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ABBV-1451

Phase 1

Healthy Volunteer | Small molecule | Other |AbbVie Inc.|Last Updated: May 28, 2026

Success Probability
Approval Probability 71%
TA Base Rate26%
Adjusted LOA41%
ML RiskLOW_RISK
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Market & Valuation
rNPV $3.2B
Market Size $9.4B
Revenue Basis $1.6B
Competitors 6
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Trial Design
RandomizedDouble-BlindCONTROLLED
Total Trials1
Total Enrollment90
FDA Designations
No designations recorded
Clinical Trials (1)
NCT IDTitlePhaseStatusEnrollmentVelocityDesignStartCompletionLast UpdatedSitesCountries
NCT07570147A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Single Ascending Doses of ABBV-1451 Infusions and Injections in Healthy Adult ParticipantsPHASE1 RECRUITING 90May 1, 2026Apr 1, 2027May 28, 20261 United States
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Study Endpoints
Primary Endpoints
Number of Participants with Adverse Events (AEs)
Up to Approximately Day 211

An AE is defined as any untoward medical occurrence in a patient or clinical investigation in which a participant is administered a pharmaceutical product which does not necessarily have a causal relationship with this treatment. The investigator assesses the relationship of each event to the use of study.

Maximum Observed Plasma Concentration (Cmax) of ABBV-1451
Up to Approximately Day 211

Cmax of ABBV-1451.

Time to Cmax (Tmax) of ABBV-1451
Up to Approximately Day 211

Tmax of ABBV-1451.

Terminal Phase Elimination Rate Constant (β) of ABBV-1451
Up to Approximately Day 211

β of ABBV-1451.

Terminal Phase Elimination Half-Life (t1/2) of ABBV-1451
Up to Approximately Day 211

t1/2 of ABBV-1451.

Area Under the Plasma Concentration-Time Curve From Time 0 to Time of Last Measurable Concentration (AUCt) of ABBV-1451
Up to Approximately Day 211

AUCt of ABBV-1451.

Area Under the Plasma Concentration-Time Curve From Time 0 to Infinite Time (AUCinf) of ABBV-1451
Up to Approximately Day 211

AUCinf of ABBV-1451.

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Study Design & Arms
AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeBASIC_SCIENCE
Treatment Arms
ArmTypeDescription
Part 1: Group 1EXPERIMENTALParticipants will receive either single ascending doses of ABBV-1451 until they reach Dose A or placebo.
Part 1: Group 2EXPERIMENTALParticipants will receive either single ascending doses of ABBV-1451 until they reach Dose B or placebo.
Part 1: Group 3EXPERIMENTALParticipants will receive either single ascending doses of ABBV-1451 until they reach Dose C or placebo.
Part 1: Group 4EXPERIMENTALParticipants will receive either single ascending doses of ABBV-1451 until they reach Dose A or placebo.
Part 1: Group 5EXPERIMENTALParticipants will receive either single ascending doses of ABBV-1451 until they reach Dose C or placebo.
Part 1: Group 6EXPERIMENTALParticipants will receive either single ascending doses of ABBV-1451 until they reach Dose TBD or placebo.
Part 2: Group 7EXPERIMENTALJapanese participants will receive a single dose of ABBV-1451 Dose C or placebo.
Part 2: Group 8EXPERIMENTALHan Chinese participants will receive a single dose of ABBV-1451 Dose C or placebo.
Interventions
NameTypeDescription
ABBV-1451DRUGInjection
PlaceboOTHERInjection
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Eligibility Criteria
Age Range18 Years — 60 Years
SexALL
Healthy VolunteersYes
Study Sites1

Inclusion Criteria: * A condition of general good health, based upon the results of a medical history, physical examination, vital signs, laboratory profile and a 12-lead ECG. * Applies to Part 2 only: * For Japanese participants: \-- Participant must be first or second-generation Japanese of fu...

Countries:United States
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Recent Changes (Last 90 Days)
LOWMay 29, 2026NCT07570147Status: NOT_YET_RECRUITING → RECRUITING
LOWMay 29, 2026NCT07570147Status: NOT_YET_RECRUITING → RECRUITING
LOWMay 29, 2026NCT07570147Status: NOT_YET_RECRUITING → RECRUITING
LOWMay 24, 2026NCT07570147studyFirstPostDate: changed
LOWMay 21, 2026NCT07570147NEW_TRIAL: changed
LOWMay 21, 2026NCT07570147NEW_TRIAL: changed