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A Study to Compare the Bioavailability of Intravenously Infused Risankizumab Manufactured by Two Different Processes in Healthy Adults

Phase 1
Completed
Conditions
Healthy Volunteers
Interventions
Registration Number
NCT06054425
Lead Sponsor
AbbVie
Brief Summary

The objective of this study is to assess the bioavailability of risankizumab liquid vial manufactured with the new process (CMC3) relative to the current process (CMC2).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
48
Inclusion Criteria
  • Body Mass Index (BMI) >= 18.0 to <= 32.0 kg/m2 after rounding to the tenths decimal at the time of screening and upon initial confinement.
  • A condition of general good health, based upon the results of a medical history, physical examination, vital signs, laboratory profile and a 12-lead electrocardiogram (ECG).
  • Body weight less than 100.00 kg at Screening and upon initial confinement.
Exclusion Criteria
  • History of any clinically significant illness/infection/major febrile illness, hospitalization, or any surgical procedure within 30 days prior to the first dose of study drug.
  • Previous exposure to any anti-interleukin (IL)-12/23 or anti-IL-23 treatment for at least one year prior to Screening.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Arm 1RisankizumabParticipants will receive risankizumab manufactured with using the current process (CMC2).
Arm 2RisankizumabParticipants will receive risankizumab manufactured with using the new process (CMC3).
Primary Outcome Measures
NameTimeMethod
AUC from Time 0 to Infinity (AUC0-inf)Up to Day 131

AUC0-inf will be assessed.

Terminal Phase Elimination Half-life (t1/2)Up to Day 131

Terminal phase elimination half-life (t1/2) will be assessed.

Maximum Observed Serum Concentration (Cmax)Up to Day 131

Cmax will be assessed.

Apparent Terminal Phase Elimination Rate Constant (β)Up to Day 131

Apparent terminal phase elimination rate constant (β) will be assessed.

Time to Cmax (Tmax)Up to Day 131

Tmax will be assessed.

Area Under the Concentration-time Curve (AUC) from Time 0 to Time of the Last Measurable Concentration (AUC0-t)Up to Day 131

AUC0-t will be assessed.

Number of Participants with Adverse Events (AEs)Baseline to Day 141

An adverse event (AE) is defined as any untoward medical occurrence in a patient or clinical investigation participant administered a pharmaceutical product which does not necessarily have a causal relationship with this treatment.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (3)

Anaheim Clinical Trials LLC /ID# 260740

🇺🇸

Anaheim, California, United States

Clinical Pharmacology of Miami /ID# 260800

🇺🇸

Miami, Florida, United States

Acpru /Id# 260864

🇺🇸

Grayslake, Illinois, United States

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