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A Study of Raludotatug Deruxtecan in Participants With Advanced/Metastatic Solid Tumors (REJOICE-PanTumor01)

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NCT06660654 · readout in 407 d

Sponsored by Daiichi Sankyo (industry) · 4568.T — their whole pipeline →. With Merck Sharp & Dohme LLC.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
200estimated
Sites
48
Countries
Belgium, China, Denmark +6

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
Start2025-01-06actualWhen the study began enrolling
Primary completion2027-09-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-09-30estimatedThe whole study's end, after follow-up
First posted2024-10-28actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Advanced Solid Tumor
  • Metastatic Solid Tumors

Intervention

  • Drug: Raludotatug deruxtecan — also filed as R-DXd

Primary outcomes

what the primary-completion date above is the date OF
Objective Response Rate as Assessed by the Investigator (All Cohorts Except ccRCC)
measured Baseline up to 32 months
Disease Control Rate (DCR) as Assessed by the Investigator (ccRCC Cohort Only)
measured Baseline up to 32 months
Number of Participants Reporting Treatment-emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs), and Adverse Events of Special Interest (AESIs) (All Cohorts)
measured Baseline up to 32 months

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