Uremia
diseaseOn this page
Also known as uremia of renal origin
Summary
Uremia (MONDO:0007008) is a disease and 30 clinical trials. Top therapeutic interventions include ascorbic acid, basiliximab, and cysteine. A subtype of kidney failure — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 30
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | uremia |
| Mondo ID | MONDO:0007008 |
| EFO | EFO:1001226 |
| MeSH | D014511 |
| DOID | DOID:4676 |
| SNOMED CT | 44730006 |
| UMLS | C0041948 |
| MedGen | 12008 |
| MedDRA | 10046369 |
| Is cancer (heuristic) | no |
Also known as: uremia of renal origin
Disease family
This is a subtype of kidney failure. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by body system or component › urinary system disorder › kidney disorder › kidney failure › uremia
Related subtypes (2): acute kidney injury, chronic renal failure syndrome
Subtypes (1): uremic neuropathy
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
Drugs indicated for this disease
No approved or late-stage (phase ≥3) drug is indicated for this disease; the following are in earlier-phase trials only.
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Cysteine.
Clinical trials & evidence
Clinical trials
Clinical trials: 30.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 17 |
| PHASE4 | 7 |
| PHASE2 | 2 |
| PHASE1/PHASE2 | 2 |
| PHASE3 | 1 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06998732 | PHASE4 | NOT_YET_RECRUITING | BCD to Measure the ED95 of Remimazolam-Assisted Sedation in Arteriovenous Fistula Creation Surgery |
| NCT00317005 | PHASE4 | COMPLETED | Uremic Hyperhomocysteinemia -A Folate Trial for Possible Prevention of Cardiovascular Events |
| NCT00388648 | PHASE4 | COMPLETED | Very Low Protein Diet or Dialysis in Uremic Elderly? |
| NCT00442819 | PHASE4 | COMPLETED | Uremic Pruritus, Cytokines and Polymethylmethacrylate Artificial Kidney |
| NCT00649298 | PHASE4 | COMPLETED | A Clinical Trial of IntensiVE Dialysis |
| NCT01356433 | PHASE4 | COMPLETED | Influence of Oral Vitamin C Supplement on the Inflammation Status in Dialysis Patients |
| NCT05750875 | PHASE4 | COMPLETED | Gabapentin Versus Loratadine in Uremic Pruritus |
| NCT01583309 | PHASE3 | COMPLETED | Effects of Convective Therapies in Dialysis Patients |
| NCT01267760 | PHASE2 | COMPLETED | Clinical and Biochemical Effects of Multipass Hemodialysis |
| NCT01408797 | PHASE1/PHASE2 | UNKNOWN | Clonal Deletion on Living-Relative Donor Kidney Transplantation |
| NCT02050139 | PHASE2 | COMPLETED | L-Cysteine in Peritoneal Dialysis |
| NCT02492490 | PHASE1/PHASE2 | UNKNOWN | Effect of SVF Derived MSC in DCD Renal Transplantation |
| NCT05386433 | EARLY_PHASE1 | UNKNOWN | Paxlovid in the Treatment of COVID-19 Patients With Uremia |
| NCT03629977 | Not specified | RECRUITING | Timing of Renal Replacement Therapy in the Critically Ill Patients |
| NCT06233838 | Not specified | RECRUITING | Multi-center Clinical Study on Hemoperfusion of KHA80 |
| NCT07189741 | Not specified | NOT_YET_RECRUITING | Dynamic Breath VOC Profiling as a Non-invasive Tool to Assess Hemodialysis Adequacy |
| NCT00375635 | Not specified | UNKNOWN | Removal of Protein Bound Uremic Toxins by Modified Plasma Separation and Adsorption Combined With Hemodialysis |
| NCT00577967 | Not specified | UNKNOWN | Gabapentin - A Solution to Uremic Pruritus? |
| NCT01391884 | Not specified | COMPLETED | Elimination of Incretin Hormones in Patients With Severe Kidney Failure |
| NCT01766895 | Not specified | UNKNOWN | Long-term Follow Up of Viral Hepatitis in Uremic Patients in Taiwan |
| NCT02266238 | Not specified | UNKNOWN | Stenosis of Arteria-Venous Fistula in Maintenance Hemodialysis Patients: Early Intervention Trial |
| NCT02446535 | Not specified | UNKNOWN | Probing the Dry Weight (DW) by Bioimpedance (BIA): Which is the Gold Standard Between Clinical DW and BIA DW? |
| NCT02606955 | Not specified | UNKNOWN | Probing the Dry Weight by Bioimpedance: The Resistance Stabilization Test |
| NCT03416192 | Not specified | WITHDRAWN | 12 Weeks of Hemodialysis With Medium Cut-Off Filter Compared to Hemodiafiltration With Standard High-flux Filter. |
| NCT03437538 | Not specified | COMPLETED | Reduction Ratio and Clearance During Hemodialysis With MCO-filter Compared to HDF With Standard High-flux Filter |
| NCT04768309 | Not specified | COMPLETED | Impact of Intestinal Microbiota on Uremic Toxins Productions |
| NCT05076318 | Not specified | COMPLETED | Dysregulated Urea-synthesis at Terminal Uremia |
| NCT05899283 | Not specified | COMPLETED | A Comparative Study of Two Kinds of Hemodialysis Filters |
| NCT06875115 | Not specified | COMPLETED | Evaluation of the Efficacy of Laser Acupuncture on Uremic Pruritus |
| NCT07086430 | Not specified | COMPLETED | Independent Effects of Visceral Adipose Volume and Density on Patient Survival in Peritoneal Dialysis |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| ASCORBIC ACID | 4 | 1 |
| BASILIXIMAB | 4 | 1 |
| CYSTEINE | 4 | 1 |
| FOLIC ACID | 4 | 1 |
| LORATADINE | 4 | 1 |
| NIRMATRELVIR | 4 | 1 |
| REMIMAZOLAM | 4 | 1 |
Related Atlas pages
- Drugs: Ascorbic Acid, Basiliximab, Cysteine, Folic Acid, Loratadine, Nirmatrelvir, Remimazolam