Disease Overview
Biomarker Targets & Therapeutic Agents
Gene targets queried against DGIdb, Open Targets, ChEMBL, PubMed, and Europe PMC. Agents ranked: Clinical > Mechanistic > Correlative.
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| SALVIANOLIC ACID B | ? unclear | Mechanistic | DGIdb | |
| CANDOXATRIL | ? unclear | Mechanistic | DGIdb | |
| CILAZAPRIL | ↓ inhibits | Mechanistic | DGIdb | |
| TP0556351 | ↓ inhibits | Mechanistic | DGIdb | |
| PRAVASTATIN SODIUM | ? unclear | Mechanistic | DGIdb | |
| SILDENAFIL | ? unclear | Mechanistic | DGIdb | |
| GEMFIBROZIL | ? unclear | Mechanistic | DGIdb | |
| RESCINNAMINE | ? unclear | Mechanistic | DGIdb | |
| SPIRAPRIL | ? unclear | Mechanistic | DGIdb | |
| INDOMETHACIN | ? unclear | Mechanistic | DGIdb | |
| HYDROCHLOROTHIAZIDE | ? unclear | Mechanistic | DGIdb | |
| ARGIPRESSIN | ? unclear | Mechanistic | DGIdb | |
| METOPROLOL | ? unclear | Mechanistic | DGIdb | |
| DELAPRIL | ↓ inhibits | Mechanistic | DGIdb | |
| ACETYLCHOLINE | ? unclear | Mechanistic | DGIdb | |
| THERAPEUTIC GLUCOCORTICOID | ? unclear | Mechanistic | DGIdb | |
| IMIDAPRIL | ↓ inhibits | Mechanistic | DGIdb | |
| MALATHION | ↓ inhibits | Mechanistic | DGIdb | |
| MOEXIPRIL | ? unclear | Mechanistic | 56.0 nM (IC50) | DGIdb |
| VORINOSTAT | ? unclear | Mechanistic | DGIdb | |
| ILEPATRIL | ↓ inhibits | Mechanistic | DGIdb | |
| RXP470.1 | ↓ inhibits | Mechanistic | DGIdb | |
| CGS-27023A | ? unclear | Mechanistic | DGIdb | |
| NITROPRUSSIDE | ? unclear | Mechanistic | DGIdb | |
| ENALAPRILAT ANHYDROUS | ↓ inhibits | Mechanistic | 1.2 nM (IC50) | DGIdb |
| TORSEMIDE | ? unclear | Mechanistic | DGIdb | |
| ATORVASTATIN CALCIUM TRIHYDRATE | ? unclear | Mechanistic | DGIdb | |
| FOSINOPRIL | ? unclear | Mechanistic | DGIdb | |
| FUROSEMIDE | ? unclear | Mechanistic | DGIdb | |
| TEMOCAPRIL HYDROCHLORIDE | ? unclear | Mechanistic | DGIdb | |
| BENAZEPRIL HYDROCHLORIDE | ↓ inhibits | Mechanistic | DGIdb | |
| CARBARIL | ↓ inhibits | Mechanistic | DGIdb | |
| BUPROPION HYDROCHLORIDE | ? unclear | Mechanistic | DGIdb | |
| QUINAPRIL | ? unclear | Mechanistic | 8.3 nM (IC50) | DGIdb |
| COMPOUND 1 [PMID: 24900526] | ↓ inhibits | Mechanistic | DGIdb | |
| COMPOUND 20 [PMID: 22153340] | ↓ inhibits | Mechanistic | DGIdb | |
| BUMETANIDE | ? unclear | Mechanistic | DGIdb | |
| GALLOPAMIL | ? unclear | Mechanistic | DGIdb | |
| FLUOXETINE HYDROCHLORIDE | ? unclear | Mechanistic | DGIdb | |
| AZD6605 | ↓ inhibits | Mechanistic | DGIdb |
Showing top 40 of 229 agents ranked by evidence tier.
