissue remodeling | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: psoriatic arthritis | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003167-58 | Sponsor Protocol Number: WO29074 | Start Date*: 2014-04-14 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE II, RANDOMIZED STUDY OF ATEZOLIZUMAB (ANTI−PD-L1 ANTIBODY) ADMINISTERED AS MONOTHERAPY OR IN COMBINATION WITH BEVACIZUMAB VERSUS SUNITINIB IN PATIENTS WITH UNTREATED ADVANCED RENAL CELL CAR... | |||||||||||||
Medical condition: ADVANCED RENAL CELL CARCINOMA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) IT (Completed) GB (Completed) ES (Completed) FR (Completed) RO (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001136-28 | Sponsor Protocol Number: OSE-279-C101 | Start Date*: 2022-11-08 | ||||||||||||||||||||||||||
Sponsor Name:OSE Immunotherapeutics | ||||||||||||||||||||||||||||
Full Title: A multicenter, phase 1/2, dose-finding and dose expansion study of OSE-279, a PD-1 blocking monoclonal antibody, in subjects with advanced solid tumors or lymphomas | ||||||||||||||||||||||||||||
Medical condition: Advanced solid tumors and lymphomas | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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