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Study of Tarlatamab in Combination With YL201 With or Without Anti-programmed Death Ligand 1 (PD-L1) in Participants With Extensive Stage (ES) Small Cell Lung Cancer (SCLC)

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NCT06898957 · readout in 1,769 d

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

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
29actual
Sites
36
Countries
Canada, China, France +7

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
Start2025-05-16actualWhen the study began enrolling
Primary completion2031-06-23estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2031-06-23estimatedThe whole study's end, after follow-up
First posted2025-03-27actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Small Cell Lung Cancer

Interventions

  • Drug: YL201
  • Drug: Tarlatamab
  • Drug: Durvalumab

Primary outcomes

what the primary-completion date above is the date OF
Number of Participants Experiencing Dose-limiting toxicities (DLTs)
measured Up to Day 21
Number of Participants Experiencing Treatment-emergent Adverse Events (TEAEs)
measured Up to 3.5 Years

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