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| ANTIVIRAL AGENT | ? unclear | Mechanistic | DGIdb | |
| IBALIZUMAB | ? unclear | Mechanistic | DGIdb | |
| CLENOLIXIMAB | ↓ inhibits | Mechanistic | DGIdb | |
| HERBIMYCIN | ? unclear | Mechanistic | DGIdb | |
| ZANOLIMUMAB | ? unclear | Mechanistic | DGIdb | |
| CEDELIZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| VRC-01LS | ~ modulates | Mechanistic | DGIdb | |
| TREGALIZUMAB | ↑ activates | Mechanistic | DGIdb | |
| PRILIXIMAB | ~ modulates | Mechanistic | DGIdb | |
| TRX1 | ? unclear | Mechanistic | DGIdb | |
| ANTISENSE OLIGONUCLEOTIDES | ? unclear | Mechanistic | DGIdb | |
| TRX-1 | ↓ inhibits | Mechanistic | DGIdb | |
| ANTI-THYMOCYTE GLOBULIN | ? unclear | Mechanistic | DGIdb | |
| SEMZUVOLIMAB | ↓ inhibits | Mechanistic | DGIdb | |
| KELIXIMAB | ~ modulates | Mechanistic | DGIdb | |
| ISOCOMPLESTATIN | ↓ inhibits | Mechanistic | 130.0 nM (IC50) | ChEMBL |
| CHLOROPEPTIN | ↓ inhibits | Mechanistic | 130.0 nM (IC50) | ChEMBL |
| CHEMBL3143464 | ↓ inhibits | Mechanistic | 130.0 nM (IC50) | ChEMBL |
| CHEMBL3138360 | ↑ activates | Mechanistic | 73000.0 nM (EC50) | ChEMBL |
| CHEMBL3138345 | ↑ activates | Mechanistic | 22000.0 nM (EC50) | ChEMBL |
| CHEMBL3138187 | ↑ activates | Mechanistic | 4000.0 nM (EC50) | ChEMBL |
| CHEMBL3138374 | ↑ activates | Mechanistic | 69600.0 nM (EC50) | ChEMBL |
| CHEMBL3138095 | ↑ activates | Mechanistic | 19900.0 nM (EC50) | ChEMBL |
| CHEMBL3138378 | ↑ activates | Mechanistic | 70400.0 nM (EC50) | ChEMBL |
| CHEMBL3138119 | ↑ activates | Mechanistic | 83800.0 nM (EC50) | ChEMBL |
| CHEMBL231224 | ↓ inhibits | Mechanistic | 80000.0 nM (Kd) | ChEMBL |
| CHEMBL267655 | ↓ inhibits | Mechanistic | 62000.0 nM (Kd) | ChEMBL |
| CHEMBL388209 | ↓ inhibits | Mechanistic | 20000.0 nM (Kd) | ChEMBL |
| CHEMBL230799 | ↓ inhibits | Mechanistic | 13000.0 nM (Kd) | ChEMBL |
| CHEMBL267658 | ↓ inhibits | Mechanistic | 26000.0 nM (Kd) | ChEMBL |
| CHEMBL388208 | ↓ inhibits | Mechanistic | 26000.0 nM (Kd) | ChEMBL |
| CHEMBL267657 | ↓ inhibits | Mechanistic | 16000.0 nM (Kd) | ChEMBL |
| CHEMBL230798 | ↓ inhibits | Mechanistic | 6000.0 nM (Kd) | ChEMBL |
| CHEMBL388207 | ↓ inhibits | Mechanistic | 27000.0 nM (Kd) | ChEMBL |
| CHEMBL230796 | ↓ inhibits | Mechanistic | 35000.0 nM (Kd) | ChEMBL |
| CHEMBL1852155 | ↓ inhibits | Mechanistic | 210.0 nM (IC50) | ChEMBL |
| CYCLOTRIAZADISULFONAMIDE HYDROCHLORIDE | ↓ inhibits | Mechanistic | 330.0 nM (IC50) | ChEMBL |
| CHEMBL4783030 | ↓ inhibits | Mechanistic | 2810.0 nM (IC50) | ChEMBL |
| CHEMBL4755141 | ↓ inhibits | Mechanistic | 860.0 nM (IC50) | ChEMBL |
| CHEMBL4783761 | ↓ inhibits | Mechanistic | 950.0 nM (IC50) | ChEMBL |
Showing top 40 of 52 agents ranked by evidence tier.
