Clinical Trial Search

Primary: Percentage of Participants With PSA<0.05ng/mL (Radical Prostatectomy) or PSA <Nadir+2ng/mL (Prostate Radiation) — 20 Participants

Primary: Change in Number of Subjects With Adverse Events Will be Collected — 22; 18; 17 Participants

Primary: Change in PET Standard Uptake Value SUV Levels Pre-treatment to Post-treatment. — -56 percentage change from baseline

Primary: Number of Participants With an Immune Response — 2; 4; 4; 3 Participants

Primary: Number of Participants With Serious AEs (SAEs), Adverse Events (AEs) Leading to Discontinuation, and Immune-related AEs - Treated Participants — 3; 2; 9; 2 participants

Primary: Overall Survival — 91.6 weeks

Primary: Proportion Responding to Treatment With of the Combination of Ixabepilone and Mitoxantrone Hydrochloride With Prednisone in Hormone Refractory Prostate Cancer Patients…

Primary: Prostate-specific Antigen (PSA) Response Rate — 28; 30 participants

Primary: Evidence of Metastatic Prostate Cancer — 0; 36; 0; 10 Participants

Primary: Proportion of Patients With PSA Decline by 50% From Baseline — 9; 5 Participants

Primary: Gallium Ga 68-DOTATATE Uptake — 11; 4; 1 Participants

Primary: Cancer Detection Performance of FACBC PET/CT — 17; 22; 4; 14 Participants

Primary: Number of Participants Who Received At Least 1 Infusion of Sipuleucel-T in Men With Metastatic Castrate-resistant Prostate Cancer (CRPC) — 98 participants

Primary: Maximum Tolerated Dosage (MTD) of Cabazitaxel-carboplatin in the Phase I Portion of Study — 25 mg/m^2

Primary: Time to Progression (TTP) — 2.5 months

Primary: Composite Time to Disease Progression (cTTP) for Participants Treated With Cixutumumab — 4.9; 3.2 months

Primary: Overall Time to Disease Progression — 10.9; 9.9 Weeks — p=0.719

Primary: Mean Prostate Specific Antigen (PSA) Level — 0.61; 0.70; 0.54 ng/mL

Primary: Median Relapse-Free Survival Time (Biochemical or Clinical) — 45.3 months

Primary: Number of Participants Who Had a Prostate-specific Antigen (PSA) Response — 52 Participants

Primary: Change in Tissue Testosterone and Dihydrotestosterone — 0.156 pg/mg

Primary: Antigen Spreading (i.e., a Broader Immune Response) With Greater Associated Response Score Compared to Docetaxel Alone After 19 Weeks — 4.31; 5.63; 4.00 Score on a scale

Primary: Phase I: Maximum Tolerated Dose (MTD) of TRC105 Given Every Two Weeks. — 20 mg/kg every 2 weeks

Primary: Progression-free Survival (PFS) — 1 Participants

Primary: Measurement of Sensitivity of DCFBC-PET as Determined by Agreement of PET/CT Detection of Metastatic Prostate Cancer With Conventional Imaging Modality (CIM) — 148; 170…

Primary: Percentage of Participants With PSA50 Response — 2 Participants

Primary: Number of Tumor Lesions Detected by 68Ga-RM2 MRI vs 68Ga-RM2 PET/MRI — 92; 127 number of tumor lesions

Primary: Overall Survival

Primary: Metabolic Syndrome — 0; 0 kilograms

Primary: Clinical Benefit Rate From Cabozantinib (XL184) — 10 Participants