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Recruiting

NCT Number: NCT06610825

Castrate Resistant Prostate Cancer Enhertu Therapy

Use of Enhertu as a Subsequent Line of Therapy in HER2-Positive Metastatic Castration-Resistant Prostate Adenocarcinoma.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Phase 2

Primary location

Washington DC VAMC

Washington D.C., District of Columbia, 20422, United States

Location status: Recruiting

Location contact

Asha Escobar

CONTACT

[email protected]

2027431090

Maneesh Jain, MD

PRINCIPAL_INVESTIGATOR

About this study

This Phase II clinical trial aims to evaluate the efficacy and safety of Enhertu in HER-2 positive mCRPC who have progressed on prior androgen deprivation therapy and novel hormonal agents, who are either not candidates for or have refused taxane based chemotherapy. Led by Dr. Maneesh Jain at the Washington DC VA, the open label multi center study will include 60 participants treated with Enhertu. Primary endpoints focus on objective response rates, while secondary measures include safety, progression-free survival, overall survival, and quality of life.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pathologically confirmed adenocarcinoma of the prostate
  • Diagnosis of mCRPC
  • Documented progression on androgen deprivation and novel hormonal agents, with or without progression on taxane containing regimen
  • Ongoing ADT to maintain serum testosterone levels below 50 ng/dL
  • Formalin fixed paraffin embedded tumor tissue for HER2 immunohistochemistry
  • Life expectancy 6 months
  • ECOG 0 or 1
  • LVEF at least 50%
  • Adequate Blood Clotting function
  • Adequate Organ and Bone Marrow function
  • Adequate Renal function
  • Adequate Hepatic function

Exclusion criteria

  • History of interstitial lung disease or pneumonitis requiring steroids
  • Significant coronary vascular disease
  • Previous exposure to HER2 targeted therapy

Treatment and study plan

Enhertu

Drug

This is an open label, multi-center, single arm, phase II study designed to investigate the anti-tumor activity, efficacy and safety of Enhertu in HER2-positive metastatic castrate-resistant prostate cancer patients who progressed on androgen deprivation therapy and novel hormonal agents (such as Abiraterone and Enzalutamide), who also progressed, refused, or were not candidates to receive taxane-based chemotherapy.

Primary outcomes

  1. ORR

    Time frame: 2 years

    Objective Response Rate by local review, combining radiographic and biochemical responses

Secondary outcomes

  1. Progression Free Survival

    Time frame: 2 years

  2. Overall Survival

    Time frame: 2 years

  3. Disease Control Rate

    Time frame: 2 years

  4. Duration of Response

    Time frame: 2 years

Study contacts

Contact information is provided by the study sponsor or research team.

Asha Escobar

CONTACT

[email protected]

2027431090

Martha Antonio

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Washington D.C. Veterans Affairs Medical Center

Fed

Collaborators

  • Cancer Research And Biostatistics
  • Daiichi Sankyo
  • Institute for Clinical Research

Registry information

Official study title

A Phase II Clinical Trial to Evaluate the Efficacy and Safety of Fam-Trastuzumab Deruxtecan-Nxki (T-DXd) as a Subsequent Line of Therapy in HER2-Positive Metastatic Castration-Resistant Prostate Adenocarcinoma

Acronym: CaRPET

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Sep 24, 2024
Registry last updated
Apr 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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