Study of Dato-DXd as Monotherapy and in Combination With Anti-cancer Agents in Patients With Advanced Solid Tumours (TROPION-PanTumor03)

NCT05489211 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 454

Last updated 2026-03-19

No results posted yet for this study

Summary

TROPION-PanTumor03 will investigate the safety, tolerability, and anti-tumour activity of Datopotamab Deruxtecan (Dato-DXd) as Monotherapy and in Combination with Anticancer Agents in Patients with Advanced/Metastatic Solid Tumours.

Conditions

Interventions

DRUG

Datopotamab deruxtecan (Dato-DXd)

Intravenous (IV) Antibody drug conjugate

DRUG

Capecitabine

Administered orally

DRUG

5-Fluorouracil

Administered as an IV

DRUG

Volrustomig

Administered as an IV

DRUG

Carboplatin

Administered as an IV

DRUG

Bevacizumab

Administered as an IV

DRUG

Rilvegostomig

Administered as an IV

DRUG

Prednisone/ prednisolone

Administered orally

DRUG

Cisplatin

Administered as an IV

Sponsors & Collaborators

Principal Investigators

  • Global Clinical Lead, MD · AstraZeneca

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
130 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-06
Primary Completion
2027-10-01
Completion
2027-10-01
FDA Drug
Yes

Countries

  • United States
  • Canada
  • China
  • France
  • Germany
  • Italy
  • Japan
  • Poland
  • South Korea
  • Spain
  • Switzerland
  • Taiwan
  • Turkey (Türkiye)
  • United Kingdom

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05489211 on ClinicalTrials.gov