Remission & chronicity
Biomarker Targets & Therapeutic Agents
Gene targets queried against DGIdb, Open Targets, ChEMBL, PubMed, and Europe PMC. Agents ranked: Clinical > Mechanistic > Correlative.
CTLA4
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| TREMELIMUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| IPILIMUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| CYCLOSPORINE | ? unclear | Mechanistic | DGIdb | |
| ATEZOLIZUMAB | ? unclear | Mechanistic | DGIdb | |
| VISILIZUMAB | ? unclear | Mechanistic | DGIdb | |
| BLEOMYCIN | ? unclear | Mechanistic | DGIdb | |
| ANTIBIOTIC | ? unclear | Mechanistic | DGIdb | |
| METHIMAZOLE | ? unclear | Mechanistic | DGIdb | |
| RETRO-INVERSO PEPTIDE | ? unclear | Mechanistic | DGIdb | |
| MELPHALAN | ? unclear | Mechanistic | DGIdb | |
| RECOMBINANT FAS LIGAND | ? unclear | Mechanistic | DGIdb | |
| ZALIFRELIMAB | ↓ inhibits | Mechanistic | DGIdb | |
| RIBAVIRIN | ? unclear | Mechanistic | DGIdb | |
| ANTI-THYMOCYTE GLOBULIN | ? unclear | Mechanistic | DGIdb | |
| QUAVONLIMAB | ↓ inhibits | Mechanistic | DGIdb | |
| COMPOUND 32 [PMID: 20471253] | ↓ inhibits | Mechanistic | DGIdb | |
| SIROLIMUS | ? unclear | Mechanistic | DGIdb | |
| BISPECIFIC ANTIBODY | ? unclear | Mechanistic | DGIdb | |
| CADONILIMAB | ↓ inhibits | Mechanistic | DGIdb | |
| APLITHIANINE A | ↓ inhibits | Mechanistic | DGIdb | |
| PEGINTERFERON ALFA-2A | ? unclear | Mechanistic | DGIdb | |
| INOSINE 5'-MONOPHOSPHATE DEHYDROGENASE INHIBITOR FF-10501-01 | ? unclear | Mechanistic | DGIdb | |
| ABATACEPT | ? unclear | Mechanistic | DGIdb | |
| WORTMANNIN | ? unclear | Mechanistic | DGIdb | |
| ERFONRILIMAB | ↓ inhibits | Mechanistic | DGIdb | |
| THALIDOMIDE | ? unclear | Mechanistic | DGIdb | |
| FF-10501-01 | ? unclear | Mechanistic | DGIdb | |
| PEGINTERFERON ALFA-2B | ? unclear | Mechanistic | DGIdb | |
| TETRADECANOYLPHORBOL ACETATE | ? unclear | Mechanistic | DGIdb | |
| DEHYDRATED ALCOHOL | ? unclear | Mechanistic | DGIdb | |
| PREDNISONE | ? unclear | Mechanistic | DGIdb | |
| CHEMBL5291170 | ↓ inhibits | Mechanistic | 31000.0 nM (Kd) | ChEMBL |
IL17A
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| SIMVASTATIN | ? unclear | Mechanistic | DGIdb | |
| IL-12 | ? unclear | Mechanistic | DGIdb | |
| SECUKINUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| TIBULIZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| BIMEKIZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| ANTI-IL17A MONOCLONAL ANTIBODY CJM112 | ? unclear | Mechanistic | DGIdb | |
| VUNAKIZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| M-1095 | ↓ inhibits | Mechanistic | DGIdb | |
| AFASEVIKUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| PERAKIZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| SIROLIMUS | ? unclear | Mechanistic | DGIdb | |
| GENTAMICIN | ? unclear | Mechanistic | DGIdb | |
| AZATHIOPRINE | ? unclear | Mechanistic | DGIdb | |
| VIDOFLUDIMUS | ? unclear | Mechanistic | DGIdb | |
| COVA322 | ? unclear | Mechanistic | DGIdb | |
| BRODALUMAB | ? unclear | Mechanistic | DGIdb | |
| IXEKIZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| IZOKIBEP | ↓ inhibits | Mechanistic | DGIdb | |
| REMTOLUMAB | ? unclear | Mechanistic | DGIdb | |
| TETRACYCLINE | ? unclear | Mechanistic | DGIdb | |
| ERYTHROMYCIN | ? unclear | Mechanistic | DGIdb | |
| MANNITOL | ? unclear | Mechanistic | DGIdb | |
| ABBV-257 | ? unclear | Mechanistic | DGIdb | |
| CJM-112 | ~ modulates | Mechanistic | DGIdb | |
| CHEMBL4872876 | ↓ inhibits | Mechanistic | 110.0 nM (Kd) | ChEMBL |
| CHEMBL4858175 | ↓ inhibits | Mechanistic | 12.3 nM (Kd) | ChEMBL |
| CHEMBL4854787 | ↓ inhibits | Mechanistic | 89.0 nM (Kd) | ChEMBL |
| CHEMBL4878993 | ↓ inhibits | Mechanistic | 12.9 nM (Kd) | ChEMBL |
| CHEMBL4869568 | ↓ inhibits | Mechanistic | 6.2 nM (Kd) | ChEMBL |
| CHEMBL4876088 | ↓ inhibits | Mechanistic | 10.1 nM (IC50) | ChEMBL |
| CHEMBL4860250 | ↓ inhibits | Mechanistic | 14.3 nM (IC50) | ChEMBL |
| CHEMBL4866932 | ↓ inhibits | Mechanistic | 10.1 nM (IC50) | ChEMBL |
| CHEMBL4874078 | ↓ inhibits | Mechanistic | 7.0 nM (IC50) | ChEMBL |
| CHEMBL4845695 | ↓ inhibits | Mechanistic | 2.8 nM (IC50) | ChEMBL |
| CHEMBL4855085 | ↓ inhibits | Mechanistic | 4.6 nM (IC50) | ChEMBL |
| CHEMBL4860574 | ↓ inhibits | Mechanistic | 2.0 nM (IC50) | ChEMBL |
| CHEMBL4865978 | ↓ inhibits | Mechanistic | 2.0 nM (IC50) | ChEMBL |
| CHEMBL4870813 | ↓ inhibits | Mechanistic | 1.0 nM (IC50) | ChEMBL |
| CHEMBL4850368 | ↓ inhibits | Mechanistic | 3.0 nM (IC50) | ChEMBL |
| CHEMBL4851738 | ↓ inhibits | Mechanistic | 3.0 nM (IC50) | ChEMBL |
Showing top 40 of 72 agents ranked by evidence tier.
IL23A
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| USTEKINUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| RISANKIZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| MIRIKIZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| BRAZIKUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| TILDRAKIZUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| GUSELKUMAB | ↓ inhibits | Mechanistic | DGIdb | |
| EBDAROKIMAB | ↓ inhibits | Mechanistic | DGIdb | |
| BRIAKINUMAB | ↓ inhibits | Mechanistic | DGIdb |
IL23R
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| INFLIXIMAB | ? unclear | Mechanistic | DGIdb | |
| AZATHIOPRINE | ? unclear | Mechanistic | DGIdb | |
| CELECOXIB | ? unclear | Mechanistic | DGIdb | |
