Evolocumab Drug Substance A (Test)
DrugEvolocumab drug substance A will be administered SC.
Other names: AMG 145
NCT Number: NCT07545226
The primary objective of this trial is to evaluate the pharmacokinetics (PK) of two evolocumab drug products in healthy participants.
This study is active but is not currently recruiting participants.
Notify Me18 year–60 year
All sexes
Interventional
Phase 1
Anaheim Clinical Trials, Anaheim, California, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
a. Females must not be pregnant or lactating.
Exclusion criteria
Evolocumab drug substance A will be administered SC.
Other names: AMG 145
Evolocumab drug substance B will be administered SC.
Other names: AMG 145
Time frame: Day 1 to Day 64
Time frame: Day 1 to Day 64
Time frame: Day 1 to Day 64
Time frame: Day 1 to Day 64
Time frame: Up to Day 64
Time frame: Day 1 and Day 64
Time frame: Day 1 to Day 64
Time frame: Day 1 to Day 64
Amgen
Industry
An Open-Label, Phase 1, Single Dose, Randomized, Parallel-group Study to Evaluate the Relative Bioavailability of Two Evolocumab (AMG 145) Drug Products
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07075640
Healthy Participants
Madison, Wisconsin, United States
View Trial DetailsNCT07622433
Dyslipidemias, Healthy Participants
Brooklyn, Maryland, United States
View Trial DetailsNCT06517914
Brain Diseases, Brain Diseases, Metabolic
Seongnam, Bundang-gu, South Korea
View Trial DetailsNCT07286682
Healthy Participants
Harrow, United Kingdom
View Trial Details