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USClinicalTrials.govClinical trialPhase 3Active, not recruiting

Trastuzumab Deruxtecan (T-DXd) With or Without Pertuzumab Versus Taxane, Trastuzumab and Pertuzumab in HER2-positive Metastatic Breast Cancer (DESTINY-Breast09)

Official record

Identifier
NCT04784715
Recruiting locations

countries

United StatesArgentinaBelgiumBrazilCanadaChinaDenmarkFranceGermanyHungaryIndiaIsraelItalyJapanMexicoPeruPhilippinesRomaniaRussiaSaudi ArabiaSouth AfricaSouth KoreaSpainSwedenTaiwanTurkey (Türkiye)United Kingdom
Interventions studied
Trastuzumab deruxtecanPlaceboTaxanePertuzumabTrastuzumab
Lead sponsor
AstraZeneca
Target enrolment
1157 participants
Study type
INTERVENTIONAL
Phase
Phase 3
Status
Active, not recruiting
First posted
Mar 5, 2021
Last updated on the registry
Jul 30, 2026
Age
18 Years – 130 Years
Sex
ALL
Study contact
No public contact is listed on the official record.
Eligibility criteria

Reproduced verbatim from the official record. Eligibility is decided by the study team, never by this page.

Key Inclusion Criteria:

* Patients must be ≥18 years of age
* Pathologically documented breast cancer that:

  1. is advanced or metastatic
  2. is locally assessed and prospectively centrally confirmed as HER2-positive (IHC3+ or ISH+)
  3. is documented by local testing as hormone receptor (HR)-positive or HR-negative disease in the metastatic setting
* No prior chemotherapy or HER2-targeted therapy for advanced or metastatic breast cancer or only 1 previous line of endocrine therapy in the metastatic setting. Participants who have received chemotherapy or HER2-targeted therapy in the neo-adjuvant or adjuvant setting are eligible if \> 6 months from treatment to metastatic diagnosis.
* Has protocol-defined adequate organ and bone marrow function
* ECOG performance status 0 or 1

Key Exclusion Criteria:

* Ineligible for any of the agents on the study.
* Any substance abuse or other medical conditions that, in the investigator's opinion, may interfere with subject's participation or study results
* Patients with spinal cord compression or clinically active central nervous system metastases. Participants with clinically inactive brain metastases or treated brain metastases that are no longer symptomatic may be included in the study.
* Active or prior documented interstitial lung disease (ILD)/pneumonitis or suspected ILD/pneumonitis that cannot be ruled out by imaging at screening
* Prior randomization or treatment in a previous trastuzumab deruxtecan study regardless of treatment arm assignment
Indexed under
Breast Cancer

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