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Age: 18Years +
All Genders
ID05993234

A Prospective Non-interventional Study of Trastuzumab DeRuxtecan for Adults With Advanced HER2-positive Gastric or Gastroesophageal Junction Adenocarcinoma After Prior Trastuzumab Treatment, Including a Disease Registry of Conventional Therapies in Europe PROSPERITY

Led by Daiichi Sankyo Europe, GmbH, a Daiichi Sankyo Company · Updated on 2026-05-08

257

Participants Needed

76

Research Sites

39 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating trastuzumab deruxtecan T-DXd as a treatment for adult patients with advanced HER2-positive gastric or gastroesophageal junction GEJ adenocarcinoma who have previously received a trastuzumab-based regimen. This study aims to assess the real-world effectiveness of T-DXd, patient characteristics, treatment patterns, and safety in this population. It also includes data collection on patients receiving conventional therapies for exploratory comparison. This is a non-interventional observational study where patients receive T-DXd or conventional therapies as part of routine clinical care according to approved guidelines SmPC. No investigational drugs are given. The study tracks patients starting T-DXd as a second-line or later treatment and collects data on other therapies such as chemotherapy and immunotherapy used in clinical practice. Participants will be followed for up to approximately 2 years from baseline to monitor outcomes including time to next treatment, changes in treatment, physician-reported safety events, use of prophylactic treatments, and quality of life using validated questionnaires. Data on physician visits, treatment discontinuation, and safety events will also be collected to understand treatment tolerability and patient experience in a real-world setting.

CONDITIONS

Brief Title

A Study of Trastuzumab DeRuxtecan for Patients With Advanced HER2-pOsitive GaStric or GastroesoPhageal Junction AdEnocarcinoma Who Have Received a PrIor Trastuzumab-based Regimen Accompanied by a Disease RegistrY of Patients Treated With Conventional Therapies (PROSPERITY)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult male or female patients aged 18 years or older
  • Diagnosed with advanced HER2-positive gastric or gastroesophageal junction adenocarcinoma
  • Documented HER2-positive status from archival or recent samples prior to second-line therapy
  • Decision made to begin monotherapy with trastuzumab deruxtecan or conventional therapies according to physician's choice and SmPC
  • Provided written, dated, and signed informed consent to participate
Not Eligible

You will not qualify if you...

  • Currently participating in or previously participated in a blinded interventional study at the time of data collection
  • Pregnant or breastfeeding
  • No other specific exclusion criteria defined; patients treated according to SmPC indications

Research Team

C

Contact for Clinical Trial Information

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