EICHORCondition: Adalimumab · Sponsor: Amgen
To determine the pharmacokinetic (PK) comparability of ABP 501 40 mg/0.4 mL (ABP 501-HCF) compared to ABP 501 40 mg/0.8 mL (ABP 501-LCF) following single-dose subcutaneous (SC) injection, as assessed principally by area under the serum concentration-time curve (AUC) from time 0 extrapolated to infinity (AUCinf) and maximum observed serum concentration (Cmax) in healthy adult participants.
This description comes directly from the study's public registry record.
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| WCCT Global, Inc | Cypress, California, United States | — |
| Qps-Mra, Llc | South Miami, Florida, United States | — |
| Pharmaceutical Research Associates, Inc | Salt Lake City, Utah, United States | — |
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Source record: clinicaltrials.gov/study/NCT05909852