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A Study of Subcutaneous Trastuzumab Deruxtecan in Participants With Metastatic Solid Tumors

← catalyst calendar

NCT07015697 · readout in 865 d

Sponsored by Daiichi Sankyo (industry) · 4568.T — their whole pipeline →. With AstraZeneca.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
76estimated
Sites
31
Countries
Brazil, France, Japan +4

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
Start2025-07-17actualWhen the study began enrolling
Primary completion2028-12-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-12-31estimatedThe whole study's end, after follow-up
First posted2025-06-11actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-09actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Recurrent or Metastatic Solid Tumors

Intervention

  • Drug: Trastuzumab Deruxtecan — also filed as T-DXd, ENHERTU®

Primary outcomes

what the primary-completion date above is the date OF
Number of Participants Experiencing a Treatment Emergent Adverse Event (TEAE)
measured From the start of trial intervention to 21 days after the last dose, up to approximately 9 months
Area Under Curve (AUC)
measured From the start of trial intervention to last dose, up to approximately 9 months
Number of Participants with Dose limiting toxicities (DLT) During the Dose-Escalation Phase
measured From the start of trial intervention to 21 days after the last dose, up to approximately 9 months

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