Beta-amyloid PET/CT to See If AL-CA Therapy Works
Official title: A Follow-Up Study to Monitor Therapeutic Response in Light Chain Cardiac Amyloidosis Using Beta-amyloid PET/CT
Run by Peking Union Medical College Hospital · NCT07829705 · Data updated 2026-11-12
This study tests whether beta-amyloid PET/CT scans can show if treatment for light chain cardiac amyloidosis is helping after about a year.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Peking Union Medical College Hospital Academic / other |
| Drugs / interventions | Daratumumab |
| Locations | 1 site (Beijing) |
| Status | Recruiting |
| Started | June 3, 2020 |
| Main results expected | July 1, 2025 |
| Study ends | December 31, 2027 |
| Registry record updated | September 21, 2026 |
| Trial ID | NCT07829705 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) with newly diagnosed AL-CA who have started first-line plasma cell–directed or targeted therapies and can consent.
✕Probably not a fit
Patients without a measurable change in cardiac amyloid on imaging or with non-amyloid-related cardiac issues may see limited benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
In this Phase 2, single-center study, researchers use beta-amyloid PET/CT imaging to look for changes in amyloid burden after one year of therapy for AL-CA. They collect demographics, clinical data, and PET imaging to characterize any treatment-related changes from baseline. The goal is to determine if these molecular imaging markers reflect therapeutic response beyond standard biomarkers and imaging. Outcomes focus on whether amyloid burden reduction corresponds to clinical improvements.
Why it matters
Potential benefit: If successful, patients may receive a more precise imaging tool to monitor treatment response and tailor therapy.
How similar studies have gone: Prior work with beta-amyloid tracers in cardiac amyloidosis supports their potential to quantify amyloid burden, but this specific approach is still exploratory.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Age ≥ 18 y; 2. were proven newly diagnosed AL-CA by standard criteria; 3. subsequently received first-line therapies including anti-plasma cell therapy or targeted therapy; 4. must have given written informed consent (signed and dated) and any authorizations required by local law and be able to comply with all study requirements. Exclusion Criteria: 1. received therapy with an approved treatment (e.g., Bortezomib, Daratumumab) prior to enrollment; 2. pregnancy or breastfeeding; 3. severe claustrophobia; 4. any condition deemed by the investigator to interfere with study results or increase participant risk.
Where it's running
-
Peking Union Medical College Hospital
Beijing, China Recruiting
Study contacts
- Study coordinator: Li Huo
- Email: huoli@pumch.cn
- Phone: +86 18612672038
Similar studies
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.