An Expanded Access Treatment Protocol of Zanidatamab (ZW25) in Patients With HER2-Positive Advanced Biliary Tract Cancer

• Conditions: HER2-Positive Advanced Biliary Tract Cancer

• Registration Number: NCT04578444
• Lead Sponsor: Jazz Pharmaceuticals

Brief Summary

This is an intermediate-size Expanded Access Protocol (EAP) for use of zanidatamab (ZW25) in patients with human epidermal growth factor receptor 2 (HER2)-positive advanced biliary tract cancer (BTC) who are not eligible for other zanidatamab clinical trials, and who in the opinion of the treating oncologist, would potentially benefit from treatment with zanidatamab.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2020-09-30
• Study First Submitted QC: 2020-09-30
• Study First Posted: 2020-10-08
• Status Verified: 2025-02
• Last Update Submitted: 2025-02-03
• Last Update Posted: 2025-02-04

Recruitment & Eligibility

• Status: AVAILABLE
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Histologically confirmed HER2-positive locally advanced or metastatic biliary tract cancer that has progressed after receipt of available therapies known to confer clinical benefit.
• Adequate cardiac left ventricular function, as defined by left ventricular ejection fraction (LVEF) ≥ 50%
• Adequate organ function
• Ineligible to participate or has no access to an ongoing zanidatamab or other Zymeworks clinical study (e.g., ZW49 clinical study).
• Females of childbearing potential and non-sterile males must agree to practice highly effective methods of birth control for the duration of the study and for 12 months after the last dose of study drug. In addition, non-sterile males must avoid sperm donation for the duration of the study and for 12 months after the last dose of study drug.

Exclusion Criteria

• Participating in other studies involving investigational drug(s) ≤ 3 weeks before the first dose of zanidatamab.

• Systemic anti-cancer therapy ≤ 3 weeks before the first dose of zanidatamab.

• Radiotherapy ≤ 2 weeks of the first dose of zanidatamab

• The following central nervous system (CNS) brain lesions are excluded from the study:

  • Untreated or unstable brain lesions requiring immediate local therapy or symptomatic CNS metastases.

  • Radiation treatment for CNS metastases within 4 weeks before the first dose of zanidatamab.

  • Known history of or ongoing leptomeningeal disease (LMD). If LMD has been reported radiographically, but is not suspected clinically by the investigator, the patient must be free of neurological symptoms of LMD.

  • The following CNS brain lesions are permitted:

    • Stable brain lesions are permitted if stable, as defined by patients who are off steroids and anticonvulsants and are neurologically stable with no evidence of radiographic progression for at least 4 weeks at the time of screening.

• Concurrent uncontrolled or active hepatobiliary disorders or untreated or ongoing complications after laparoscopic procedures or stent placement, including but not limited to active cholangitis, unresolved biliary obstruction, biloma or abscess. Any complications should be resolved within 2 weeks prior to the first dose of zanidatamab.

• Active hepatitis

• Infection with human immunodeficiency virus (HIV) with uncontrolled disease.

• Females who are breastfeeding or pregnant, and females and males planning a pregnancy.

• History of myocardial infarction or unstable angina within 6 months prior to enrollment, congestive heart failure (NYHA Class 3 or 4), or clinically significant cardiac disease

• QTc Fridericia (QTcF) > 470 ms assessed within 30 days of screening

• Acute or chronic uncontrolled pancreatitis or Child-Pugh Class C liver disease

Study & Design

• Study Type: EXPANDED_ACCESS
• Study Design: Not specified

Trial Locations

Locations (17)

NoCo Banner MD Anderson Cancer Center; 🇺🇸 Gilbert, Arizona, United States

TOI Clinical Research; 🇺🇸 Cerritos, California, United States

Salinas Valley Memorial Healthcare System; 🇺🇸 Salinas, California, United States

Washington University School of Medicine; 🇺🇸 Saint Louis, Missouri, United States

Jean Minjoz Hospital; 🇫🇷 Besançon, France

Hopital Timone Marseille; 🇫🇷 Marseille cedex 5, France

Hopital Haut-Leveque - CHU Bordeaux; 🇫🇷 Pessac, France

Gustave Roussy Cancer Center; 🇫🇷 Villejuif, France

ICCRS Candiolo; 🇮🇹 Candiolo, Italy

Istituto Nazionale Tumori; 🇮🇹 Milano, Italy

Istituto Clinico Humanitas; 🇮🇹 Milan, Italy

Vall D'Hebron University Hospital; 🇪🇸 Barcelona, Spain

Fundacion Jimenez Diaz University Hospital - Autonomous University of Madrid; 🇪🇸 Madrid, Spain

Hospital Universitario 12 de Octubre; 🇪🇸 Madrid, Spain

The Princess Alexandra Hospital NHS Trust (Joanne Kwa, Pharmacist); 🇬🇧 Harlow, United Kingdom

UCLH Cancer Institute (Meera Desai, Pharmacist); 🇬🇧 London, United Kingdom

HCA Healthcare UK; 🇬🇧 London, United Kingdom