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NCT05199337CompletedPhase 1/2

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

A Single Arm, Open-Label, Phase 1/2 Study of ZN-d5 for the Treatment of Relapsed or Refractory Light Chain (AL) Amyloidosis

Source: ClinicalTrials.gov · Last updated 19 Sept 2024

Brief summary (registry, in English)

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.

Status (registry)
Completed
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
18 (actual)
First submitted
9 Jan 2022
Start date
30 Nov 2021
Primary completion date
14 Feb 2024
Lead sponsor
K-Group Alpha, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals, Inc.
Diseases
Amyloidosis
NCT number
NCT05199337

What you commit to

  • Study type: Interventional · Phase 1/2
  • Participants enrolled: 18
  • From 30 Nov 2021 to the primary completion date, 14 Feb 2024
  • 21 sites in 7 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior treatment with other BCL-2 inhibitors;

Other illness

  • Mayo 2012 Stage IV disease;
  • Cardiac involvement exclusions apply to some subjects, including heart failure and cardiac arrhythmias.

Other

  • 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;

Who the study is looking for

  • 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;

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (21)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Royal Adelaide Hospital
Coordinator of this site? Confirm its status
AdelaideAustraliaUnknown status
Princess Alexandra Hospital
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BrisbaneAustraliaUnknown status
Sir Charles Gairdner Hospital
Coordinator of this site? Confirm its status
NedlandsAustraliaUnknown status
Blackwater (Westmead) Hospital
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WestmeadAustraliaUnknown status
Bank of Cyprus Hospital
Coordinator of this site? Confirm its status
NicosiaCyprusUnknown status
ICO Badalona - H.U. Germans Trias i Pujol
Coordinator of this site? Confirm its status
BarcelonaSpainUnknown status
Hospital Clinic de Barcelona
Coordinator of this site? Confirm its status
BarcelonaSpainUnknown status
Hospital Clínico Universitario Virgen de la Arrixaca
Coordinator of this site? Confirm its status
El PalmarSpainUnknown status
Clinico de Salamanca
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SalamancaSpainUnknown status
National and Kapodistrian University of Athens
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AthensGreeceUnknown status
Rambam Hospital
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HaifaIsraelUnknown status
Hadassah medical Center
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JerusalemIsraelUnknown status
Sheba Medical Center
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Tel AvivIsraelUnknown status
Tel Aviv Sourasky Medical Center PPDS
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Tel AvivIsraelUnknown status
IRCCS Azienda Ospedaliero-Universitaria di Bologna, Policlinico Sant'Orsola Malpighi
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BolognaItalyUnknown status
Fondazione I.R.C.C.S. Policlinico San Matteo
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PaviaItalyUnknown status
Colorado Blood Cancer Institute
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DenverUnited StatesUnknown status
University of Southern California
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Los AngelesUnited StatesUnknown status
Tennessee Oncology
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NashvilleUnited StatesUnknown status
Tulane University
Coordinator of this site? Confirm its status
New OrleansUnited StatesUnknown status
Washington University
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St LouisUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.