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Serviço Nacional de Saúde
República Portuguesa

Hospital Beatriz Ângelo

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Ensaios clínicos com recrutamento fechado


  • FIDELIO: A randomized, double-blind, placebo-controlled, parallel-group, multicenter, event-driven Phase III study to investigate the efficacy and safety of finerenone, in addition to standard of care, on the progression of kidney disease in subjects with type 2 diabetes mellitus and the clinical diagnosis of diabetic kidney disease. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2015-000990-11/PT
  • FIGARO: A randomized, double-blind, placebo-controlled, parallel-group, multicenter, event-driven Phase III study to investigate the efficacy and safety of finerenone on the reduction of cardiovascular morbidity and mortality in subjects with type 2 diabetes mellitus and the clinical diagnosis of diabetic kidney disease in addition to standard of care. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2015-000950-39/PT
  • BI 12897: A multi-centre, double-blind, parallel-group, randomised controlled study to investigate efficacy, safety and tolerability of orally administered BI 409306 during a 12-week treatment period compared to donepezil and placebo in patients with cognitive impairment due to Alzheimer's Disease. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2013-005040-28/PT
  • TRIGGER: A 52 week, randomized, double blind, multinational, multicentre, active controlled, 3-arm parallel group trial comparing CHF 5993 200/6/12.5 µg pMDI (fixed combination of extrafine beclometasone dipropionate plus formoterol fumarate plus glycopyrronium bromide) to CHF 1535 200/6 µg pMDI (fixed combination of extrafine beclomethasone dipropionate plus formoterol fumarate) alone or on top of open-label tiotropium 2.5 µg Respimat® in patients with asthma uncontrolled on high doses of inhaled corticosteroids in combination with long-acting ß2-agonists. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2015-000717-40/PT
  • TRIBUTE: A 52-week, Double Blind, Double dummy, Randomized, Multinational, Multicentre, 2-arm Parallel Group, active Controlled Clinical Trial of fixed combination of beclometasone dipropionate plus formoterol fumarate plus Glycopyrronium bromide administered via pMDI (CHF 5993) versus indacaterol/glycopyrronium (Ultibro®) via DPI in patients with Chronic Obstructive Pulmonary Disease. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-001704-22/PT
  • RESPECT ESUS: Randomized, double-blind, Evaluation in secondary Stroke Prevention comparing the Efficacy and safety of the oral Thrombin inhibitor dabigatran etexilate (110 mg or 150 mg, oral b.i.d.) versus acetylsalicylic acid (100 mg oral q.d.) in patients with Embolic Stroke of Undetermined Source. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2013-003444-24/PT
  • GO29294:A phase III, open-label, multicenter, randomized study to investigate the efficacy and safety of MPDL3280A (anti-PD-L1 antibody) compared with chemotherapy in patients with locally advanced or metastatic urothelial bladder cancer after failure with platinum-containing chemotherapy. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-003231-19/PT

  • Danube: A Phase III, Randomized, Open-label, Controlled, Multi Center, Global Study of First-Line MEDI4736 Monotherapy and MEDI4736 in Combination with Tremelimumab Versus Standard of Care Chemotherapy in Patients with Unresectable Stage IV Urothelial Bladder Cancer. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2015-001633-24/GB
  • GO29438: A phase III, open-label, randomized studyof atezolizumab (mpdl3280a, anti−pd-l1 antibody) in combination with carboplatin or cisplatin+pemetrexe compared with carboplatin or cisplatin+pemetrexed in patients who are chemotherapy-naive and have stage iv non-squamous non−small cell lung cancer. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2015-003605-42/PT
  • FB-7: A Phase II Randomized Clinical Trial Evaluating Neoadjuvant Therapy Regimens with Weekly Paclitaxel plus Neratinib or Trastuzumab or Neratinib and Trastuzumab Followed by Doxorubicin and Cyclophosphamide with Postoperative Trastuzumab in Women with Locally Advanced HER2-Positive Breast Cancer. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2013-004391-35/PT

