Actively Recruiting

Age: 18Years - 130Years
All Genders
ID07124000

Effectiveness of Trastuzumab Deruxtecan Across HER2-positive Solid Tumors in Patients Without Alternative Treatments: A Hybrid Observational Study

Led by AstraZeneca · Updated on 2026-06-01

100

Participants Needed

17

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating trastuzumab deruxtecan (T-DXd) in patients with HER2-positive (IHC 3+) locally advanced, unresectable, or metastatic solid tumors who have received prior systemic treatment and have no satisfactory alternative treatment options. This observational study is conducted in the US, focusing on real-world settings with patients who have not been treated for breast, colorectal, non-small cell lung, gastric/gastroesophageal junction cancers, or hematological malignancies. The study aims to better understand treatment outcomes in routine clinical care. Participants receive trastuzumab deruxtecan monotherapy as part of their regular treatment based on the FDA label. The study involves about 100 patients enrolled at around 30 sites, including community oncology practices, hospitals, and academic centers. Patients are observed from the start of T-DXd treatment as determined by their clinician, without any experimental intervention assigned by the study. During the study, researchers collect data on tumor response and treatment duration, as well as the time to treatment discontinuation and the time to next treatment. Assessments are carried out through routine clinical evaluations, with follow-up lasting up to 2.5 years after enrollment. This approach helps capture real-world effectiveness and treatment patterns without additional procedures beyond usual care.

CONDITIONS

Brief Title

DESTINY-PANTUMOUR04

Who Can Participate

Age: 18Years - 130Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Diagnosed with locally advanced, unresectable, or metastatic HER2-positive (IHC 3+) solid tumors
  • Have received prior systemic treatment for metastatic or advanced disease
  • No satisfactory alternative treatment options as determined by the investigator
  • Clinician decision made to treat with trastuzumab deruxtecan (T-DXd) according to FDA label
  • HER2-positive status confirmed by local testing before enrollment
  • Able and willing to provide signed informed consent
Not Eligible

You will not qualify if you...

  • Primary diagnosis of breast adenocarcinoma, colorectal adenocarcinoma, non-small cell lung cancer, gastric or gastroesophageal junction adenocarcinoma, or hematological malignancies
  • Prior treatment with trastuzumab deruxtecan (T-DXd)
  • No baseline tumor burden assessment prior to starting T-DXd
  • Currently participating in another clinical trial at enrollment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - Up to 2.5 years after enrollment

Participants receive trastuzumab deruxtecan as part of routine clinical practice according to the FDA label.

Trial Site Locations

Total: 17 locations

1

Research Site

Birmingham, Alabama, United States, 35243

Actively Recruiting

2

Research Site

Bullhead City, Arizona, United States, 86442

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3

Research Site

Casa Grande, Arizona, United States, 85122

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4

Research Site

San Diego, California, United States, 92123

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5

Research Site

Boulder, Colorado, United States, 80309

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6

Research Site

Coral Springs, Florida, United States, 33065

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7

Research Site

St. Petersburg, Florida, United States, 33714

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8

Research Site

West Palm Beach, Florida, United States, 33401

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9

Research Site

Decatur, Illinois, United States, 62526

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10

Research Site

Topeka, Kansas, United States, 66604

Actively Recruiting

11

Research Site

Durham, North Carolina, United States, 27708

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12

Research Site

Wilson, North Carolina, United States, 27893

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13

Research Site

Canton, Ohio, United States, 44718

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14

Research Site

Maumee, Ohio, United States, 43537

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15

Research Site

Philadelphia, Pennsylvania, United States, 19104

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16

Research Site

Nashville, Tennessee, United States, 37203

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17

Research Site

Dallas, Texas, United States, 75390

Actively Recruiting

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Research Team

A

AstraZeneca Clinical Study Information Center

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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