Charcoal, Activated
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Also known as Activated charcoalAst 120AST-120Carbo vegetabilisCarbonmedicinalCharcoalactivatedMedicinal carbonMedicinal charcoal
Summary
Charcoal, Activated (CHEMBL2106049) is a phase-3 clinical-stage small molecule (ATC A07BA01); indicated across 15 conditions including inflammatory bowel disease and chronic kidney disease.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Small molecule
- ATC class: A07BA01 (+1 more)
- Indications: 15 conditions
- Clinical trials: 58
- Chemistry: 16.043 Da · CH4
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL2106049 |
| Name | Charcoal, Activated |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 297 |
| ChEBI | CHEBI:27594 |
| ATC | A07BA01, A07BA51 |
| Molecular formula | CH4 |
| Molecular weight | 16.043 |
| InChIKey | VNWKTOKETHGBQD-UHFFFAOYSA-N |
SMILES: C
IUPAC name: methane
Pharmacological roles (ChEBI): macronutrient.
Also known as: Activated charcoal, Ast 120, AST-120, Carbo vegetabilis, Carbon, medicinal, Charcoal, activated, Medicinal carbon, Medicinal charcoal, CHARCOAL, ACTIVATED
Patent coverage: 4,335,983 distinct patent families (8,686,700 SureChEMBL compound mentions), from 61 matched compound structure(s). One matched structure accounts for 8,685,780 (100%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
No target linkage available.
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
15 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| inflammatory bowel disease | 3 | MONDO:0005265 | EFO:0003767 |
| chronic kidney disease | 3 | MONDO:0005300 | EFO:0003884 |
| gastric neoplasm | 3 | MONDO:0021085 | MONDO:0001056 |
| multiple sclerosis | 3 | MONDO:0005301 | MONDO:0005301 |
| irritable bowel syndrome | 2 | MONDO:0005052 | EFO:0000555 |
| pouchitis | 2 | MONDO:0005312 | EFO:0003921 |
| gastroesophageal reflux disease | 2 | MONDO:0007186 | EFO:0003948 |
| brain disorder | 2 | MONDO:0005560 | HP:0001298 |
| lung neoplasm | 2 | MONDO:0021117 | MONDO:0008903 |
| chronic obstructive pulmonary disease | 1 | MONDO:0005002 | EFO:0000341 |
| insomnia | 1 | MONDO:0013600 | EFO:0004698 |
| major depressive disorder | 1 | MONDO:0002009 | MONDO:0002009 |
| asthma | 1 | MONDO:0004979 | MONDO:0004979 |
| type 2 diabetes mellitus | 1 | MONDO:0005148 | MONDO:0005148 |
| allergic disease | 1 | MONDO:0005271 | MONDO:0005271 |
Clinical trials
Total trials: 58.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE1 | 18 |
| PHASE2 | 12 |
| Not specified | 11 |
| PHASE4 | 7 |
| PHASE3 | 7 |
| EARLY_PHASE1 | 2 |
| PHASE2/PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05471479 | PHASE4 | RECRUITING | Activated CHARcoal in Poisoned Patient - Pilot Trial |
| NCT07182422 | PHASE4 | RECRUITING | AST-120 (Kremezin®) for the Renal Protection and Attenuation of Decline in Acute Kidney Disease |
| NCT00860431 | PHASE4 | COMPLETED | Kremezin Study Against Renal Disease Progression in Korea |
| NCT01681303 | PHASE4 | COMPLETED | Effect of An Oral Absorbent AST-120 in Late-stage Chronic Kidney Disease (CKD) Patients. |
| NCT02969746 | PHASE4 | WITHDRAWN | Activates Charcoal for Patients Undergoing Invasive Procedure Delayed Due to Direct Oral Anticoagulants |
| NCT04639674 | PHASE4 | COMPLETED | AST-120 in Hemodialysis Patients With Uremic Pruritus |
| NCT06219967 | PHASE4 | COMPLETED | Does a Soft Drink Mixture Improve Tolerance of Activated Charcoal in the Adult Poisoned Patient Without Affecting Efficacy |
| NCT06141473 | PHASE3 | ACTIVE_NOT_RECRUITING | Efficacy and Safety Studies of Frexalimab (SAR441344) in Adults With Relapsing Forms of Multiple Sclerosis |
| NCT00321412 | PHASE3 | COMPLETED | Safety and Efficacy of AST-120 in Mild to Moderate Crohn’s Patients With Fistulas |
| NCT00500682 | PHASE3 | COMPLETED | A Study of AST-120 for Evaluating Prevention of Progression In Chronic Kidney Disease (EPPIC-1) |
