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RECRUITING Phase 2

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

NCT05489211 · View on ClinicalTrials.gov ↗

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.

Interventions

  • DRUG Carboplatin
  • DRUG Capecitabine
  • DRUG 5-Fluorouracil
  • DRUG Volrustomig
  • DRUG Datopotamab deruxtecan (Dato-DXd)

Study Locations (20)

California

  • Research Site — Los Angeles
  • Research Site — San Diego
  • Research Site — Santa Rosa

Massachusetts

  • Research Site — Boston
  • Research Site — Boston

Ohio

  • Research Site — Cincinnati
  • Research Site — Columbus

Tennessee

  • Research Site — Nashville
  • Research Site — Nashville

Ontario

  • Research Site — Toronto
  • Research Site — Toronto

Indiana

  • Research Site — Muncie

Kansas

  • Research Site — Kansas City

Michigan

  • Research Site — Grand Rapids

Trial Details

FieldValue
Enrollment Target 454 participants
Start Date 2022-09-06
Est. Completion 2027-10-01
Phase Phase 2

Sponsor

AstraZeneca

1,053 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05489211

The ClinicalTrials.gov registry entry for NCT05489211 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 454 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AstraZeneca, which has 1,053 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 7 conditions, with Colorectal Cancer appearing as the primary indexed condition, and to 5 interventions — of which Carboplatin is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05489211 reports 20 study locations spanning 14 distinct geographic areas — top geographies include California, Massachusetts, Ohio. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05489211 about?

NCT05489211 is a clinical study titled "Study of Dato-DXd as Monotherapy and in Combination With Anti-cancer Agents in Patients With Advanced Solid Tumours (TROPION-PanTumor03)". 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.

What is the current status of trial NCT05489211?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 454 participants. The study started on 2022-09-06. Estimated completion is 2027-10-01.

What conditions does trial NCT05489211 study?

This clinical trial studies the following conditions: Colorectal Cancer, Ovarian Cancer, Endometrial Cancer, Gastric Cancer, Metastatic Castration-resistant Prostate Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05489211?

The interventions under investigation include: Carboplatin (DRUG), Capecitabine (DRUG), 5-Fluorouracil (DRUG), Volrustomig (DRUG), Datopotamab deruxtecan (Dato-DXd) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05489211?

This trial is sponsored by AstraZeneca, which has 1,053 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05489211 being conducted?

This trial has 20 study locations across California, Indiana, Kansas, Massachusetts, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial