For Healthcare Professionals

A Phase 1b Study of T-DXd Combinations in HER2-low Advanced or Metastatic Breast Cancer

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About the study

DESTINY-Breast 08 will investigate the safety, tolerability, PK and preliminary anti-tumour activity of T-DXd in combination with other therapies in patients with Metastatic HER2-low Advanced or Metastatic Breast Cancer
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Key Inclusion Criteria:


Patients must be at least 18 years of age


Male or female patients who have pathologically documented breast cancer that:


  1. Has a history of HER2-low expression, defined as IHC 2+/ISH- or IHC 1+ (ISH- or untested) with a validated assay
  2. Is documented as HR+ (either ER and/or PgR positive [ER or PgR ≥1%]) or ER and PgR negative (ER and PgR <1%) per ASCO/CAP guidelines in the metastatic setting
  3. Patient must have adequate tumor sample for biomarker assessment
  4. ECOG Performance Status of 0 or 1

For patients with HR+ disease:


Part 1: At least 1 prior treatment line of ET with or without a targeted therapy (such as CDK4/6, mTOR or PI3-K inhibitors), and at least 1 prior line of chemotherapy for MBC are required.


Part 2: Only 1 prior treatment line of ET with or without a targeted therapy (such as CDK4/6, mTOR or PI3-K inhibitors) for MBC is allowed. No prior chemotherapy in the metastatic setting is allowed. Note there are no patients with HR+ disease in Part 2 of Modules 2 and 3.


For patients with HR- disease:


Part 1: At least 1 prior line of chemotherapy for MBC is required. Note there are no patients with HR- disease in Part 1 of Modules 4 and 5.


Part 2: For Module 2, no prior lines of therapy for MBC are allowed, and for Modules 1 and 3, only 1 prior line of chemotherapy for MBC is allowed. Note there are no patients with HR- disease in Part 2 of Modules 4 and 5.


EXCLUSION CRITERIA

Key Exclusion Criteria:


  1. Uncontrolled intercurrent illness
  2. Uncontrolled or siginificant cardiovascular disease
  3. History of (non-infectious) ILD/pneumonitis that required steroids, has current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at screening.
  4. Lung-specific intercurrent clinically significant illnesses
  5. Has spinal cord compression or clinically active central nervous system metastases
  6. Active primary immunodeficiency
  7. Uncontrolled infection requiring IV antibiotics, antivirals, or antifungals
  8. Prior treatment with ADC that comprises of an exatecan derivative that is a topoisomerase I inhibitor.

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.

Study’s details


Contition

Metastatic Breast Cancer

Age (in years)

18+

Phase

Phase 1

Participants needed

139

Est. Completion Date

Nov 28, 2025

Treatment type

Interventional


Sponsor

AstraZeneca

ClinicalTrials.gov identifier

NCT04556773

Study number

D967JC00002

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