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A Study to Investigate the Safety, Tolerability, and PK of AB102 in Healthy Participants

← catalyst calendar

NCT07662057 · readout ≤ 133 d

Sponsored by Arcus Biosciences, Inc. (industry) · RCUS — their whole pipeline →.

Phase
Phase 1
Status
Not yet recruiting
Study type
Interventional
Design
Randomized · Double · Basic science
Enrollment
130estimated

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
StartJul 2026estimatedWhen the study began enrolling
Primary completionDec 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2026estimatedThe whole study's end, after follow-up
First posted2026-06-23actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-25actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Volunteers

Interventions

  • Drug: AB102
  • Other: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Number of participants experiencing Adverse Events (AEs)
measured Up to 49 days
Maximum observed plasma concentration (Cmax) for SAD and MAD Parts
measured Up to 28 days
Time to attain maximum observed plasma concentration (tmax) for SAD and MAD Parts
measured Up to 28 days
Terminal elimination half-life (t1/2) for SAD Part
measured Up to 28 days
Area under the plasma concentration-time curve from time 0 to last sample (AUClast) for SAD and MAD Parts
measured Up to 28 days
Area under the plasma concentration-time curve from time 0 to 24 hours (AUC0-24h) for SAD Part
measured Up to 28 days
Area under the plasma concentration-time curve from time 0 to infinity (AUCinf) for SAD Part
measured Up to 28 days
Area under the plasma concentration-time curve over a dosing interval (AUC0-tau) for MAD Part
measured Up to 28 days
Accumulation ratio (Racc(Cmax))for MAD Part
measured Up to 28 days
Accumulation ratio(Racc(AUCtau)) for MAD Part
measured Up to 28 days

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