AL Amyloidosis Clinical Trial

Phase 1/2 Study of ZN-d5 for the Treatment of Relapsed or Refractory Light Chain (AL) Amyloidosis

Summary

This is a single arm, Open-Label, Phase 1/2 Study of ZN-d5 for the Treatment of Relapsed or Refractory Light Chain (AL) Amyloidosis.

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Full Description

A Single Arm, Open-Label, Phase 1/2 Study of ZN-d5 for the Treatment of Relapsed or Refractory Light Chain (AL) Amyloidosis. The first part of the study is phase 1 dose-escalation and the second part will be phase 2.

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Eligibility Criteria

Key Inclusion Criteria:

Diagnosis of AL amyloidosis based on histopathology, the presence of characteristic appearance on electron microscopy, or mass spectrometry typing of amyloid.
Prior AL amyloidosis treatment and has received at least one, but no more than three lines of prior therapy;
At least 3 months from hematopoietic stem cell transplantation or the shorter of 60 days or 5 half-lives for biologics, small molecules, or investigational drugs prior to starting treatment;
Measurable disease defined by serum differential free light chain;
Assessment of t(11,14) status by FISH;
Eastern Cooperative Oncology Group performance status ≤2 ;
History of organ involvement
Adequate bone marrow function prior to first administration of study drug;
Adequate organ function;

Key Exclusion Criteria:

Presence of non-AL amyloidosis, including wild-type or mutated ATTR amyloidosis;
Diagnosis of multiple myeloma according to the 2014 International Myeloma Working Group diagnostic criteria;
Mayo 2012 Stage IV disease;
Cardiac involvement exclusions apply to some subjects, including heart failure and cardiac arrhythmias.
Prior treatment with other BCL-2 inhibitors;

Study is for people with:

AL Amyloidosis

Phase:

Phase 1

Estimated Enrollment:

135

Study ID:

NCT05199337

Recruitment Status:

Active, not recruiting

Sponsor:

K-Group Alpha, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals, Inc.

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There are 12 Locations for this study

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University of Southern California
Los Angeles California, 90089, United States
Colorado Blood Cancer Institute
Denver Colorado, 80218, United States
Tulane University
New Orleans Louisiana, 70112, United States
Washington University
Saint Louis Missouri, 63130, United States
Tennessee Oncology
Nashville Tennessee, 37203, United States
Blackwater (Westmead) Hospital
Westmead New South Wales, 2145, Australia
Princess Alexandra Hospital
Brisbane Queensland, 4102, Australia
Royal Adelaide Hospital
Adelaide South Australia, 5000, Australia
Sir Charles Gairdner Hospital
Nedlands Western Australia, , Australia
Bank of Cyprus Hospital
Nicosia , , Cyprus
National and Kapodistrian University of Athens
Athens , 115 2, Greece
Rambam Hospital
Haifa , 31096, Israel
Hadassah Medical Center
Jerusalem , , Israel
Sheba Medical Center
Tel Aviv , , Israel
Tel Aviv Sourasky Medical Center PPDS
Tel Aviv , , Israel
IRCCS Azienda Ospedaliero Universitaria di Bologna Policlinico Sant'Orsola Malpighi
Bologna , , Italy
Fondazione I.R.C.C.S. Policlinico San Matteo
Pavia , , Italy
ICO Badalona-H.U. Germans Trias i Pujol
Barcelona Badalona, , Spain
Hospital Clínico Universitario Virgen de la Arrixaca
El Palmar Murcia, 30120, Spain
Hospital Clinic de Barcelona
Barcelona , 08036, Spain
Clinico de Salamanca
Salamanca , , Spain

How clear is this clinincal trial information?

Study is for people with:

AL Amyloidosis

Phase:

Phase 1

Estimated Enrollment:

135

Study ID:

NCT05199337

Recruitment Status:

Active, not recruiting

Sponsor:


K-Group Alpha, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals, Inc.

How clear is this clinincal trial information?

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