ESPERANZA: External Control Arm Study for T-DXd for Patients with HER2 IHC3+ Solid Tumors

Study identifier:D967VR00001

ClinicalTrials.gov identifier:NCT06973161

EudraCT identifier:N/A

CTIS identifier:N/A

Recruiting

Official Title

External Control Arm Study for T-DXd for Patients with HER2 IHC3+ Solid Tumors (ESPERANZA)

Medical condition

Bladder Cancer

Phase

N/A

Healthy volunteers

Study drug

Sex

All

Estimated Enrollment

384

Study type

Observational

Age

18 Years - 130 Years

Date

Study Start Date: 10 Jun 2025

Estimated Primary Completion Date: 03 Nov 2025

Estimated Study Completion Date: 03 Nov 2025

Study design

Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Jul 2025 by AstraZeneca

Collaborators

Daiichi Sankyo, IQVIA

Inclusion and exclusion criteria

Inclusion Criteria

(for the ECA):
Male or female patients aged 18 years or older at the time of locally advanced, unresectable or metastatic disease diagnosis.
Patients diagnosed with one of the following malignancies:
Locally advanced, unresectable or metastatic colorectal adenocarcinoma, biliary tract, bladder (urothelial), cervical, endometrial, epithelial ovarian, pancreatic, or other solid tumors, or unresectable and/or metastatic non-squamous NSCLC.
Patients may be included on the basis of de-novo locally advanced, unresectable or metastatic disease diagnosis or progression from initial diagnosis at earlier stages.
Patients must have received at least one line of prior systemic anti-cancer therapy (SACT) therapy in the advanced/ unresectable/ metastatic setting (i.e. excluding adjuvant/ neoadjuvant SACT) prior to index.
Index date (start of 2nd or later line SoC systemic anti-cancer therapy (SACT) treatment) for advanced disease occurring between January 2017 and December 2022.
[CRC patients only] Prior treatment at index with at least one of the following in prior lines of therapy:
Fluoropyrimidine, oxaliplatin, and irinotecan
Anti-epidermal growth factor receptor (EGFR) treatment, if RAS wild-type
Anti-vascular endothelial growth factor (VEGF) treatment
Anti-programmed death-ligand 1 (PD-[L]-1) therapy if tumor is microsatellite instable (MSI)-high/deficient mismatch repair (dMMR), or tumor mutational burden (TMB)-high
[CRC patients only] BRAF wild-type cancer and confirmed RAS status (either mutant or wild type) identified through testing of the primary tumor or metastatic site at any time following initial diagnosis.
IHC3+ HER2-expression confirmed through testing of tumor samples taken in the advanced/ recurrent/ metastatic disease stage. The sample taken closest in time prior to the or at start of the index line of therapy should be used to confirm IHC3+ HER2 status. Positive IHC3+ tests may be the result of testing at the time of sampling by the sites or retrospective testing based on archival tumor samples
ECOG of 0 or 1 (or Karnofsky score of ≥ 70%8), or missing performance status based on most recently recorded information prior to or at index date.
Patients without recorded history of liver disease, leukaemia, aplastic anaemia or haemophilia at index date.
Patients known to have died must have a complete recorded date of death.

Exclusion Criteria

(for the ECA):
Record of other primary malignancies (except non-melanoma skin cancer) at any time prior to or after index.
Record of spinal cord compression prior to or at index or active CNS metastases at index (with active CNS metastases determined per physician judgment OR receipt of radiotherapy directed at CNS metastases within 6 months prior to index).
Record of myocardial infarction within 6 months prior to index date or congestive heart failure at any time prior to or at index date.
Record of lung-specific intercurrent clinically significant illness based on physician judgement prior to or at index date.
History of (non-infectious) ILD/ pneumonitis prior to or at index.
Record of autoimmune, connective tissue or inflammatory disorders prior to or at index date.
Record of complete pneumonectomy prior to or at index date.
Presence of systemic infection at index date.
Record of HIV prior to or at index date, or active Hep B or Hep C infection at index date.
Treatment with T-DXd or DXd-containing ADC at any time prior to or at index.
Record of pregnancy at or at any time following advanced/ unresectable/ metastatic disease diagnosis.
Treatment as part of a clinical trial at any time prior to or at index.
[Pan-tumor patients only] Patients with a record of pleural effusion, ascites or pericardial effusion that requires drainage, peritoneal shunt, or Cell-free and Concentrated Ascites Reinfusion Therapy (CART) at index.
[Colorectal patients only] Patients with record of leptomeningeal carcinomatosis prior to or at index.
[NSCLC patients only] Treatment with a HER2-targeted therapy (except for pan-HER class tyrosine kinase inhibitors) at any time prior to or at index.
[NSCLC patients only] Record of unstable angina at any time prior to or at index date.

Sort by status

No locations available

Arms	Assigned Interventions
Systemic Anticancer Therapy Patients who received the existing standard of care systemic anti-cancer therapy (SACT) per routine clinical practice in the real-world setting.	-
Trastuzumab Deruxtecan Patients who received 5.4 mg/kg trastuzumab deruxtecan	-

Documents available

Trial Results Summaries
Available here

Contacts

Contact

AstraZeneca Clinical Study Information Center

1-877-240-9479

[email protected]