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Active, not recruiting Phase 3 Interventional Results available

Trastuzumab Deruxtecan (T-DXd) Alone or in Sequence With THP, Versus Standard Treatment (ddAC-THP), in HER2-positive Early Breast Cancer

ClinicalTrials.gov ID: NCT05113251

Public ClinicalTrials.gov record NCT05113251. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 28, 2026, 1:05 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3 Open-label Trial of Neoadjuvant Trastuzumab Deruxtecan (T-DXd) Monotherapy or T-DXd Followed by THP Compared to ddAC-THP in Participants With High-risk HER2-positive Early-stage Breast Cancer (DESTINY-Breast11)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will look at the efficacy and safety of trastuzumab deruxtecan (T-DXd) in a neoadjuvant setting, in high-risk, HER2-positive early non-metastatic breast cancer.

Study identification

NCT ID
NCT05113251
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
927 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 25, 2021 (Actual)
Primary completion
Mar 12, 2025 (Actual)
Completion
Apr 30, 2027 (Estimated)
Last update posted
Aug 11, 2026

2021 – 2027

United States locations

U.S. sites
22
U.S. states
16
U.S. cities
22
Facility City State ZIP Site status
Research Site Springdale Arkansas 72762 —
Research Site Beverly Hills California 90211 —
Research Site Glendale California 91204 —
Research Site Los Alamitos California 90720 —
Research Site Orange California 92868 —
Research Site New Haven Connecticut 06510 —
Research Site Fort Wayne Indiana 46804 —
Research Site Lexington Kentucky 40503 —
Research Site Louisville Kentucky 40202 —
Research Site Shreveport Louisiana 71101 —
Research Site Minneapolis Minnesota 55407 —
Research Site Las Vegas Nevada 89102 —
Research Site East Brunswick New Jersey 08816 —
Research Site Summit New Jersey 07901 —
Research Site Commack New York 11725 —
Research Site Durham North Carolina 27710 —
Research Site Greenville South Carolina 29607 —
Research Site Germantown Tennessee 38138 —
Research Site Nashville Tennessee 37203 —
Research Site Fort Worth Texas 76104 —
Research Site Ogden Utah 84405 —
Research Site Tacoma Washington 98405 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 123 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05113251, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 11, 2026 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05113251 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →