- Trials with a EudraCT protocol (1,699)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,699 result(s) found for: Chemistry.
Displaying page 71 of 85.
| EudraCT Number: 2017-003668-11 | Sponsor Protocol Number: E7080-G000-604 | Start Date*: 2018-07-30 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Eisai Ltd. | ||||||||||||||||||||||||||||||||||||||
| Full Title: An open-label, multi-center, roll-over study to assess long term safety of lenvatinib monotherapy or lenvatinib combination regimen or comparator treatment arm to cancer patients in Eisai sponsored... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: solid tumors or lymphomas, as defined in parent protocol | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) NL (Completed) ES (Prematurely Ended) BE (Completed) IT (Completed) RO (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-004184-12 | Sponsor Protocol Number: DTX401-CL301 | Start Date*: 2022-08-22 | |||||||||||
| Sponsor Name:Ultragenyx Pharmaceutical Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled Study of Adeno-associated Virus Serotype 8-mediated Gene Transfer of Glucose-6-phosphatase in Patients With Glycogen Storage Disease Type Ia.... | |||||||||||||
| Medical condition: Glycogen Storage Disease Type Ia (GSDIa). | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) ES (Trial now transitioned) IT (Trial now transitioned) DK (Trial now transitioned) PT (Completed) DE (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004104-34 | Sponsor Protocol Number: SNDX-5613-0700 | Start Date*: 2022-04-20 | |||||||||||
| Sponsor Name:Syndax Pharmaceuticals, Inc | |||||||||||||
| Full Title: A Phase 1/2, Open-label, Dose-Escalation and Dose-Expansion Cohort Study of SNDX-5613 in Patients with Relapsed/Refractory Leukemias, Including Those Harboring an MLL/KMT2A Gene Rearrangement or Nu... | |||||||||||||
| Medical condition: Relapsed or Refractory Acute Leukemias | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Trial now transitioned) FR (Trial now transitioned) ES (Ongoing) LT (Trial now transitioned) DE (Temporarily Halted) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-011181-28 | Sponsor Protocol Number: SP954 | Start Date*: 2009-11-02 | |||||||||||
| Sponsor Name:Schwartz Biosciences, INC - UCB Group | |||||||||||||
| Full Title: An open-label, multicenter, multinational study of lacosamide as first add-on anti epileptic drug (AED) treatment in subjects with partial onset seizures. ESTUDIO ABIERTO, MULTICÉNTRICO Y MULTINACI... | |||||||||||||
| Medical condition: Epilepsy / Epilepsia | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) AT (Completed) FI (Completed) IT (Completed) PL (Completed) NL (Prematurely Ended) BG (Completed) FR (Completed) GR (Completed) HU (Completed) PT (Prematurely Ended) DE (Completed) CZ (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-004972-20 | Sponsor Protocol Number: MS200527ˍ0080 | Start Date*: 2020-11-05 | ||||||||||||||||
| Sponsor Name:Merck Healthcare KGaA | ||||||||||||||||||
| Full Title: A Phase III, Multicenter, Randomized, Parallel Group, Double Blind, Double Dummy, Active Controlled Study of Evobrutinib Compared with Teriflunomide, in Participants with Relapsing Multiple Scleros... | ||||||||||||||||||
| Medical condition: Relapsing Multiple Sclerosis | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Prematurely Ended) GB (GB - no longer in EU/EEA) AT (Prematurely Ended) HU (Prematurely Ended) BE (Completed) CZ (Completed) BG (Completed) ES (Completed) FI (Prematurely Ended) HR (Completed) IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-004980-36 | Sponsor Protocol Number: MS200527-0082 | Start Date*: 2020-09-21 | ||||||||||||||||
| Sponsor Name:Merck Healthcare KGaA | ||||||||||||||||||
| Full Title: A Phase III, Multicenter, Randomized, Parallel Group, Double Blind, Double Dummy, Active Controlled Study of Evobrutinib Compared with Teriflunomide, in Participants with Relapsing Multiple Scleros... | ||||||||||||||||||
