Clinical trial · Interventional
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
NCT05199337CI-TRIAL-00080701completedPhase 1 / Phase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| AL Amyloidosis | AL Amyloidosis | ONTOLOGY_EXACT | 0.98 |
| Amyloidosis | Amyloidosis | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| ZN-d5 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Treatment Arm
- description
- Subjects will receive ZN-d5 orally (PO), once (QD) on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.
- interventionNames
- Drug: ZN-d5
Primary outcomes (2)
- measure
- Safety and Tolerability
- timeFrame
- 18 Months
- description
- Incidence and severity of adverse events (AEs), graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 5.0
- measure
- Dose limiting toxicities
- timeFrame
- 18 Months
- description
- Incidence of Dose-limiting toxicities (DLTs) observed in DLT evaluable subjects
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Key Inclusion Criteria: 1. Diagnosis of AL amyloidosis based on histopathology, the presence of characteristic appearance on electron microscopy, or mass spectrometry typing of amyloid. 2. Prior AL amyloidosis treatment and has received at least one, but no more than three lines of prior therapy; 3. 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; 4. Measurable disease defined by serum differential free light chain; 5. Assessment of t(11,14) status by FISH; 6. Eastern Cooperative Oncology Group performance status ≤2 ; 7. History of organ involvement 8. Adequate bone marrow function prior to first administration of study drug; 9. Adequate organ function; Key Exclusion Criteria: 1. Presence of non-AL amyloidosis, including wild-type or mutated ATTR amyloidosis; 2. Diagnosis of multiple myeloma according to the 2014 International Myeloma Working Group diagnostic criteria; 3. Mayo 2012 Stage IV disease; 4. Cardiac involvement exclusions apply to some subjects, including heart failure and cardiac arrhythmias. 5. Prior treatment with other BCL-2 inhibitors;
References
Publications (1)
- DERIVEDLocke M, Nieto M. AL Amyloidosis: Current Treatment and Outcomes. Adv Hematol. 2025 Mar 3;2025:7280805. doi: 10.1155/ah/7280805. eCollection 2025. PMID 40226119