Novartis Investigative site
Aurora, Colorado 80010
We've found
10 trials
at this facility
Neoplasms, Breast Clinical Trial
Updated: 4/4/2016
EAP (Expanded Access Protocol) Of Lapatinib Combined With Capecitabine In Metastatic Breast Cancer
Status: Enrolling,
Phase
IV
Updated: 4/4/2016
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Multiple Sclerosis Clinical Trial
Updated: 12/31/1969
Safety Study in Patients With Multiple Sclerosis Treated Fingolimod or Other Approved Disease-modifying Therapies
Status: Enrolling,
Phase
Updated: 12/31/1969
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Idiopathic Pulmonary Fibrosis Clinical Trial
Updated: 12/31/1969
Study of Pharmacodynamics, Pharmacokinetics, Safety and Tolerability of VAY736 in Patients With Idiopathic Pulmonary Fibrosis
Status: Enrolling,
Phase
II
Updated: 12/31/1969
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Acute Demylelinating Optic Neuritis Clinical Trial
Updated: 1/17/2014
Fingolimod (FTY720) in Acute Demyelinating Optic Neuritis (ADON)
Status: Enrolling,
Phase
II
Updated: 1/17/2014
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Retinopathy of Prematurity Clinical Trial
Updated: 12/31/1969
Rainbow Extension Study
Status: Enrolling,
Phase
III
Updated: 12/31/1969
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Pediatric Heart Failure Clinical Trial
Updated: 12/31/1969
Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of LCZ696 Followed by a 52-week Study of LCZ696 Compared With Enalapril in Pediatric Patients With Heart Failure
Status: Enrolling,
Phase
II, III
Updated: 12/31/1969
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Solid Tumours Clinical Trial
Updated: 12/31/1969
Pazopanib Paediatric Phase II Trial Children's Oncology Group (COG) in Solid Tumors
Status: Enrolling,
Phase
II
Updated: 12/31/1969
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Relapsing Multiple Scelrosis Clinical Trial
Updated: 12/31/1969
Efficacy and Safety of Ofatumumab Compared to Teriflunomide in Patients With Relapsing Multiple Sclerosis.
Status: Enrolling,
Phase
III
Updated: 12/31/1969
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Heart Failure With Preserved Ejection Fraction Clinical Trial
Updated: 12/31/1969
A Randomized, Double-blind Controlled Study Comparing LCZ696 to Medical Therapy for Comorbidities in HFpEF Patients
Status: Enrolling,
Phase
III
Updated: 12/31/1969
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Multiple Sclerosis Clinical Trial
Updated: 12/31/1969
A 12 Week Randomized Open Label Parallel Group Multicenter Study to Evaluate Bioequivalence of 20 mg Subcutaneous Ofatumumab Injected by Pre-filled Syringe or Autoinjector in Adult RMS Patients
Status: Enrolling,
Phase
II
Updated: 12/31/1969
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