CYP27B1
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| TENOFOVIR DISOPROXIL FUMARATE | ? unclear | Mechanistic | DGIdb | |
| CHEMBL:CHEMBL2036072 | ? unclear | Mechanistic | DGIdb | |
| GAMMA-INTERFERON | ? unclear | Mechanistic | DGIdb | |
| DEFERASIROX | ? unclear | Mechanistic | DGIdb | |
| RIFAMPIN | ? unclear | Mechanistic | DGIdb | |
| TRICHOSTATIN A | ? unclear | Mechanistic | DGIdb | |
| DECITABINE | ? unclear | Mechanistic | DGIdb | |
| PEGINTERFERON ALFA-2A | ? unclear | Mechanistic | DGIdb | |
| SOY PROTEIN ISOLATE | ? unclear | Mechanistic | DGIdb | |
| CTA091 | ↓ inhibits | Mechanistic | DGIdb | |
| CHEMBL389014 | ↓ inhibits | Mechanistic | 554.0 nM (IC50) | ChEMBL |
| CHEMBL253613 | ↓ inhibits | Mechanistic | 616.0 nM (IC50) | ChEMBL |
| CHEMBL255088 | ↓ inhibits | Mechanistic | 554.0 nM (IC50) | ChEMBL |
| CHEMBL1170908 | ↓ inhibits | Mechanistic | 616.1 nM (IC50) | ChEMBL |
| CHEMBL4099180 | ↓ inhibits | Mechanistic | 60.2 nM (IC50) | ChEMBL |
| CHEMBL4081152 | ↓ inhibits | Mechanistic | 95.2 nM (IC50) | ChEMBL |
| CHEMBL4104395 | ↓ inhibits | Mechanistic | 570.0 nM (IC50) | ChEMBL |
| CHEMBL4074768 | ↓ inhibits | Mechanistic | 410.0 nM (IC50) | ChEMBL |
| KETOCONAZOLE | ↓ inhibits | Mechanistic | 340.0 nM (IC50) | ChEMBL |
IFNG
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| GANCICLOVIR | ? unclear | Mechanistic | DGIdb | |
| EMAPALUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| PEFLOXACIN | ? unclear | Mechanistic | DGIdb | |
| TRETINOIN | ? unclear | Mechanistic | DGIdb | |
| AMITRIPTYLINE HYDROCHLORIDE | ? unclear | Mechanistic | DGIdb | |
| MELPHALAN | ? unclear | Mechanistic | DGIdb | |
| CISPLATIN | ? unclear | Mechanistic | DGIdb | |
| EDRECOLOMAB | ? unclear | Mechanistic | DGIdb | |
| METHYLPREDNISOLONE | ? unclear | Mechanistic | DGIdb | |
| DOXIFLURIDINE | ? unclear | Mechanistic | DGIdb | |
| CYCLOPHOSPHAMIDE ANHYDROUS | ? unclear | Mechanistic | DGIdb | |
| URSODIOL | ? unclear | Mechanistic | DGIdb | |
| PREDNISONE | ? unclear | Mechanistic | DGIdb | |
| BLEOMYCIN | ? unclear | Mechanistic | DGIdb | |
| AMIKACIN | ? unclear | Mechanistic | DGIdb | |
| THERAPEUTIC GLUCOCORTICOID | ? unclear | Mechanistic | DGIdb | |
| FONTOLIZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| AMG-811 | ↓ inhibits | Mechanistic | DGIdb | |
| THEOPHYLLINE | ? unclear | Mechanistic | DGIdb | |
| PENICILLIN G POTASSIUM | ? unclear | Mechanistic | DGIdb | |
| TRASTUZUMAB | ? unclear | Mechanistic | DGIdb | |
| FUMARIC ACID | ? unclear | Mechanistic | DGIdb | |
| SURAMIN | ? unclear | Mechanistic | DGIdb | |
| IBUPROFEN, SODIUM SALT | ? unclear | Mechanistic | DGIdb | |
| THERAPEUTIC MELATONIN | ? unclear | Mechanistic | DGIdb | |
