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A Phase 2 Study of Tarlatamab in Patients With Small Cell Lung Cancer (SCLC)

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NCT05060016 · readout in 497 d

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

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
222actual
Sites
80
Countries
Austria, Belgium, Denmark +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
Start2021-12-01actualWhen the study began enrolling
Primary completion2027-12-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-12-30estimatedThe whole study's end, after follow-up
First posted2021-09-28actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Relapsed/Refractory Small Cell Lung Cancer

Intervention

  • Drug: Tarlatamab

Primary outcomes

what the primary-completion date above is the date OF
Part 1 Only: Objective Response (OR) per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 by Investigator
measured Up to a maximum of 61 months
Part 1 and Part 3 Only: Number of Participants who Experience One or More Treatment-emergent Adverse Events
measured Up to a maximum of 61 months
Part 1 Only: Serum Concentrations of Tarlatamab
measured Up to a maximum of 24 months
Part 1 and Part 2 Only: Objective Response (OR) per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 by Blinded Independent Central Review (BICR)
measured Up to a maximum of 61 months

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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