| CHEMBL4206167 | ↓ inhibits | Mechanistic | 1.81 nM (Kd) | ChEMBL |
| CHEMBL4567228 | ↓ inhibits | Mechanistic | 113.0 nM (IC50) | ChEMBL |
| CHEMBL4555885 | ↓ inhibits | Mechanistic | 32.0 nM (IC50) | ChEMBL |
| CHEMBL4529484 | ↓ inhibits | Mechanistic | 25.0 nM (IC50) | ChEMBL |
| CHEMBL4577218 | ↓ inhibits | Mechanistic | 39.0 nM (IC50) | ChEMBL |
| CHEMBL4442232 | ↓ inhibits | Mechanistic | 892.0 nM (IC50) | ChEMBL |
| CHEMBL4565015 | ↓ inhibits | Mechanistic | 37.0 nM (IC50) | ChEMBL |
| CHEMBL4515769 | ↓ inhibits | Mechanistic | 199.0 nM (IC50) | ChEMBL |
| CHEMBL4451305 | ↓ inhibits | Mechanistic | 79.0 nM (IC50) | ChEMBL |
| CHEMBL4441983 | ↓ inhibits | Mechanistic | 220.0 nM (IC50) | ChEMBL |
| CHEMBL4537768 | ↓ inhibits | Mechanistic | 102.0 nM (IC50) | ChEMBL |
| CHEMBL4458363 | ↓ inhibits | Mechanistic | 78.0 nM (IC50) | ChEMBL |
| CHEMBL4454287 | ↓ inhibits | Mechanistic | 183.0 nM (IC50) | ChEMBL |
| CHEMBL4452903 | ↓ inhibits | Mechanistic | 57.0 nM (IC50) | ChEMBL |
| CHEMBL4457621 | ↓ inhibits | Mechanistic | 52.0 nM (IC50) | ChEMBL |
| CHEMBL4543753 | ↓ inhibits | Mechanistic | 518.0 nM (IC50) | ChEMBL |
| CHEMBL4527549 | ↓ inhibits | Mechanistic | 153.0 nM (IC50) | ChEMBL |
| CHEMBL4540496 | ↓ inhibits | Mechanistic | 223.0 nM (IC50) | ChEMBL |
| CHEMBL4524632 | ↓ inhibits | Mechanistic | 79.0 nM (IC50) | ChEMBL |
| CHEMBL4459265 | ↓ inhibits | Mechanistic | 124.0 nM (IC50) | ChEMBL |
| CHEMBL4550853 | ↓ inhibits | Mechanistic | 2584.0 nM (IC50) | ChEMBL |
| CHEMBL4435141 | ↓ inhibits | Mechanistic | 30000.0 nM (IC50) | ChEMBL |
| CHEMBL4446365 | ↓ inhibits | Mechanistic | 100.0 nM (IC50) | ChEMBL |
| CHEMBL4462185 | ↓ inhibits | Mechanistic | 96.0 nM (IC50) | ChEMBL |
| CHEMBL4454702 | ↓ inhibits | Mechanistic | 99.0 nM (IC50) | ChEMBL |
| CHEMBL4576008 | ↓ inhibits | Mechanistic | 95.0 nM (IC50) | ChEMBL |
| CHEMBL4589681 | ↓ inhibits | Mechanistic | 107.0 nM (IC50) | ChEMBL |
| CHEMBL4583420 | ↓ inhibits | Mechanistic | 101.0 nM (IC50) | ChEMBL |
| CHEMBL4440544 | ↓ inhibits | Mechanistic | 107.0 nM (IC50) | ChEMBL |
| CHEMBL4564118 | ↓ inhibits | Mechanistic | 47.0 nM (IC50) | ChEMBL |
| CHEMBL4537038 | ↓ inhibits | Mechanistic | 59.0 nM (IC50) | ChEMBL |
| CHEMBL4547985 | ↓ inhibits | Mechanistic | 206.0 nM (IC50) | ChEMBL |
| CHEMBL4558328 | ↓ inhibits | Mechanistic | 40.0 nM (IC50) | ChEMBL |
| CHEMBL4567670 | ↓ inhibits | Mechanistic | 139.0 nM (IC50) | ChEMBL |
| CHEMBL4582731 | ↓ inhibits | Mechanistic | 1885.0 nM (IC50) | ChEMBL |
| CHEMBL4435308 | ↓ inhibits | Mechanistic | 134.0 nM (IC50) | ChEMBL |
| CHEMBL4564607 | ↓ inhibits | Mechanistic | 48.0 nM (IC50) | ChEMBL |
Showing top 40 of 178 agents ranked by evidence tier.
