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topic_facet:"Recruitment Status: Terminated"
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PubPharm (24.589)
81
Endeavor to Stop Nausea/Vomiting Associated With Pregnancy (E-SNAP) : Endeavor to Stop Nausea/Vomiting Associated With Pregnancy (E-SNAP)
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| 2024
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82
STRIDES - a Clinical Research Study of an Investigational New Drug to Treat Spinocerebellar Ataxia : A Double-blind, Randomized, Placebo Controlled, Trial to Assess Safety and Efficacy of SLS-005 (Trehalose Injection, 90.5 mg/mL for Intravenous Infusion) for the Treatment of Adults With Spinocerebellar Ataxia
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| 2024
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83
A Study of Intraperitoneally Administered AVB-001 in Patients With Serous Adenocarcinoma of the Ovary : A Phase 1/2 Open-Label, Multicenter, Dose Escalation and Expansion Study of AVB-001, an Intraperitoneally Administered, Cell-Generated, Human IL-2 Immunotherapy in Patients With Platinum-Resistant, High-Grade, Serous Adenocarcinoma of the Ovary, Primary Peritoneum, or Fallopian Tube
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| 2024
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84
Pediatric Obesity Management Study : Pediatric Obesity Management Pilot Study
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| 2024
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85
IMM60 and Pembrolizumab in Melanoma and NSCLC : IMPORT-201: A Phase 1 First-in-Human Dose Finding/Randomized Phase 2 Study of IMM60 and Pembrolizumab for Advanced Melanoma and Metastatic NSCLC
enthalten in:
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| 2024
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86
A Phase 2 Study of Intravitreal AVD-104 in Diabetic Macular Edema : A Phase 2 Study to Evaluate the Safety and Treatment Effect of Intravitreal AVD-104 in Participants With Diabetic Macular Edema
enthalten in:
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| 2024
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87
Phase II Study of Tetrathiomolybdate (TM) in Patients With Breast Cancer : A Phase II Study of Tetrathiomolybdate (TM) in Patients With Breast Cancer at Moderate to High Risk of Recurrence
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| 2024
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88
Fasting Study of Olanzapine Tablets 20 mg and Zyprexa® Tablets 20 mg : Single-Dose Fasting In Vivo Bioequivalence Study of Olanzapine Tablets (20 mg; Mylan) and Zyprexa® Tablets (20 mg; Eli Lilly) in Healthy Volunteers
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| 2024
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89
Study of the Effect of Clinical Procedures on Drug Delivery of Mylan Fentanyl Transdermal System 25 µg/hr and Duragesic® 25 µg/hr : Investigational Study of the Effect of Clinical Procedures on Drug Delivery of the Fentanyl Transdermal System (25 µg/hr; Mylan) and Duragesic® (25 µg/hr; Janssen) in Healthy Volunteers
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| 2024
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90
WAVECREST Post Market Clinical Follow-Up (PMCF) Study : A Prospective, Multicenter, Non-randomized, Post-market Clinical Follow-up Study to Confirm Safety and Performance of the Coherex WaveCrest® Left Atrial Appendage Occlusion System in Patients With Non-valvular Atrial Fibrillation
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| 2024
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Thema: Recruitment Status: Terminated
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Recruitment Status: Terminated
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Study Type: Interventional
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Phase: Phase 3
3.058
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2.368
Phase: Phase 4
892
Phase: Phase 1/Phase 2
731
Breast Neoplasms
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669
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653
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596
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588
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569
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428
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