| Medical condition: Relapsing Multiple Sclerosis | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: PT (Prematurely Ended) LT (Completed) SK (Completed) LV (Completed) GR (Completed) BG (Completed) PL (Prematurely Ended) NO (Prematurely Ended) ES (Completed) DE (Prematurely Ended) SI (Completed) IT (Prematurely Ended) RO (Completed) CZ (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2022-002441-18 | Sponsor Protocol Number: D6582C00001 | Start Date*: 2022-10-27 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Phase IIa Randomised, Double-Blind, Placebo Controlled, Parallel Arm, Multi-Centre Study to Evaluate the Efficacy and Safety of AZD4831, for 12-24 Weeks, in Moderate to Severe Chronic Obstructive... | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) ES (Ongoing) NL (Completed) IT (Completed) BG (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005487-22 | Sponsor Protocol Number: A2A-005 | Start Date*: 2022-12-21 | |||||||||||
| Sponsor Name:iTeos Belgium SA | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, Phase 2 study evaluating efficacy and safety of inupadenant in combination with carboplatin and pemetrexed in adults with nonsquamous non-small cell ... | |||||||||||||
| Medical condition: Nonsquamous non-small cell lung cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) BE (Trial now transitioned) ES (Ongoing) PL (Completed) DE (Ongoing) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-006173-27 | Sponsor Protocol Number: NV06-0039 | Start Date*: 2007-07-16 | |||||||||||
| Sponsor Name:Marshall Edwards Pty Limited | |||||||||||||
| Full Title: Multi-Center, Randomized, Double-Blind, Phase III Efficacy Study Comparing Phenoxodiol (Oral Dosage Form) in Combination with Carboplatin versus Carboplatin with Placebo in Patients with Platinum-R... | |||||||||||||
| Medical condition: Patients with Platinum-Resistant or Platinum-Refractory, Late-Stage Epithelial Ovarian, Fallopian or Primary Peritoneal Cancer Following at Least Second Line Platinum Therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-024006-35 | Sponsor Protocol Number: C38072/3083 | Start Date*: 2011-05-05 | |||||||||||
| Sponsor Name:Teva Branded Pharmaceutical Products, R&D, Inc. | |||||||||||||
| Full Title: A 12-Month, Double-Blind, Placebo-Controlled, Parallel-Group Study to evaluate the Efficacy and Safety of Reslizumab (3.0 mg/kg) in the reduction of Clinical Asthma Exacerbations in Patients (12-75... | |||||||||||||
| Medical condition: Treatment for patients with eosinophilic asthma | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) DE (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003897-41 | Sponsor Protocol Number: D1699C00001 | Start Date*: 2017-01-19 |
| Sponsor Name:AstraZeneca AB | ||
| Full Title: Study to Evaluate the Effect of Dapagliflozin on the Incidence of Worsening Heart Failure or Cardiovascular Death in Patients with Chronic Heart Failure with Reduced Ejection Fraction | ||
| Medical condition: Chronic Heart Failure (HF) with Reduced Ejection Fraction | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) CZ (Completed) DE (Completed) DK (Completed) BG (Completed) SK (Completed) PL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-002885-38 | Sponsor Protocol Number: HGT-HIT-094 | Start Date*: 2013-10-22 | |||||||||||
| Sponsor Name:Shire HGT Inc | |||||||||||||
| Full Title: A Controlled,Randomized,Two-arm,Open-label,Assessor-blinded,Multicenter Study of Intrathecal Idursulfase-IT Administered in Conjunction with Elaprase® in Pediatric Patients with Hunter Syndrome and... | |||||||||||||
| Medical condition: Long-term treatment of Hunter syndrome and cognitive impairment | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004732-19 | Sponsor Protocol Number: 6043-PG-PSC-206 | Start Date*: 2015-07-20 | |||||||||||||||||||||
| Sponsor Name:LETI Pharma GmbH | |||||||||||||||||||||||
| Full Title: A Randomised, Double-Blind, Parallel Group, Multicentre Study to Assess the Efficacy and Safety of Four Concentrations of Depigoid® Phleum versus Placebo in Patients with Allergic Rhinitis and/or R... | |||||||||||||||||||||||
| Medical condition: Allergic Rhinitis and / or Rhinoconjunctivitis with or without Intermittent Asthma | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) PL (Completed) ES (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2010-022284-35 | Sponsor Protocol Number: R00002 CR 301 (ORF) | Start Date*: 2011-03-08 | |||||||||||