  • GO29505: A phase II randomized, double-blind study of ipatasertib (GDC-0068), an inhibitor to Akt in combination with paclitaxel as neoadjuvant treatment for patients with early stage triple negative breast cancer. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-003029-16/PT

  • SOLAR-1: A phase III randomized double-blind, placebo controlled study of alpelisib in combination with fulvestrant for men and postmenopausal women with hormone receptor positive, HER2-negative advanced breast cancer which progressed on or after aromatase inhibitor treatment. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2015-000340-42/PT
  • 17403: Phase 2/3 study of rogaratinib (pan FGFR inhibitor) vs chemotherapy in patients with locally advanced or metastatic urothelial carcinoma with a high amount of specific cell growth factor receptors 1 and 3 (FGFR1 and 3) in the tumor cells. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2016-004340-11/PT
  • OLYMPIA: A randomised, double-blind, parallel group, placebo-controlled multi-centre Phase III study to assess the efficacy and safety of olaparib versus placebo as adjuvant treatment in patients with germline BRCA1/2 mutations and high risk HER2 negative primary breast cancer who have completed definitive local treatment and neoadjuvant or adjuvant chemotherapy. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2013-003839-30/PT

  • PHERGain: Chemotherapy-free trastuzumab and pertuzumab in HER2-positive breast cancer: FDG-PET response-adapted strategy. The PHERGain study. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2016-002676-27/PT

  • M15-572: A Phase 3, Randomized, Double-Blind, Study Comparing Upadacitinib (ABT-494) to Placebo and to Adalimumab in Subjects with Active Psoriatic Arthritis Who Have a History of Inadequate Response to at Least One Non-Biologic Disease Modifying Anti-Rheumatic Drug (DMARD) – SELECT – PsA 1. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2016-004130-24/PT

  • SCORED: A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Demonstrate the Effects of Sotagliflozin on Cardiovascular and Renal events in Patients with Type 2 Diabetes, Cardiovascular Risk Factors and Moderately Impaired Renal Function. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2017-002644-32/PT
  • GS-US-418-3898: Combined Phase 2b/3, Double-Blind, Randomized, Placebo-Controlled Studies Evaluating the Efficacy and Safety of Filgotinib in the Induction and Maintenance of Remission in Subjects with Moderately to Severely Active Ulcerative Colitis. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2016-001392-78/PT

  • GARDENIA: Phase III, Randomized, Multicenter Double Blind, Double Dummy Study to evaluate the efficacy and safety of Etrolizumab compared with infliximab in patients with moderate to severe active ulcerative colitis who are naive to TNF inhibitors. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2013-004282-14/PTAKB-6548-CI-0016: Phase 3, Randomized, Open-Label, Active-Controlled Study Evaluating the Efficacy and Safety of Oral Vadadustat for the Correction of Anemia in Subjects with Incident Dialysis Dependent Chronic Kidney Disease (DD-CKD). Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2016-000838-21/PT 

  • Vulcano: A phase III, international, multicenter, randomized and openlabel study to evaluate the efficacy on LDLc and blood pressure reduction and safety of Trinomia® versus usual care in patients with high cardiovascular risk without previous cardiovascular event. Mais informações em: https://www.clinicaltrialsregister.eu/ctr-search/trial/2016-004015-13/PT

  • CA2209-9G7: Phase II multi-institutional proof of concept single-arm trial of Nivolumab in the treatment of patients with platinum-recurrent or platinum-refractory metastatic germ cell tumors

  • PLENO: Open-label, Randomized, 2-arm, Active Comparator Study to Evaluate Safety and Tolerability in Portuguese Patients with Relapsing Remitting Multiple Sclerosis (MS) Transitioning from Current Subcutaneous Interferon Therapy to Peginterferon Beta 1a (PLEGRIDY™)

  • MA30143: An Open-Label, single-arm study to evaluate the effectiveness and safety of Ocrelizumab in patients with early stage relapsing remitting multiple sclerosis

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