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A disorder characterized by the localized or diffuse accumulation of amyloid protein in various anatomic sites. It may be primary, due to clonal plasma cell proliferations; secondary, due to long standing infections, chronic inflammatory disorders, or malignancies; or familial. It may affect the nerves, skin, tongue, joints, heart, liver, spleen, kidneys and adrenal glands.
Biomarker and diagnostic research for amyloidosis has been reported in the published literature.
Estimated prevalence: Unknown (Unknown prevalence).
301 clinical trials registered, 155 recruiting. Interventions under study include other interventions, drug therapy, biologic therapy, and procedural interventions. Pipeline includes 11 PHASE4, 31 PHASE3, 42 PHASE2. Research is sponsored by a mix of industry and academic institutions.
NCT ID | Title | Phase | Sponsor | Status |
|---|---|---|---|---|
[NCT07079423](https://clinicaltrials.gov/study/NCT07079423) |
Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 6:42 AM UTC
Patient Advocacy Groups (PAGs) provide support, resources, and community for patients and caregivers.
European rare disease database
Genetic and Rare Diseases Info Center
Teclistamab in Newly Diagnosed Mayo Stage IIIB AL Amyloidosis |
PHASE2 |
Peking Union Medical College Hospital |
RECRUITING |
[NCT06458374](https://clinicaltrials.gov/study/NCT06458374) | ATTR Cardiac Amyloidosis in a Selected Population | — | Helse Møre og Romsdal HF | RECRUITING |
[NCT07223203](https://clinicaltrials.gov/study/NCT07223203) | TRITON-PN: A Study to Evaluate the Efficacy and Safety of Nucresiran in Patients With Hereditary Transthyretin Amyloidosis With Polyneuropathy | PHASE3 | Alnylam Pharmaceuticals | RECRUITING |
[NCT07154381](https://clinicaltrials.gov/study/NCT07154381) | Hybrid Florbetaben PET/MRI for Imaging of Cardiac Amyloidosis | — | University Hospital, Essen | RECRUITING |
[NCT06192979](https://clinicaltrials.gov/study/NCT06192979) | Optimize First-line Treatment for AL Amyloidosis With t (11; 14) | NA | Jin Lu, MD | RECRUITING |
500 publications have been identified in PubMed for amyloidosis. Research spans Review / Meta-Analysis (37%), Basic Science / Preclinical (17%), and Epidemiology / Natural History (15%).
Research Type | Count | % of Total |
|---|---|---|
Research summaries | 186 | 37% |
Laboratory research | 83 | 17% |
Disease patterns and progression | 73 | 15% |
Patient case studies | 51 | 10% |
Clinical study results | 50 | 10% |
Testing and diagnosis research | 48 | 10% |
New treatment approaches | 6 | 1% |
Other research | 3 | 1% |
Sinigiani G (2026). [PMID: 41168058](https://pubmed.ncbi.nlm.nih.gov/41168058/). *Eur J Intern Med*. [Review / Meta-Analysis]
Kafil TS (2026). [PMID: 41236415](https://pubmed.ncbi.nlm.nih.gov/41236415/). *Curr Opin Cardiol*. [Review / Meta-Analysis]
Grabher BJ (2026). [PMID: 41667282](https://pubmed.ncbi.nlm.nih.gov/41667282/). *J Nucl Med Technol*. [Review / Meta-Analysis]
Yamamoto N (2026). [PMID: 41962876](https://pubmed.ncbi.nlm.nih.gov/41962876/). *Biochim Biophys Acta Proteins Proteom*. [Basic Science / Preclinical]
Fontana M (2026). [PMID: 41212997](https://pubmed.ncbi.nlm.nih.gov/41212997/). *Circulation*. [Clinical Trial Publication]
Razvi Y (2026). [PMID: 41528278](https://pubmed.ncbi.nlm.nih.gov/41528278/). *JACC Heart Fail*. [Diagnostic / Biomarker]
Meier C (2026). [PMID: 42041978](https://pubmed.ncbi.nlm.nih.gov/42041978/). *J Cardiovasc Dev Dis*. [Review / Meta-Analysis]
Kind A (2026). [PMID: 42197844](https://pubmed.ncbi.nlm.nih.gov/42197844/). *Sensors (Basel)*. [Review / Meta-Analysis]
Katzianer DS (2026). [PMID: 40945551](https://pubmed.ncbi.nlm.nih.gov/40945551/). *Cardiovasc Pathol*. [Epidemiology / Natural History]
Giamundo DM (2026). [PMID: 40985278](https://pubmed.ncbi.nlm.nih.gov/40985278/). *Eur J Clin Invest*. [Review / Meta-Analysis]
AI-curated news mentioning amyloidosis
Updated Sep 15, 2026
Helen Lachmann discusses the challenges in amyloidosis care, emphasizing the gap between drug approval and patient access due to health economics. She advocates for international collaboration to improve treatment for this ultra-rare disease.
A study highlights the complementary value of echocardiographic global longitudinal strain imaging and bone scintigraphy in cardiac screening for amyloid transthyretin (TTR) pathogenic variant carriers. This research could enhance early detection and management strategies for affected individuals.
Recent research highlights cystic fibrosis-associated amyloid A amyloidosis as a rare but severe complication with a poor prognosis. This discovery underscores the need for increased awareness and potential therapeutic strategies for affected patients.
Recent research highlights the dual involvement of cardiac and neurologic systems in amyloidosis, emphasizing the need for comprehensive management strategies. This study provides insights into the pathophysiology of the disease, which could inform future therapeutic approaches.