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NCT04538742Active, not recruitingPhase 1/2

A Phase 1b/2 Study of T-DXd Combinations in HER2-positive Metastatic Breast Cancer

A Phase 1b/2 Multicentre, Open-label, Modular, Dose-finding and Dose-expansion Study to Explore the Safety, Tolerability, and Anti-tumour Activity of Trastuzumab Deruxtecan (T-DXd) in Combination With Other Anti-cancer Agents in Patients With HER2-positive Metastatic Breast Cancer (DESTINY-Breast07)

Source: ClinicalTrials.gov · Last updated 8 Dec 2025

Brief summary (registry, in English)

DESTINY-Breast07 will investigate the safety, tolerability, and anti-tumour activity of trastuzumab deruxtecan (T-DXd) in combination with other anti-cancer agents in patients with HER2-positive Metastatic Breast Cancer

Status (registry)
Active, not recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
245 (actual)
First submitted
31 Aug 2020
Start date
28 Dec 2020
Primary completion date
31 Jan 2025
Lead sponsor
AstraZeneca
NCT number
NCT04538742
EU CT number
2023-505309-18-00
EudraCT number
2019-004531-22

What you commit to

  • Study type: Interventional · Phase 1/2
  • Participants enrolled: 245
  • From 28 Dec 2020 to the primary completion date, 31 Jan 2025
  • 45 sites in 15 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Active or prior documented (non-infectious) ILD/pneumonitis that required steroids, or suspected ILD/pneumonitis that cannot be ruled out by imaging at screening
  • Prior treatment with immune checkpoint inhibitors
  • Prior treatment with an ADC containing a topoisomerase I inhibitor
  • Prior treatment with tucatinib
    • CNS Exclusion
  • Module 6 and 7: Ongoing use of systemic corticosteroids for control of symptoms of brain metastases at a total daily dose of \> 2 mg dexamethasone or any brain lesion thought to require immediate local therapy

Other illness

  • Uncontrolled or significant cardiovascular disease
  • Lung-specific intercurrent clinically significant illnesses
  • Uncontrolled infection requiring IV antibiotics, antivirals, or antifungals
  • Spinal cord compression or a history of leptomeningeal carcinomatosis

Other

  • Modules 0 - 5: Has untreated brain metastasis

Who the study is looking for

  • Patients must be at least 18 years of age
  • Pathologically documented breast cancer that:
    • Is advanced/unresectable (patients that can be treated with curative intent are not eligible) or metastatic
    • HER2-positive (IHC 3+ or IHC 2+/ISH+) based on local assessment. The local HER2 result must be from a tumour sample obtained in the metastatic setting.
    • Is documented as hormone receptor-positive (estrogen or progesterone receptor) or negative in the metastatic setting
  • Patient must have adequate tumor sample from the metastatic setting for biomarker assessment
  • ECOG Performance Status of 0 or 1
  • Part 1
    • Disease progression on or after the last systemic therapy prior to starting study treatment
    • At least 1 prior treatment line in metastatic setting required.
  • Part 2 (Modules 0 - 5)
    • No prior lines of therapy for advanced/MBC allowed
  • Part 2 (Module 6 and 7) a) Zero or one prior lines of therapy for advanced/MBC allowed
    • CNS Inclusion
  • Modules 0 - 5 Patients must have no brain metastases or stable brain metastases.
  • Module 6 and 7 Patients must have untreated brain metastases not needing local therapy or previously treated brain metastases that have progressed since prior local therapy

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (45)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Research Site
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MelbourneAustraliaUnknown status
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BarretosBrazilUnknown status
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Belo HorizonteBrazilUnknown status
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NatalBrazilUnknown status
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Porto AlegreBrazilUnknown status
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Rio de JaneiroBrazilUnknown status
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São PauloBrazilUnknown status
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SorocabaBrazilUnknown status
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MontrealCanadaUnknown status
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QuébecCanadaUnknown status
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TorontoCanadaUnknown status
Klinikum rechts der Isar der TU Muenchen AöR
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MunichGermanyCompleted
Hospital del Mar
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BarcelonaSpainActive, not recruiting
Institut Catala D'oncologia
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L'Hospitalet de LlobregatSpainActive, not recruiting
Hospital Universitario HM Sanchinarro
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MadridSpainActive, not recruiting
University Hospital Virgen Del Rocio S.L.
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SevillaSpainActive, not recruiting
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VillejuifFranceUnknown status
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Buckhurst HillUnited KingdomUnknown status
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DelhiIndiaUnknown status
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GūrgaonIndiaUnknown status
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MaduraiIndiaUnknown status
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MumbaiIndiaUnknown status
Azienda Ospedaliero-Universitaria Di Bologna IRCCS Istituto Di Ricerca E Di Cura A Carattere Scientifico
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BolognaItalyActive, not recruiting
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BusanSouth KoreaUnknown status
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SeoulSouth KoreaUnknown status
Centrum Onkologii Im. Prof. Franciszka Lukaszczyka W Bydgoszczy
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BydgoszczPolandActive, not recruiting
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MoscowRussiaUnknown status
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Saint PetersburgRussiaUnknown status
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Hualien CityTaiwanUnknown status
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TainanTaiwanUnknown status
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TaipeiTaiwanUnknown status
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Taoyuan CityTaiwanUnknown status
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ColumbusUnited StatesUnknown status
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CommackUnited StatesUnknown status
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FairfaxUnited StatesUnknown status
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Fort MyersUnited StatesUnknown status
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Fort WorthUnited StatesUnknown status
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HarrisonUnited StatesUnknown status
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NashvilleUnited StatesUnknown status
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New YorkUnited StatesUnknown status
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St. PetersburgUnited StatesUnknown status
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AnkaraTurkey (Türkiye)Unknown status
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EdirneTurkey (Türkiye)Unknown status
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IstanbulTurkey (Türkiye)Unknown status
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IzmirTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.