JAK1
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| RUXOLITINIB | ↓ inhibits | Mechanistic | 3.0 nM (IC50) | DGIdb |
| IZENCITINIB | ↓ inhibits | Mechanistic | DGIdb | |
| PEMBROLIZUMAB | ? unclear | Mechanistic | DGIdb | |
| RUXOLITINIB PHOSPHATE | ↓ inhibits | Mechanistic | DGIdb | |
| GOLIDOCITINIB | ↓ inhibits | Mechanistic | DGIdb | |
| FILGOTINIB MALEATE | ↓ inhibits | Mechanistic | DGIdb | |
| MOMELOTINIB | ↓ inhibits | Mechanistic | 11.0 nM (IC50) | DGIdb |
| AZD1480 | ↓ inhibits | Mechanistic | DGIdb | |
| DELGOCITINIB | ↓ inhibits | Mechanistic | DGIdb | |
| TRICETAMIDE | ↓ inhibits | Mechanistic | DGIdb | |
| TOFACITINIB | ↓ inhibits | Mechanistic | 112.0 nM (IC50) | DGIdb |
| PEFICITINIB | ↓ inhibits | Mechanistic | DGIdb | |
| BREPOCITINIB | ↓ inhibits | Mechanistic | DGIdb | |
| UPADACITINIB HEMIHYDRATE | ↓ inhibits | Mechanistic | DGIdb | |
| CYCLOSPORINE | ? unclear | Mechanistic | DGIdb | |
| INCB-047986 | ↓ inhibits | Mechanistic | DGIdb | |
| ABROCITINIB | ↓ inhibits | Mechanistic | DGIdb | |
| ENZASTAURIN | ? unclear | Mechanistic | DGIdb | |
| CERDULATINIB | ↓ inhibits | Mechanistic | DGIdb | |
| NEZULCITINIB | ↓ inhibits | Mechanistic | DGIdb | |
| FILGOTINIB | ↓ inhibits | Mechanistic | DGIdb | |
| GLPG-0555 | ↓ inhibits | Mechanistic | DGIdb | |
| SOLCITINIB | ↓ inhibits | Mechanistic | DGIdb | |
| GUSACITINIB | ↓ inhibits | Mechanistic | DGIdb | |
| ITACITINIB | ↓ inhibits | Mechanistic | DGIdb | |
| BARICITINIB | ↓ inhibits | Mechanistic | DGIdb | |
| MOMELOTINIB DIHYDROCHLORIDE MONOHYDRATE | ? unclear | Mechanistic | Open Targets | |
| DEURUXOLITINIB PHOSPHATE | ? unclear | Mechanistic | Open Targets | |
| TOFACITINIB CITRATE | ? unclear | Mechanistic | Open Targets | |
| UPADACITINIB | ? unclear | Mechanistic | Open Targets | |
| CHEMBL538798 | ↓ inhibits | Mechanistic | 39810.72 nM (IC50) | ChEMBL |
| CHEMBL154580 | ↓ inhibits | Mechanistic | 19952.62 nM (IC50) | ChEMBL |
| SUNITINIB | ↓ inhibits | Mechanistic | 9.2 nM (Kd) | ChEMBL |
| CHEMBL386637 | ↓ inhibits | Mechanistic | 1300.0 nM (IC50) | ChEMBL |
| CHEMBL21156 | ↓ inhibits | Mechanistic | 15.0 nM (IC50) | ChEMBL |
| CHEMBL56543 | ↓ inhibits | Mechanistic | 3380.0 nM (IC50) | ChEMBL |
| DOVITINIB | ↓ inhibits | Mechanistic | 380.0 nM (Kd) | ChEMBL |
| JNJ-7706621 | ↓ inhibits | Mechanistic | 21.0 nM (Kd) | ChEMBL |
| SU-014813 | ↓ inhibits | Mechanistic | 97.0 nM (Kd) | ChEMBL |
| SOTRASTAURIN | ↓ inhibits | Mechanistic | 7300.0 nM (IC50) | ChEMBL |
Showing top 40 of 189 agents ranked by evidence tier.
