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Pharmacokinetic Similarity Between ABP 234 and Keytruda® (Pembrolizumab)

← catalyst calendar

NCT06430866 · readout in 116 d

Sponsored by Amgen (industry) · AMGN — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
163actual
Sites
128
Countries
Argentina, Bulgaria, Chile +15

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
Start2024-09-12actualWhen the study began enrolling
Primary completion2026-12-14estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-12-14estimatedThe whole study's end, after follow-up
First posted2024-05-28actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-01actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Early-stage Non-squamous Non-small Cell Lung Cancer (NSCLC)

Interventions

  • Drug: ABP 234
  • Drug: Pembrolizumab

Primary outcomes

what the primary-completion date above is the date OF
Area Under the Serum Concentration-time Curve (AUC) From Time 0 to 21 Days (AUC21d) Following the First Dose
measured 21 days
AUC at Steady State Between Week 16 and Week 19 (AUCtau_ss)
measured Weeks 16-19

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