| THERAPEUTIC AUTOLOGOUS LYMPHOCYTES | ? unclear | Mechanistic | DGIdb | |
| THROMBIN ALFA | ? unclear | Mechanistic | DGIdb | |
| INTERFERON ALFA-2B | ? unclear | Mechanistic | DGIdb | |
| RECOMBINANT INTERLEUKIN-1-BETA | ? unclear | Mechanistic | DGIdb | |
| CHEMBL3288259 | ↓ inhibits | Mechanistic | 10000.0 nM (Kd) | ChEMBL |
| CHEMBL3288260 | ↓ inhibits | Mechanistic | 7000.0 nM (Kd) | ChEMBL |
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| NERELIMOMAB | ↓ inhibits | Mechanistic | DGIdb | |
| CROMOLYN SODIUM | ? unclear | Mechanistic | DGIdb | |
| PLACULUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| METHYLENE BLUE | ? unclear | Mechanistic | DGIdb | |
| ALTEPLASE | ? unclear | Mechanistic | DGIdb | |
| CARBOPLATIN | ? unclear | Mechanistic | DGIdb | |
| GENTAMICIN | ? unclear | Mechanistic | DGIdb | |
| GOLIMUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| BUPIVACAINE | ? unclear | Mechanistic | DGIdb | |
| PENTOXIFYLLINE | ? unclear | Mechanistic | 85000.0 nM (IC50) | DGIdb |
| BENZO[E]PYRENE | ? unclear | Mechanistic | DGIdb | |
| THALIDOMIDE | ? unclear | Mechanistic | DGIdb | |
| PYRAZINAMIDE | ? unclear | Mechanistic | DGIdb | |
| GLIMEPIRIDE | ? unclear | Mechanistic | DGIdb | |
| OMEPRAZOLE | ? unclear | Mechanistic | DGIdb | |
| LENERCEPT | ↓ inhibits | Mechanistic | DGIdb | |
| ADALIMUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| PRAZOSIN HYDROCHLORIDE | ? unclear | Mechanistic | DGIdb | |
| REMTOLUMAB | ? unclear | Mechanistic | DGIdb | |
| MIDOSTAURIN | ? unclear | Mechanistic | DGIdb | |
| LENABASUM | ? unclear | Mechanistic | DGIdb | |
| MAGNESIUM SULFATE ANHYDROUS | ? unclear | Mechanistic | DGIdb | |
| PICIBANIL | ? unclear | Mechanistic | DGIdb | |
| FLUOCINOLONE ACETONIDE | ? unclear | Mechanistic | DGIdb | |
| MILTEFOSINE | ? unclear | Mechanistic | DGIdb | |
| HOMIDIUM BROMIDE | ? unclear | Mechanistic | DGIdb | |
| OZORALIZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| PEGSUNERCEPT | ↓ inhibits | Mechanistic | DGIdb | |
| CERTOLIZUMAB PEGOL | ↓ inhibits | Mechanistic | DGIdb | |
| THERAPEUTIC HORMONE | ? unclear | Mechanistic | DGIdb | |
| NAFAMOSTAT | ? unclear | Mechanistic | DGIdb | |
| FOLIC ACID | ? unclear | Mechanistic | DGIdb | |
| ABBV-257 | ? unclear | Mechanistic | DGIdb | |
| RISPERIDONE | ? unclear | Mechanistic | DGIdb | |
| COVA322 | ? unclear | Mechanistic | DGIdb | |
| HYDROXYCHLOROQUINE | ? unclear | Mechanistic | DGIdb | |
| CERTOLIZUMAB | ? unclear | Mechanistic | DGIdb | |
| AN0128 | ? unclear | Mechanistic | DGIdb | |
| 5,7-DIHYDROXY-4-METHYLCOUMARIN | ? unclear | Mechanistic | DGIdb | |
| SORAFENIB | ? unclear | Mechanistic | DGIdb |
Showing top 40 of 277 agents ranked by evidence tier.
