241 studies found for:    Open Studies | UCSD OR UC San Diego OR VA San Diego
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Rank Status Study
1 Recruiting A Study To Evaluate PF-04449913 With Chemotherapy In Patients With Acute Myeloid Leukemia or Myelodysplastic Syndrome
Condition: Acute Myeloid Leukemia
Interventions: Drug: PF-04449913;   Drug: Low dose ARA-C (LDAC);   Drug: Decitabine;   Drug: Daunorubicin;   Drug: Cytarabine
2 Recruiting A Combination Study of PF-04449913 and Azacitidine In 1st Line MDS, AML and CMML Patients
Condition: Myelodysplastic Syndrome
Interventions: Drug: PF-04449913;   Drug: Azacitidine;   Drug: PF-04449913 Placebo
3 Recruiting A Study Of PF-05082566 As A Single Agent And In Combination With Rituximab
Condition: Lymphoma, Non-Hodgkin
Interventions: Drug: PF-05082566;   Drug: rituximab
4 Recruiting Single-Agent Glasdegib In Patients With Myelofibrosis Previously Treated With Ruxolitinib
Condition: Primary Myelofibrosis; Post-polycythemia Vera Myelofibrosis; Post-essential Thrombocythemia Myelofibrosis
Interventions: Drug: Glasdegib (PF-04449913);   Drug: Placebo
5 Recruiting Study For Patients With NSCLC EGFR Mutations (Del 19 or L858R +/- T790M)
Condition: Non-Small Cell Lung Cancer
Intervention: Drug: PF-06747775
6 Recruiting Crizotinib Plus Pembrolizumab In Alk-Positive Advanced Non Small Cell Lung Cancer Patients
Condition: ALK-positive Advanced NSCLC
Interventions: Drug: Crizotinib;   Drug: Pembrolizumab
7 Unknown  24-hr Intraocular Pressure (IOP) Patterns of Glaucoma Patients After Selective Laser Trabeculoplasty (SLT)
Condition: Glaucoma
Intervention: Device: SLT (selective laser trabeculoplasty ) SENSIMED Triggerfish
8 Recruiting A Study of PF-05082566 In Combination With Mogamulizumab In Patients With Advanced Solid Tumors
Condition: Advanced/Metastatic Solid Tumors
Interventions: Drug: PF-05082566;   Drug: KW-0761
9 Recruiting Implementation of Nucleic Acid Amplification Testing Screening to Identify Acute and Early HIV Infection
Condition: Acute HIV Infection
Intervention: Other: Nucleic Acid Amplification Testing
10 Recruiting Reproductive Health Survivorship Care Plan Pilot
Conditions: Breast Cancer;   Hot Flashes;   Vaginal Dryness;   Estrogen Deprivation Symptoms
Intervention: Behavioral: Text message management prompts
11 Recruiting Long-Term Safety Of PF-00547659 In Ulcerative Colitis
Condition: Ulcerative Colitis
Intervention: Drug: PF-00547659
12 Recruiting A Study Of Oral CP-690,550 As A Maintenance Therapy For Ulcerative Colitis
Condition: Ulcerative Colitis
Interventions: Drug: Placebo;   Drug: CP690,550;   Drug: CP-690,550
13 Recruiting Safety and Effectiveness Study of Endovascular Abdominal Aortic Aneurysm Repair Using the Nellix® System
Condition: Abdominal Aortic Aneurysm (AAA)
Intervention: Device: Nellix System
14 Recruiting A Prospective, Single Arm, Multi-Center Clinical Study in Collaboration With the Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS®) to Evaluate the Thoracotomy Implant Technique of the HeartWare HVAD® System in Patients With Advanced Heart Failure
Condition: Left Sided Heart Failure
Intervention: Device: HeartWare HVAD
15 Recruiting Safety Study of Oral MGCD265 Administered Without Interruption to Subjects With Advanced Malignancies
Condition: Advanced Cancer
Intervention: Drug: MGCD265
16 Recruiting Pragmatic Randomized Trial of Proton vs. Photon Therapy for Patients With Non-Metastatic Breast Cancer: A Radiotherapy Comparative Effectiveness (RADCOMP) Consortium Trial
Condition: Breast Cancer
Interventions: Radiation: Photon;   Radiation: Proton
17 Not yet recruiting Substrate Versus Trigger Ablation for Atrial Fibrillation
Condition: Atrial Fibrillation
Interventions: Procedure: FIRM Ablation;   Procedure: Conventional AF ablation with PVI
18 Recruiting The Dynamics of Human Atrial Fibrillation
Conditions: Atrial Fibrillation;   Atrial Tachyarrhythmia
19 Recruiting Treating Prediabetes in the First Trimester
Conditions: Prediabetes;   Gestational Diabetes
Intervention: Other: Treatment of Prediabetes
20 Not yet recruiting Phase 3 Study to Compare Safety and Efficacy of Smoflipid 20% to Intralipid 20% in Hospitalized Neonates and Infants
Condition: Hospitalized Neonates and Infants, Expected to Require Parenteral Nutrition for 28 Days
Interventions: Drug: Smoflipid 20% (investigational lipid for parenteral nutrition);   Drug: Intralipid® 20%

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Indicates status has not been verified in more than two years