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A Study of Dato-DXd in Chinese Patients With Advanced Non-Small Cell Lung Cancer, Triple-negative Breast Cancer and Other Solid Tumors (TROPION-PanTumor02)

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NCT05460273 · results posted

Sponsored by AstraZeneca (industry) · AZN — their whole pipeline →. With Daiichi Sankyo.

Phase
Phase 1/2
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
119actual
Sites
21
Country
China

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
Start2022-07-11actualWhen the study began enrolling
Primary completion2023-11-07actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-06-30estimatedThe whole study's end, after follow-up
First posted2022-07-15actualWhen this record first appeared on the registry
Results posted2025-06-13actualWhen the sponsor posted results to the registry
Record updated2026-07-02actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Carcinoma, Non-Small-Cell Lung
  • Triple Negative Breast Cancer

Intervention

  • Drug: Datopotamab Deruxtecan (Dato-DXd) — also filed as DS-1062a

Primary outcome

what the primary-completion date above is the date OF
Confirmed Objective Response Rate(ORR) Assessed by Independent Central Review(ICR)
measured TNBC cohort: from enrollment to 13 months post last subject dose with a median of 12 months follow up. NSCLC cohort: from enrollment to 20 months post last subject dose with a median of 16.7 months follow up.

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2023-05-29 · 7.4 MB · Prot_000.pdf
Statistical Analysis Planposted 2023-08-30 · 1.2 MB · SAP_001.pdf

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