Clinical Trials
Drug, biologic and supplement trials (treatment or prevention) from ClinicalTrials.gov whose main condition is Sarcoidosis: recruiting, active or completed, most recently updated first. Data retrieved 2026-10-28.
This study will evaluate the clinical safety and efficacy of oral brepocitinib in participants with cutaneous sarcoidosis.
Open-label Study to Evaluate the Long-term Safety and Durability of Effect of XTMAB-16 in Patients With Pulmonary Sarcoidosis With or Without Extra-pulmonary Involvement
This is a Phase 2, randomized, double-blind, placebo-controlled, adaptive, multicenter study to evaluate the efficacy, safety, tolerability, Pharmacodynamics (PD), and Pharmacokinetics (PK) of OATD-01 in the treatment of subjects with active pulmonary sarcoidosis.
Study of Multiple-Ascending-Dose Study of XTMAB-16 in Patients with Pulmonary Sarcoidosis with or Without Extrapulmonary Manifestations
The purpose of this study is to investigate the role of the oral JAK1 inhibitor, abrocitinib 200 mg once daily, for the treatment of patients with moderate to severe cutaneous sarcoidosis.
Sarcoidosis is a systemic granulomatous disease of unknown aetiology, mainly affecting the lungs and lymphatics. It affects people worldwide (incidence, 4.7-64/100000; prevalence, 1-36/100000/year). Although it is most often a benign acute or subacute condition, sarcoidosis may progress to a disabli...
The primary objective of this study is to evaluate the effect of rilonacept, added to standard therapy and compared with standard therapy alone, on improvement in myocardial inflammation in subjects with cardiac sarcoidosis after 24 weeks of therapy.
Prospective randomized controlled trial comparing low dose Prednisone(or Prednisolone)/Methotrexate combination to standard dose Prednisone(or Prednisolone) in patients diagnosed with acute active clinically manifest cardiac sarcoidosis and not yet treated. The Investigators hypothesize that low dos...
This is a multicenter, randomized, double-blind, placebo-controlled, study comparing the efficacy and safety of intravenous (IV) efzofitimod 3 mg/kg and 5 mg/kg versus placebo after 48 weeks of treatment. This study will enroll adults with histologically confirmed pulmonary sarcoidosis receiving sta...
In severe refractory sarcoidosis not responding to conventional immunosuppressive treatment, the third-line tumor necrosis factor (TNF)-alpha inhibitor infliximab is an alternative. Treatment duration is not known, although it has been suggested that relapse rates after withdrawal could be high. We ...
The purpose of this study is to see if treatment with H.P. Acthar® Gel will result in the improvement and long-term stabilization of clinical and radiographic abnormalities that occur in patients with CNS sarcoidosis. In addition, it will also look at whether treatment will be also associated with i...
Sarcoidosis is an inflammatory condition affecting many different parts of the body but most commonly the lungs. It is not known what causes sarcoidosis. In some patients no treatment is needed but in other patients long term treatment may be required. One of the main medications used to manage this...
This study aims to evaluate the efficacy and safety of inhaled treprostinil in subjects with sarcoidosis-associated interstitial lung disease and pulmonary hypertension.
Sarcoidosis is a heterogeneous disorder of unknown etiology whose signature lesions are granulomatous inflammatory infiltrates in involved tissues. Tissue commonly affected are lungs, skin, eyes, lymph nodes and the heart. In this latter case, cardiac sarcoidosis (CS) can lead to atrioventricular (A...
The purpose of this proof of concept study was to determine whether CMK389 displays the safety and efficacy profile to support further development in chronic pulmonary sarcoidosis.
Agents Found By Disease-Level Search
Searched directly from “Sarcoidosis” via ClinicalTrials.gov interventions and Open Targets' disease→drug data — independent of the 5-gene target panel above. This surfaces agents whose mechanism doesn't route through a curated gene (combination therapies, standard-of-care drugs, targets outside the panel).
Not yet run. python -m biomarker_pipeline.run_disease_agent_discovery --disease "..."