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Clinical Trials in the UK / NCT04538742
Active, not recruiting Phase 1/2

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

NCT04538742 · tracked via the Priya Life Science UK tracker
Sponsor
AstraZeneca
Phase
Phase 1/2
Started
2020-12-28
Last updated
2025-12-08

Condition(s) studied

Metastatic Breast Cancer

Investigational drug(s) / intervention(s)

Trastuzumab deruxtecanDurvalumabPaclitaxelPertuzumabTucatinib

Trastuzumab deruxtecan: T-DXd: administered as an IV infusion

Durvalumab: Durvalumab: administered as an IV infusion

Paclitaxel: Paclitaxel: administered as an IV infusion

Pertuzumab: Pertuzumab: administered as an IV infusion

Tucatinib: Tucatinib administered orally (tablet) twice daily

Study summary

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

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Key Inclusion Criteria: * Patients must be at least 18 years of age * Pathologically documented breast cancer that: 1. Is advanced/unresectable (patients that can be treated with curative intent are not eligible) or metastatic 2. 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. 3. 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 1. Disease progression on or after the last systemic therapy prior to starting study treatment 2. At least 1 prior treatment line in metastatic setting required. * Part 2 (Modules 0 - 5) a) 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 Key Exclusion Criteria: * Uncontrolled or significant cardiovascular disease * Active or prior documented (non-infectious) ILD/pneumonitis that required steroids, or suspected ILD/pneumonitis that cannot be ruled out by imaging at screening * Lung-specific intercurrent clinically significant illnesses * Uncontrolled infection requiring IV antibiotics, antivirals, or antifungals * Spinal cord compression or a history of leptomeningeal carcinomatosis * Prior treatment with immune checkpoint inhibitors * Prior treatment with an ADC containing a topoisomerase I inhibitor * Prior treatment with tucatinib CNS Exclusion * Modules 0 - 5: Has untreated brain metastasis * 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

Primary outcome measure(s)

Trial sites (72)

FacilityCityRegionStatus
Research Site Fort Myers Florida
Research Site St. Petersburg Florida
Research Site Commack New York
Research Site Harrison New York
Research Site New York New York
Research Site New York New York
Research Site Columbus Ohio
Research Site Nashville Tennessee
Research Site Fort Worth Texas
Research Site Fairfax Virginia
Research Site Melbourne Australia
Research Site Barretos Brazil
Research Site Belo Horizonte Brazil
Research Site Natal Brazil
Research Site Porto Alegre Brazil
Research Site Porto Alegre Brazil
Research Site Rio de Janeiro Brazil
Research Site São Paulo Brazil
Research Site São Paulo Brazil
Research Site Sorocaba Brazil
Research Site Montreal Quebec
Research Site Québec Quebec
Research Site Toronto Canada
Research Site Villejuif France
Research Site München Germany
Research Site Würzburg Germany
Research Site Delhi India
Research Site Gurgaon India
Research Site Madurai India
Research Site Mumbai India
Research Site Bologna Italy
Research Site Milan Italy
Research Site Naples Italy
Research Site Rome Italy
Research Site Bydgoszcz Poland
Research Site Koszalin Poland
Research Site Lodz Poland
Research Site Lublin Poland
Research Site Moscow Russia
Research Site Moscow Russia

+ 32 more sites — see the full list on the official registry below.

On this site

📄 Enhertu (trastuzumab deruxtecan) drug profile → 📄 Imfinzi (durvalumab) drug profile →

More AstraZeneca trials in the UK

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04538742 on ClinicalTrials.gov ↗ ← All trials in the UK