4,901 trials
Healthy
Primary: Area Under the Curve of Digoxin From 0 to Last Quantifiable Data Point (AUC 0-tz) — 11.549; 11.981 nanomole hour per liter (nmol·h/L)
Healthy Volunteers
Primary: Pharmacokinetics (PK): Area Under the Concentration-Time Curve From Zero to Infinity [AUC(0-∞)] of LY2835219 and ¹³C₈-LY2835219 — 3730; 15.4 nanogram*h/milliliter…
Healthy Volunteers
Primary: Number of Participants With One or More Drug Related Adverse Events (AEs) or Any Serious AE — 0; 0; 0; 0 Participants
Advanced Cancer · Metastatic Cancer
Primary: Recommended Dose for Phase 2 Studies — 4.0; 6.0 mg/m²/day
Neoplasms
Primary: Number of Participants With Dose Limiting Toxicities (DLTs) in Process for the Determination of the Maximum Tolerated Dose (MTD). — 0; 0; 2 Participants
Type 2 Diabetes Mellitus · Hepatic Impairment
Primary: Area Under the Plasma Concentration-Time Curve From Time 0 to Time of the Last Quantifiable Concentration (AUClast) for Ertugliflozin — 1413; 1618 ng•hr/mL
Healthy
Primary: Pharmacokinetics: Area Under the Concentration Versus Time Curve From Time Zero to Infinity (AUC [0-inf]) for Both Fed and Fasted Periods for Abemaciclib and Major…
Healthy
Primary: Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve From Zero to Infinity (AUC[0-∞]) — 3080; 2880; 3110; 3120 Nanograms*hour/milliliter (ng*hr/mL)
Diabetes Mellitus, Type 1
Primary: Number of Participants With Dose Limiting or Intolerable Treatment Related Adverse Events (AEs) — 0; 0; 0; 0 participants
Healthy
Primary: Mean Time Matched Placebo-Adjusted Changes From Baseline For Fridericia's Corrected QT Interval (ΔΔQTcF) — 1.4; 3.3; 0.2; -2.1 Millisecond (msec)
Healthy Volunteers
Primary: Pharmacokinetics (PK): Maximum Concentration (Cmax) of LY2835219 — 134; 10.5 nanogram per milliliter (ng/ml)
Neoplasm · Neoplasm Metastasis
Primary: Pharmacokinetics (PK): Area Under the Concentration Time Curve From Zero to Infinity (AUC[0-∞]) of Abemaciclib — 2230; 6850 nanogram*hour/milliliter(mL) ng*h/mL
Hepatitis B
Primary: Number of Participants With Any Non-serious Adverse Event (AE); Any Serious AE (SAE); Any AEs Leading to Discontinuation of Study Treatment (AELD) in Part 1 — 4; 3; 2; 3…
Leukemia, Myeloid, Acute
Primary: Number of Participants With Dose Limiting Toxicities (DLT) in Cycle 1 for the Determination of the Maximum Tolerated Dose (MTD) of Volasertib — 0; 0; 1 Participants
Myelodysplastic Syndromes · Leukemia, Myelomonocytic, Chronic
Primary: Number of Participants With Dose Limiting Toxicities (DLTs) in the First Cycle for the Determination of the Maximum Tolerated Dose (MTD) — 2 Participants