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A Study Evaluating Bemarituzumab in Solid Tumors With Fibroblast Growth Factor Receptor 2b (FGFR2b) Overexpression

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NCT05325866

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

Phase
Phase 1/2
Status
Terminated
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
260actual
Sites
115
Countries
Argentina, Australia, Austria +23

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

Why the sponsor stopped it

Sponsor Decision

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-09-23actualWhen the study began enrolling
Primary completion2026-01-28actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-01-28actualThe whole study's end, after follow-up
First posted2022-04-13actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Solid Tumors

Intervention

  • Drug: Bemarituzumab — also filed as AMG 552

Primary outcomes

what the primary-completion date above is the date OF
Part 1: Number of Participants Who Experience a Dose Limiting Toxicity (DLT)
measured Day 1 to Day 28
Part 1: Number of Participants Who Experience a Treatment-emergent Adverse Event (TEAE)
measured Day 1 to 28 days after last dose (a maximum of 2 years)
Part 1: Number of Participants Who Experience a Treatment-related Adverse Event
measured Day 1 to 28 days after last dose (a maximum of 2 years)
Part 2: Objective Response (OR) Rate
measured Up to approximately 2 years

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