Upadacitinib
FDA-approved product (tablet, extended release, oral), marketed as Rinvoq, Rinvoq Lq.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLNo approved indication recorded
ChEMBL records no approved indication for Upadacitinib. Its therapeutic class is shown instead.
- WHO therapeutic group
- Janus-associated kinase (jak) inhibitors
- FDA pharmacologic class
- Janus Kinase Inhibitor FDA label ↗
- Anti-infective classification
- Not classified as an anti-infective.
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against MRSA, E. coli and M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA52.4% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli41.8% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae37.2% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis54.5% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.
Evidence
Clinical and experimental
Documented evidenceClinical
50+registered studies name this medicine, for any condition. The registry search keeps the first 50, so there may be more. See them below.
Experimental
No evidence found
No laboratory measurement against the four pathogens in the ChEMBL records loaded here.
Docking
Computational · nothing measuredAutoDock Vina, one experimentally solved protein per pathogen. This project’s screening target is -7.0 kcal/mol, its own mark rather than a universal cutoff. A docking score is a structural hypothesis, not proof of binding, and requires experimental validation.
Other medicines to investigate
AI prediction · nothing measuredOther repurposing candidates: approved medicines besides Upadacitinib with AI-predicted activity ≥40% against the chosen pathogen, leaving out existing antimicrobials. They are computational candidates for further investigation, not alternatives and not recommendations.
Sorted by AI-predicted activity, high to low. The order is not a ranking of which medicine is better.
- DactinomycinExisting use: Kidney Wilms tumor, Neoplasm95.6% AI-predicted activityagainst MRSALab records exist50+ registered studies
- TaurursodiolExisting use: Bile acids and derivatives79.6% AI-predicted activityagainst MRSA43 registered studies
- LinaclotideExisting use: Constipation, Constipation disorder, Irritable bowel syndrome74.5% AI-predicted activityagainst MRSA50+ registered studies
- PlecanatideExisting use: Constipation74.4% AI-predicted activityagainst MRSA15 registered studies
- OxytocinExisting use: Hemorrhage, Uterine Inertia74.2% AI-predicted activityagainst MRSA50+ registered studies
- PosaconazoleExisting use: Aspergillosis, Candidiasis, Coccidioidomycosis and 2 more72.2% AI-predicted activityagainst MRSA50+ registered studies
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma70.6% AI-predicted activityagainst MRSA50+ registered studies
- TemsirolimusExisting use: Cancer, Clear cell renal carcinoma, Mantle cell lymphoma and 2 more70.1% AI-predicted activityagainst MRSA50+ registered studies
- Quizartinib DihydrochlorideExisting use: Acute myeloid leukemia, Myeloid leukemia70.0% AI-predicted activityagainst MRSA4 registered studies
- Irinotecan HydrochlorideExisting use: Adenocarcinoma, Cancer, Carcinoma and 4 more70.0% AI-predicted activityagainst MRSA50+ registered studies
- Deoxycholic AcidExisting use: Other dermatologicals69.3% AI-predicted activityagainst MRSA50+ registered studies
- ChenodiolExisting use: Cerebrotendinous xanthomatosis, Inborn errors of metabolism69.2% AI-predicted activityagainst MRSA30 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Active Pharmacovigilance Study of the Medicine Rinvoq™ (Upadacitinib)
NCT06498167 · start 2024-07-01
Registered record
- Registry ID
- NCT06498167
- Conditions