| Sponsor Name:ORFAGEN | |||||||||||||
| Full Title: CLINICAL EFFICACY AND SAFETY OF TAZAROTENE CREAM 0.05% IN THE INITIAL AND MAINTENANCE THERAPIES OF LAMELLAR ICHTHYOSIS (LI) | |||||||||||||
| Medical condition: Lamellar Ichthyosis (LI) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) SE (Completed) DE (Completed) FR (Ongoing) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-006556-21 | Sponsor Protocol Number: CRAD001J2301 | Start Date*: 2009-09-26 | |||||||||||
| Sponsor Name:Novartis Pharma Service AG | |||||||||||||
| Full Title: Randomized Phase III, Double-Blind, Placebo-Controlled Multicenter Trial of Everolimus in Combination with Trastuzumab and Paclitaxel, as First Line Therapy in Women with HER2 Positive Locally Adva... | |||||||||||||
| Medical condition: HER2+ locally advanced or metastatic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) FR (Completed) IT (Completed) IE (Completed) BE (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002570-23 | Sponsor Protocol Number: CAUY922A2205 | Start Date*: 2011-12-22 | ||||||||||||||||
| Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
| Full Title: An open-label, single-arm, multi-center phase II study to evaluate the efficacy and safety of AUY922 in combination with trastuzumab standard therapy as second-line treatment in patients with HER2-... | ||||||||||||||||||
| Medical condition: Patients with documented advanced HER2 positive gastric cancer progressing after clinical benefit to 1st line treatment with trastuzumab containing treatment. Clinical benefit is defined as overall... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Prematurely Ended) DE (Completed) ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-004944-31 | Sponsor Protocol Number: EVE-AT-0412 | Start Date*: 2014-06-27 | |||||||||||
| Sponsor Name:EVER Neuro Pharma GmbH | |||||||||||||
| Full Title: Comparison of Cerebrolysin and donepezil: A randomized, double-blind, controlled trial on efficacy and safety in patients with mild to moderate Alzheimer’s disease | |||||||||||||
| Medical condition: Mild to moderate dementia of Alzheimer type (DAT) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) ES (Completed) PL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003241-89 | Sponsor Protocol Number: LCP-Tacro 3002 | Start Date*: 2010-11-05 | |||||||||||
| Sponsor Name:LifeCycle Pharma A/S | |||||||||||||
| Full Title: A Phase 3, Double-Blind, Double-Dummy, Multi-Center, Prospective, Randomized Study of the Efficacy and Safety of LCP-Tacro™ Tablets, Once Daily, Compared to Prograf® Capsules, Twice Daily, in Combi... | |||||||||||||
| Medical condition: Prevention of Acute Allograft Rejection in De Novo Adult Kidney Transplant Recipients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) SE (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-001012-35 | Sponsor Protocol Number: G200802 | Start Date*: 2015-10-06 | ||||||||||||||||||||||||||
| Sponsor Name:GTx, Inc. | ||||||||||||||||||||||||||||
| Full Title: A Phase 2 Open Label, Multi-Center, Multinational, Randomized, Parallel Design Study Investigating The Efficacy and Safety Of GTx-024 On Metastatic or Locally Advanced ER+/AR+ Breast Cancer (BC) in... | ||||||||||||||||||||||||||||
| Medical condition: Estrogen Receptor Positive and Androgen Receptor Positive Breast Cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: BG (Prematurely Ended) HU (Prematurely Ended) LT (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2021-001205-73 | Sponsor Protocol Number: IMP4297-202 | Start Date*: 2021-08-24 | ||||||||||||||||
| Sponsor Name:IMPACT Therapeutics, Inc. | ||||||||||||||||||
| Full Title: A Randomized, Double-Blinded, Placebo-Controlled, Multicenter, Phase II Study to Evaluate Senaparib Maintenance in mCRPC Patients with Homologous Recombination Repair Gene Alterations after Docetax... | ||||||||||||||||||
| Medical condition: metastatic castration-resistant prostate cancer (mCRPC) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: BE (Completed) FR (Completed) ES (Ongoing) IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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