Prednisone
FDA-approved product (tablet, oral), marketed as Cortan, Delta-Dome, Deltasone and 10 more.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 1 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Adrenal gland disease
- Allergic conjunctivitis
- Allergic rhinitis
- Anemia
- Ankylosing spondylitis
- Aplastic anemia
- Arthritis
- Asthma
- Atopic eczema
- Autoimmune thrombocytopenic purpura
- Berylliosis
- Brain neoplasm
- Bursitis
- Cancer
- Chorioretinitis
- Choroiditis
- and 60 more
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Corticosteroids for local oral treatment; Corticosteroids acting locally; Corticosteroids; Corticosteroids, weak (group i); Corticosteroids, weak, other combinations
- FDA pharmacologic class
- Corticosteroid 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. It was surfaced computationally for further investigation; it is not an established treatment for this infection.
AI-predicted activity
AI prediction · nothing measured- MRSA46.4% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli30.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae17.7% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis35.2% AI-predicted activityBelow 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 measuredDihydrofolate reductase ↗ (E. coli)
Not yet docked: queued in the docking rundetails
KPC-2 carbapenemase ↗ (K. pneumoniae)
Not yet docked: queued in the docking rundetails
Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)
Not yet docked: queued in the docking rundetails
Dihydrofolate reductase ↗ (MRSA)
Not yet docked: queued in the docking rundetails
AutoDock 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 Prednisone 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.
- FurazolidoneExisting use: Other antiinfectives and antiseptics91.4% AI-predicted activityagainst M. tuberculosisLab records exist49 registered studies
- TriflupromazineExisting use: Psychosis90.6% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- ValdecoxibExisting use: Dysmenorrhea, Osteoarthritis, Rheumatic disease and 1 more88.6% AI-predicted activityagainst M. tuberculosisLab records exist31 registered studies
- CelecoxibExisting use: Ankylosing spondylitis, Cancer, Colorectal neoplasm and 15 more87.6% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Dorzolamide HydrochlorideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma86.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- MethazolamideExisting use: Glaucoma, Open-angle glaucoma85.6% AI-predicted activityagainst M. tuberculosisLab records exist11 registered studies
- AcetazolamideExisting use: Altitude sickness, Angle-closure glaucoma, Congestive heart failure and 5 more85.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Trifluoperazine HydrochlorideExisting use: Anxiety disorder, Mental or behavioural disorder, Psychosis and 1 more84.6% AI-predicted activityagainst M. tuberculosis1 registered study
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives84.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- NitrofurazoneExisting use: Eye infection, Leishmaniasis, Trypanosomiasis84.0% AI-predicted activityagainst M. tuberculosis8 registered studies
- BrinzolamideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma83.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- ZonisamideExisting use: Epilepsy, Focal-onset seizure, Partial epilepsy and 1 more82.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Phase II Randomized Trial of Radiation Therapy in Oligometastatic mCRPC Prostate Cancer (ARTO)
NCT03449719 · start 2018-05-01
Registered record
- Registry ID
- NCT03449719
- Conditions
- Rate of PSA Response in Oligometastatic,CRPC Undergoing SBRT in Combination With Abiraterone Acetate (AA), Compared to Patients Treated With AA Alone
- Interventions
- SBRT - Ablative radiation Therapy; Abiraterone Acetate
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2018-05-01
- Completion
- 2022-05-01
- Enrolment
- 174
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRate of PSA Response in Oligometastatic,CRPC Undergoing SBRT in Combination With Abiraterone Acetate (AA), Compared to Patients Treated With AA AloneInterventionSBRT - Ablative radiation Therapy; Abiraterone AcetatePhaseNot applicableRegistry statusUnknownDexamethasone Versus Prednisone for Asthma Treatment in the Pediatric Inpatient Population; a Feasibility Study
NCT03133897 · start 2018-03-05