- Inflammatory Disease; Drug Side Effect; Drug Use; Adverse Drug Event; Adverse Drug Reaction; Safety Issues
- Interventions
- Upadacitinib
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2024-07-01
- Completion
- 2024-12-31
- Enrolment
- 150
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInflammatory Disease; Drug Side Effect; Drug Use; Adverse Drug Event +2 moreInterventionUpadacitinibPhaseNot recordedRegistry statusUnknownStudy of Oral Upadacitinib to Assess Change in Disease Activity and Adverse Events in Adult Participants With Ulcerative Colitis or Crohn's Disease
NCT06459297 · start 2024-06-24
Registered record
- Registry ID
- NCT06459297
- Conditions
- Ulcerative Colitis; Crohn's Disease
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2024-06-24
- Completion
- 2025-12-09
- Enrolment
- 105
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionUlcerative Colitis; Crohn's DiseaseInterventionNot recordedPhaseNot recordedRegistry statusCompletedAn Observational Study to Assess Real-World Use of Upadacitinib Tablets in Adolescent and Adult Participants With Moderate to Severe Atopic Dermatitis in China
NCT06421740 · start 2024-06-07
Registered record
- Registry ID
- NCT06421740
- Conditions
- Atopic Dermatitis
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2024-06-07
- Completion
- 2026-05-25
- Enrolment
- 1,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAtopic DermatitisInterventionNot recordedPhaseNot recordedRegistry statusCompletedDrug-Drug Interaction (DDI) Study of Leramistat in Healthy Adult Subjects
NCT06379958 · start 2024-04-08
Registered record
- Registry ID
- NCT06379958
- Conditions
- Pharmacokinetics
- Interventions
- leramistat 40mg; Itraconazole 200 mg; Phenytoin 100 Mg Oral Capsule; Simvastatin 40mg; Upadacitinib 15 MG
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Unknown
- Start
- 2024-04-08
- Completion
- 2024-09-30
- Enrolment
- 48
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPharmacokineticsInterventionleramistat 40mg; Itraconazole 200 mg; Phenytoin 100 Mg Oral Capsule; Simvastatin 40mg +1 morePhasePhase 1Registry statusUnknownIbd CAncer and seRious Infections in France (I-CARE 2)
NCT06089590 · start 2024-01-25
Registered record
- Registry ID
- NCT06089590
- Conditions
- IBD; Ulcerative Colitis; Crohn Disease
- Interventions
- Non-interventional
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2024-01-25
- Completion
- 2031-03-01
- Enrolment
- 6,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIBD; Ulcerative Colitis; Crohn DiseaseInterventionNon-interventionalPhaseNot recordedRegistry statusRecruitingUpadacitinib for Refractory Behcet's Syndrome
NCT07080346 · start 2024-01-25
Registered record
- Registry ID
- NCT07080346
- Conditions
- Behcet Syndrome
- Interventions
- Upadacitinib 15 MG
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2024-01-25
- Completion
- 2025-07-08
- Enrolment
- 27
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBehcet SyndromeInterventionUpadacitinib 15 MGPhasePhase 2Registry statusCompletedUpadacitinib Versus IL-17 Inhibitors in Patients With Psoriatic Arthritis
NCT07386717 · start 2024-01-01
Registered record
- Registry ID
- NCT07386717
- Conditions
- Psoriatic Arthritis; Upadacitinib; Interleukin-17 Inhibitors
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2024-01-01
- Completion
- 2025-12-31
- Enrolment
- 70
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsoriatic Arthritis; Upadacitinib; Interleukin-17 InhibitorsInterventionNot recordedPhaseNot recordedRegistry statusCompletedStudy to Assess Adverse Events, Change in Disease Activity, and How Oral Upadacitinib Moves Through the Body of Pediatric Participants With Moderately to Severely Active Ulcerative Colitis.