| NCT00501046 | PHASE3 | COMPLETED | A Study of AST-120 for Evaluating Prevention of Progression In Chronic Kidney Disease Including Assessment of Quality of Life (EPPIC-2) |
| NCT00678366 | PHASE3 | COMPLETED | Evaluation of Adding Small Amounts of Oxygen to the CO2 Pneumoperitoneum Upon Pain and Inflammation |
| NCT01863888 | PHASE3 | COMPLETED | Effect of Teriflunomide on Immune Cell Subsets in the Blood of Patients With Multiple Sclerosis |
| NCT02123407 | PHASE3 | UNKNOWN | Clinical Study on the Harvesting Lymph Nodes With Carbon Nanoparticles for Advanced Gastric Cancer |
| NCT05540431 | PHASE2/PHASE3 | UNKNOWN | Evaluation of Protective Effect of Activated Charcoal and Probiotic Against Progression of Chronic Kidney Disease |
| NCT06579066 | PHASE2 | NOT_YET_RECRUITING | The Effect of Probiotics vs Activated Charcoal in the Management of CKD Patients Suffering From Uremic Pruritus. |
| NCT06906874 | PHASE2 | RECRUITING | Activated Charcoal Use in Chronic Kidney Disease Patients |
| NCT00558038 | PHASE2 | COMPLETED | Safety and Efficacy of AST-120 Compared to Lactulose in Patients With Hepatic Encephalopathy |
| NCT00583076 | PHASE2 | COMPLETED | Safety and Efficacy of AST-120 in the Treatment of Pouchitis |
| NCT00583128 | PHASE2 | COMPLETED | Safety and Efficacy of AST-120 in Patients With Non-Constipating Irritable Bowel Syndrome |
| NCT00583531 | PHASE2 | TERMINATED | Safety and Efficacy of AST-120 in the Treatment of Antibiotic-Refractory Pouchitis |
| NCT00587275 | PHASE2 | TERMINATED | Safety and Efficacy of AST-120 in Patients With GERD Who Continue to be Symptomatic on a Standard Dose of PPI |
| NCT00867698 | PHASE2 | COMPLETED | AST-120 Used to Treat Mild Hepatic Encephalopathy |
| NCT01811394 | PHASE2 | UNKNOWN | Ion Irradiation of Sacrococcygeal Chordoma |
| NCT04311645 | PHASE2 | UNKNOWN | Role of Activated Charcoal in Decreasing Blood Urea, Creatinine and Phosphorous |
| NCT04928950 | PHASE2 | WITHDRAWN | Charcoal in Lung Cancer Patients Undergoing TEMLA |
| NCT05229874 | PHASE2 | UNKNOWN | Effect of CNSI vs. ICG in Lymph Node Tracing During Gastrectomy |
| NCT00719758 | PHASE1 | COMPLETED | Drug-Drug Interaction Study of TRK-100STP |
| NCT01236105 | PHASE1 | COMPLETED | Effect of Activated Charcoal and Time of Dose on the Pharmacokinetics of LY2624803 in Healthy Subject |
| NCT01257191 | PHASE1 | COMPLETED | A Study to Compare the Effects of Different Sized Particles on Cells in the Nose |
| NCT01280175 | PHASE1 | COMPLETED | Foster With or Without Charcoal Block or Aerochamber Plus |
| NCT01389752 | PHASE1 | COMPLETED | A Study to Evaluate the Effect of Activated Charcoal on the Absorption of LY2216684 in Healthy Subjects |
| NCT01409369 | PHASE1 | COMPLETED | A Study on The Effect of Multiple Doses of Activated Charcoal on The Pharmacokinetics of a Single Dose of RO4995819 |
| NCT01593826 | PHASE1 | COMPLETED | Comparison of Absorption of Budesonide and Formoterol From Budesonide/Formoterol Easyhaler and Symbicort Turbuhaler |
| NCT01627158 | PHASE1 | COMPLETED | Pharmacokinetic Study Comparing Budesonide/Formoterol Easyhaler and Symbicort Turbuhaler Forte |
| NCT01766843 | PHASE1 | COMPLETED | Comparison of Salmeterol and Fluticasone Propionate Absorption From Salmeterol/Fluticasone Easyhaler and Seretide Diskus |
| NCT01856621 | PHASE1 | COMPLETED | Comparison of Salmeterol and Fluticasone Propionate Absorption From Salmeterol/Fluticasone Easyhaler With Seretide Diskus |
| NCT02657512 | PHASE1 | COMPLETED | Effect of Activated Charcoal on Rivaroxaban Pharmacokinetics in Healthy Subjects |
| NCT02691325 | PHASE1 | COMPLETED | Study to Evaluate the Safety, Tolerability and Pharmacokinetics of GSK2269557 Administered Via the ELLIPTA Dry Powder Inhaler to Healthy Subjects |
| NCT03073057 | PHASE1 | COMPLETED | Pharmacokinetic Study to Compare Absorption of Budesonide/Formoterol Easyhaler and Symbicort Turbuhaler |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).