ADR: Adverse Drug Reaction
AE: Adverse Event
AUC: Area Under the Curve
CI: Confidence Interval
Cmax: Maximum Plasma Concentration
Cmin: Minimum Plasma Concentration
CONSORT: Consolidated Standards of Reporting Trials
CR: Complete Response
CRO: Contract Research Organization
DoR: Duration of Response
EFS: Event Free Survival
EHR: Electronic Health Record
EMR: Electronic Medical Record
ePRO: Electronic Patient-Reported Outcomes
GCP: Good Clinical Practice
GFR: Glomerular Filtration Rate
GLP: Good Laboratory Practice
GMP: Good Manufacturing Practices
HR: Hazard’s Ratio
ICF: Informed Consent Form
ICH: International Council for Harmonization
ITT: Intent to Treat
K-M: Kaplan Meier (statistics)
OS: Overall Survival
OR: Objective Response
ORR: Objective Response Rate
P: P-value (statistics)
PD: Pharmacodynamics
PFS: Progressive-free Survival
PK: Pharmacokinetics
PI: Principal Investigator
Prn: As Needed
PR: Partial Response
QC: Quality Control
QoL: Quality of Life
RCT: Randomized Clinical Trial
SAE: Serious Adverse Event
SD: Standard Deviation
SEM: Standard Error of the Mean
TTF: Time to Treatment Failure
TTP: Time To Progression
VAS: Visual Analog Scale
