30 closest matches · ranked by relevance
Metastatic Breast Cancer
Primary: Response Rate (RR) — 4.8; 0 percentage of participants
Advanced, Androgen Receptor Positive Triple Negative Breast Cancer
Primary: Percentage of Participants With Clinical Benefit at Week 16: Evaluable Population — 33.3 Percentage of participants
Invasive Breast Carcinoma · Stage I Breast Cancer AJCC v7 · Stage IA Breast Cancer AJCC v7
Primary: RCB Status — 4; 6; 8; 6 Participants
Androgen Receptor Positive · Estrogen Receptor Negative · HER2/Neu Negative
Primary: Response Rate (Complete Response or Partial Response) — 1; 1; 2; 12 Participants
Triple Negative Breast Cancer
Primary: 3 Months Progression Free Survival. Probability That the Cancer Has Not Progressed at 3 Months Calculated With Kaplan Meier. — 15.8 perceent probability at 3 months
Prostate Cancer
Primary: Change From Baseline in Functional Assessment of Cancer Therapy - Prostate (FACT-P) Total Score at 12 Months — -8.04; -6.60; -9.42 Units on a scale
Breast Cancer · Triple Negative Breast Cancer · Stage IV Breast Cancer
Primary: Objective Response Rate — 28; 38 percentage of patients
Breast Cancer
Primary: Clinical Benefit Rate of the Combination of Enzalutamide/ Fulvestrant — 7 Participants
Metastatic Breast Cancer
Primary: Number of Participants With and Without Progression Free Survival (PFS) Events — 92; 30 Participants
Breast Cancer
Primary: Median Progression Free Survival (PFS) — 7.2 months
Breast Cancer
Primary: Objective Response Rate — 0.09 proportion of participants
ER+ and AR+ Breast Cancer
Primary: Clinical Benefit Rate, in Centrally Confirmed Androgen Receptor (AR)+ Subjects — 16; 15 participants
Castration-resistant Prostate Cancer · Metastatic Prostate Cancer · Prostate Cancer
Primary: Prostate Specific Antigen (PSA) Response to Bipolar Androgen Therapy + Nivolumab — 18 Participants
Estrogen Receptor Negative · HER2/Neu Negative · Invasive Breast Carcinoma
Primary: Objective Response Rate (ORR), Defined as the Proportion of Patients Who Have Had a Partial Response (PR) or Complete Response (CR) (RECIST 1.1 Based) Within the First 6…
Advanced Epithelial Ovarian · Recurrent Epithelial Ovarian · Fallopian Tube
Primary: Overall Response Rate — 1.7 percentage of participants with response
Breast Cancer
Primary: Clinical Benefit Rate — 0.12 proportion of participants
HER2 Amplified · Advanced Breast Cancer · Human Epidermal Growth Factor Receptor 2 (HER2)
Primary: Clinical Benefit Rate (CBR) — 23.6 percentage of participants
Triple Negative Breast Cancer
Primary: Efficacy (Objective Response Rate) — 3 Participants
Breast Cancer
Primary: Percent Reduction in Ki-67 Expression From Baseline to Day 15 in Tumor Biopsies — 71.4; 72.9 Percent reduction
Advanced Breast Cancer · HER2/Neu Negative · Triple-Negative Breast Cancer
Primary: Objective Response (OR) — 0; 0; 0; 3 Participants
Triple Negative Breast Cancer
Primary: Efficacy (Objective Response Rate) — 1 Participants
Breast Cancer
Primary: Cohort A: Progression-Free Survival (PFS) — 6.1; 7.4 months — p=0.9237
Breast Cancer
Primary: Phase Ib Primary Outcome: Proportion of Patients Who Experienced DLTs Attributable to Palbociclib, Tucatinib, or Both — 100; 65; 100 percentage of participants
Metastatic Breast Cancer
Primary: Number of Participants With Dose Limiting Toxicities (DLT) in the First Cycle for the Determination of the Maximum Tolerated Dose (MTD) — 0; 0; 2 participants
Invasive Breast Carcinoma · Triple-Negative Breast Carcinoma
Primary: RCB Status — 0; 1; 13; 3 participants
Breast Cancer Metastatic
Primary: Progression-free Survival (PFS) — 5 months
Breast Cancer
Primary: Objective Response Rate (ORR) Determined by Clinical Palpation — 58.9; 53.8 percentage of participants
Breast Cancer
Primary: Number of Participants With Serious Adverse Events (SAEs) — 10 Participants
Hormone Receptor Positive Malignant Neoplasm of Breast · Human Epidermal Growth Factor 2 Negative Carcinoma of Breast · Estrogen Receptor Positive Breast Cancer
Primary: Progression Free Survival (PFS) Per RECIST 1.1 — 9.13 Months
Advanced Breast Cancer
Primary: Incidence Rate of DLT Within the First Two Cycles of LDE225 (Sonidegib) in Combination With Docetaxel — 0; 0; 0 Participants