NCT05782907 · start 2023-11-06
Registered record
- Registry ID
- NCT05782907
- Conditions
- Ulcerative Colitis
- Interventions
- Upadacitinib
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Active not recruiting
- Start
- 2023-11-06
- Completion
- 2031-10
- Enrolment
- 122
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionUlcerative ColitisInterventionUpadacitinibPhasePhase 3Registry statusActive not recruitingReal World Study of Oral Upadacitinib Tablets to Assess Adverse Events and Change in Disease Activity in Adolescent and Adult Chinese Participants With Atopic Dermatitis
NCT05959083 · start 2023-08-18
Registered record
- Registry ID
- NCT05959083
- Conditions
- Atopic Dermatitis (AD)
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2023-08-18
- Completion
- 2026-05-07
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAtopic Dermatitis (AD)InterventionNot recordedPhaseNot recordedRegistry statusCompletedAn Observational Study to Assess Change in Disease Activity and Adverse Events in Adolescent and Adult Participants With Moderate to Severe Active Crohn's Disease (CD) in Japan
NCT06023030 · start 2023-07-28
Registered record
- Registry ID
- NCT06023030
- Conditions
- Crohn's Disease
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2023-07-28
- Completion
- 2027-05
- Enrolment
- 240
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCrohn's DiseaseInterventionNot recordedPhaseNot recordedRegistry statusRecruitingEfficacy and Safety of Low-Dose Upadacitinib Combined With Ustekinumab in the Treatment of Refractory Crohn's Disease
NCT07697547 · start 2023-07-01
Registered record
- Registry ID
- NCT07697547
- Conditions
- Inflammatory Bowel Disease (IBD); Crohn's Disease
- Interventions
- Upadacitinib; Ustekinumab (UST)
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2023-07-01
- Completion
- 2026-03-31
- Enrolment
- 84
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInflammatory Bowel Disease (IBD); Crohn's DiseaseInterventionUpadacitinib; Ustekinumab (UST)PhaseNot recordedRegistry statusCompletedStudy to Assess Change in Disease Activity and Adverse Events of Oral Upadacitinib Compared to Subcutaneous Adalimumab in Adult Participants With Moderate to Severe Rheumatoid Arthritis
NCT05814627 · start 2023-06-15
Registered record
- Registry ID
- NCT05814627
- Conditions
- Rheumatoid Arthritis
- Interventions
- Upadacitinib; Adalimumab; Upadacitinib Matching Placebo; Adalimumab Matching Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2023-06-15
- Completion
- 2026-07-15
- Enrolment
- 487
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRheumatoid ArthritisInterventionUpadacitinib; Adalimumab; Upadacitinib Matching Placebo; Adalimumab Matching PlaceboPhasePhase 3Registry statusCompletedNAZA - Nottingham/Astra ZenecA Prospective IBD Cohort Study
NCT06956703 · start 2022-12-12
Registered record
- Registry ID
- NCT06956703
- Conditions
- Gastro-Intestinal Disorder; Crohn Disease; Ulcerative Colitis; Inflammatory Bowel Diseases
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2022-12-12
- Completion
- 2027-12-31
- Enrolment
- 240
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGastro-Intestinal Disorder; Crohn Disease; Ulcerative Colitis; Inflammatory Bowel DiseasesInterventionNot recordedPhaseNot recordedRegistry statusRecruitingAn Observational Study to Assess Change in Disease Activity and Adverse Events of Upadacitinib in Adult Participants With Moderate to Severe Ulcerative Colitis (UC) in Real-World Practice
NCT05494606 · start 2022-08-15
Registered record
- Registry ID
- NCT05494606
- Conditions
- Ulcerative Colitis
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Active not recruiting
- Start
- 2022-08-15
- Completion
- 2028-03
- Enrolment
- 785
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionUlcerative ColitisInterventionNot recordedPhaseNot recordedRegistry statusActive not recruitingA Study to Assess Disease Activity in Adult Participants With Axial Spondyloarthritis Who Receive Upadacitinib in a Real-world Setting
NCT05094128 · start 2021-11-22
Registered record
- Registry ID
- NCT05094128
- Conditions
- Axial Spondylarthritis (r-axSpA)
- Interventions
- Upadacitinib
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Active not recruiting
- Start
- 2021-11-22
- Completion
- 2027-04
- Enrolment
- 338
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAxial Spondylarthritis (r-axSpA)InterventionUpadacitinibPhaseNot recordedRegistry statusActive not recruiting