PDE4D
| Therapeutic Agent | Effect Direction | Evidence Tier | Potency | Source |
|---|---|---|---|---|
| CILOMILAST | ↓ inhibits | Mechanistic | 63.0 nM (IC50) | DGIdb |
| TRANIMILAST | ↓ inhibits | Mechanistic | DGIdb | |
| RESVERATROL | ? unclear | Mechanistic | DGIdb | |
| DIFAMILAST | ↓ inhibits | Mechanistic | DGIdb | |
| MK-0873 | ↓ inhibits | Mechanistic | DGIdb | |
| REVAMILAST | ↓ inhibits | Mechanistic | DGIdb | |
| THEOPHYLLINE | ↓ inhibits | Mechanistic | DGIdb | |
| DYPHYLLINE | ↓ inhibits | Mechanistic | DGIdb | |
| IBUDILAST | ↓ inhibits | Mechanistic | DGIdb | |
| HT-0712 | ↓ inhibits | Mechanistic | DGIdb | |
| ENSIFENTRINE | ↓ inhibits | Mechanistic | DGIdb | |
| LIRIMILAST | ? unclear | Mechanistic | DGIdb | |
| OXTRIPHYLLINE | ↓ inhibits | Mechanistic | DGIdb | |
| DROTAVERIN | ↓ inhibits | Mechanistic | DGIdb | |
| TOFIMILAST | ↓ inhibits | Mechanistic | DGIdb | |
| THEOPHYLLINE SODIUM GLYCINATE | ↓ inhibits | Mechanistic | DGIdb | |
| DIPYRIDAMOLE | ↓ inhibits | Mechanistic | DGIdb | |
| GSK-356278 | ? unclear | Mechanistic | DGIdb | |
| APREMILAST | ↓ inhibits | Mechanistic | DGIdb | |
| ETAZOLATE | ? unclear | Mechanistic | DGIdb | |
| OGLEMILAST | ↓ inhibits | Mechanistic | DGIdb | |
| ZATOLMILAST | ↓ inhibits | Mechanistic | DGIdb | |
| TETOMILAST | ↓ inhibits | Mechanistic | DGIdb | |
| ROLIPRAM | ↓ inhibits | Mechanistic | 390.0 nM (IC50) | DGIdb |
| DENBUFYLLINE | ? unclear | Mechanistic | DGIdb | |
| LOTAMILAST | ↓ inhibits | Mechanistic | DGIdb | |
| PENTOXIFYLLINE | ↓ inhibits | Mechanistic | DGIdb | |
| AMLEXANOX | ↓ inhibits | Mechanistic | DGIdb | |
| AMINOPHYLLINE | ↓ inhibits | Mechanistic | DGIdb | |
| CRISABOROLE | ↓ inhibits | Mechanistic | DGIdb | |
| ROFLUMILAST | ↓ inhibits | Mechanistic | DGIdb | |
| PICLAMILAST | ? unclear | Mechanistic | 0.8 nM (IC50) | DGIdb |
| PAPAVERINE | ? unclear | Mechanistic | DGIdb | |
| GSK-256066 | ↓ inhibits | Mechanistic | DGIdb | |
| DIURETIC | ? unclear | Mechanistic | DGIdb | |
| BPN14770 | ? unclear | Mechanistic | DGIdb | |
| FLAVOXATE HYDROCHLORIDE | ↓ inhibits | Mechanistic | DGIdb | |
| SELECTIVE CYTOKINE INHIBITORY DRUG CC-1088 | ? unclear | Mechanistic | DGIdb | |
| DOVRAMILAST | ↓ inhibits | Mechanistic | DGIdb | |
| QUETIAPINE FUMARATE | ? unclear | Mechanistic | DGIdb |
Showing top 40 of 184 agents ranked by evidence tier.
| 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 Psoriatic Arthritis: recruiting, active or completed, most recently updated first. Data retrieved 2026-10-28.
The purpose of this study is to evaluate the safety and efficacy of risankizumab in adults with moderately to severely active psoriatic arthritis (PsA).
Researchers are looking for new ways to treat Psoriatic Arthritis (PsA). This study will help find out if a study medicine called tulisokibart (MK-7240) can treat symptoms of active PsA. This study assesses the efficacy, safety, and tolerability of tulisokibart in adult participants with active PsA....
The study will aim to estimate the efficacy of apremilast compared with placebo in the treatment of juvenile psoriatic arthritis (JPsA) in pediatric participants 5 to less than 18 years of age.
The purpose of this study is to evaluate the efficacy and safety of deucravacitinib versus placebo in participants with active psoriatic arthritis who are naïve to biologic disease-modifying anti-rheumatic drugs. The long term extension period will provide additional long-term efficacy and safety in...
Psoriatic arthritis (PsA) is a chronic inflammatory disease that affects the joints and skin in people who have psoriasis (PsO). The main aim of the study is to know how well zasocitinib (TAK-279) works in participants with active PsA who have not previously been treated with biologic disease-modify...
Psoriatic arthritis (PsA) is a chronic inflammatory disease that affects the joints and skin in people who have psoriasis (PsO). The main aim of the study is to know how well zasocitinib (TAK-279) works in participants with active PsA based on their previous experience with specific treatments. The ...
The purpose of this study is to determine the PK, safety and tolerability of multiple doses of intravenous (i.v.) secukinumab in pediatric participants with JPsA
The purpose of this Phase 2a/b study is: 1. to evaluate the efficacy, safety and tolerability of DDY391 in participants with psoriatic arthritis (PsA). 2. to determine the dose-response relationship of DDY391 in participants with PsA to support dose selection for Phase 3.
The purpose of this study is to evaluate the drug levels, efficacy, and safety of Deucravacitinib (BMS-986165) in pediatric participants with juvenile psoriatic arthritis.
This is a study to demonstrate the clinical efficacy, safety and tolerability of bimekizumab administered subcutaneously (sc) compared with placebo in the treatment of subjects with active Psoriatic Arthritis (PsA).
This is a study to demonstrate the clinical efficacy, safety and tolerability of bimekizumab administered subcutaneously (sc) compared with placebo in the treatment of tumor necrosis factor alpha-inadequate responders (TNFα-IR) subjects with active Psoriatic Arthritis (PsA).
The main purpose of this study is to assess the effectiveness of adding tirzepatide to ixekizumab therapy in standard clinical practice in participants with active PsA and obesity or overweight with at least 1 weight-related comorbidity. The study will last up to 12 months.
The purpose of this study is to evaluate the safety and efficacy of deucravacitinib versus placebo for the treatment of participants with active PsA who are naïve to biologic disease modifying antirheumatic drugs or had previously received TNFα inhibitor treatment.The long term extension period will...
Psoriatic arthritis (PsA) is a long-term inflammatory disease that affects the joints and skin. The purpose of this study is to check how safe zasocitinib is, how well it is tolerated and how well it works in adults with PsA over a longer period of time. Adults who completed the 1-year (52-week) tre...
This is a study to assess the long-term safety, long-term efficacy and tolerability of bimekizumab administered subcutaneously (sc) in adult subjects with psoriatic arthritis (PsA).
Agents Found By Disease-Level Search
Searched directly from “Psoriatic Arthritis” via ClinicalTrials.gov interventions and Open Targets' disease→drug data — independent of the 7-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).
48 agents shown (approved or with trial evidence) — 35 not found by the gene-target search above.
Secukinumab
Adalimumab
MethotrexateNOT in gene-target list
Guselkumab
Bimekizumab
Etanercept
Risankizumab
Ixekizumab
Ustekinumab
DeucravacitinibNOT in gene-target list
Apremilast
golimumab
ZasocitinibNOT in gene-target list
IL-17iNOT in gene-target list
secukinumab (AIN457A)NOT in gene-target list
CabozantinibNOT in gene-target list
FluoropyrimidineNOT in gene-target list
Ipilimumab
NivolumabNOT in gene-target list
Platinum CompoundNOT in gene-target list
Platinum DoubletNOT in gene-target list
Baricitinib
LeucovorinNOT in gene-target list
deucravacitinib (BMS-986165)NOT in gene-target list
Ustekinumab 45 mg - CPNOT in gene-target list
Placebo to ustekinumab 45 mg - after CPNOT in gene-target list
Ustekinumab 45 mg - after CPNOT in gene-target list
Secukinumab and PlaceboNOT in gene-target list
Routine practice groupNOT in gene-target list
EARP groupNOT in gene-target list
Employment and Arthritis: Making it WorkNOT in gene-target list
Pharmacokinetics of certolizumab pegolNOT in gene-target list
BMS-986165 Dose ANOT in gene-target list
BMS-986165 Dose BNOT in gene-target list
OCTA-SCPNOT in gene-target list
OCTA-DCPNOT in gene-target list
OCTA-RPCNOT in gene-target list
OCTA-FAZNOT in gene-target list
Single nucleotide polymorphisms (SNP)NOT in gene-target list
3'mRNA sequencingNOT in gene-target list
Enzyme-linked immunosorbent assay (ELISA) and Legendplex ArrayNOT in gene-target list
Flow CytometryNOT in gene-target list
Serum vitaminDlevelNOT in gene-target list
MetforminNOT in gene-target list
Upadacitinib
Placebo to UpadacitinibNOT in gene-target list
Placebo to AdalimumabNOT in gene-target list
Guselkumab 100 mgNOT in gene-target list
Generated by the Open Source Medicine Foundation Biomarker Pipeline — 2026-10-08. Data sources: DGIdb, Open Targets, ChEMBL, PubMed, ClinicalTrials.gov. Not medical advice.