Registered record
- Registry ID
- NCT03133897
- Conditions
- Asthma
- Interventions
- Dexamethasone; Prednisone
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Terminated
- Start
- 2018-03-05
- Completion
- 2020-03-11
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAsthmaInterventionDexamethasone; PrednisonePhasePhase 3Registry statusTerminatedThalidomide Combined With R-CHOP in Newly Diagnosed,Untreated Double-expressor Diffuse Large B-Cell Lymphoma Patients
NCT03318835 · start 2017-08-22
Registered record
- Registry ID
- NCT03318835
- Conditions
- Thalidomide
- Interventions
- Thalidomide combined with R-CHOP; R-CHOP
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2017-08-22
- Completion
- 2020-08-22
- Enrolment
- 162
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionThalidomideInterventionThalidomide combined with R-CHOP; R-CHOPPhasePhase 3Registry statusUnknownSafety and Efficacy of Blinatumomab in Adults With Newly Diagnosed High-risk Diffuse Large B-Cell Lymphoma
NCT03023878 · start 2017-03-13
Registered record
- Registry ID
- NCT03023878
- Conditions
- High-risk Diffuse Large B-Cell Lymphoma
- Interventions
- Blinatumomab; Investigator's Choice Chemotherapy; Dexamethasone
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2017-03-13
- Completion
- 2019-10-28
- Enrolment
- 47
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHigh-risk Diffuse Large B-Cell LymphomaInterventionBlinatumomab; Investigator's Choice Chemotherapy; DexamethasonePhasePhase 2Registry statusCompletedCinobufacini Tablets Combined With Chemotherapeutic Protocol in Treatment of Diffuse Large B Cell Lymphoma
NCT02871869 · start 2016-09
Registered record
- Registry ID
- NCT02871869
- Conditions
- Diffuse, Large B-Cell, Lymphoma
- Interventions
- vindesine; cyclophosphamide; Epirubicin; prednisone tablets; Cinobufacini Tablets; Rituximab
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Unknown
- Start
- 2016-09
- Completion
- 2021-12
- Enrolment
- 316
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiffuse, Large B-Cell, LymphomaInterventionvindesine; cyclophosphamide; Epirubicin; prednisone tablets +2 morePhasePhase 2 / Phase 3Registry statusUnknownThe Efficacy of TCD Following by TP Maintenance Therapy in Newly Diagnosed WM
NCT02844309 · start 2016-05
Registered record
- Registry ID
- NCT02844309
- Conditions
- Waldenström Macroglobulinemia
- Interventions
- Thalidomide
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2016-05
- Completion
- 2020-05
- Enrolment
- 44
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionWaldenström MacroglobulinemiaInterventionThalidomidePhasePhase 4Registry statusCompletedCorticosteroids With Vedolizumab in Crohn's Disease
NCT02324699 · start 2016-04
Registered record
- Registry ID
- NCT02324699
- Conditions
- Crohn's Disease
- Interventions
- Prednisone; Placebo; Vedolizumab
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2016-04
- Completion
- 2018-02-08
- Enrolment
- 1
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCrohn's DiseaseInterventionPrednisone; Placebo; VedolizumabPhasePhase 4Registry statusTerminatedInitiation of a Deceased Donor Uterine Transplantation Program at the University of Nebraska Medical Center
NCT02409147 · start 2016-01
Registered record
- Registry ID
- NCT02409147
- Conditions
- Uterus Transplant
- Interventions
- Uterine Transplant
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Withdrawn
- Start
- 2016-01
- Completion
- 2018-07-24
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionUterus TransplantInterventionUterine TransplantPhaseNot applicableRegistry statusWithdrawnRepeat Emergency Department Visits Among Patients With Asthma and COPD
NCT02499887 · start 2016-01
Registered record
- Registry ID
- NCT02499887
- Conditions
- Asthma; COPD
- Interventions
- beclamethasone dipropionate; albuterol; Prednisone
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Terminated
- Start
- 2016-01
- Completion
- 2016-09
- Enrolment
- 6
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAsthma; COPDInterventionbeclamethasone dipropionate; albuterol; PrednisonePhaseNot applicableRegistry statusTerminatedTreatment for Classical Hodgkin Lymphoma in Children and Adolescents
NCT02797717 · start 2015-11
Registered record
- Registry ID
- NCT02797717
- Conditions
- Classical Hodgkins Lymphoma in Children and Adolescents.
- Interventions
- Radiotherapy:; Vincristine; Etoposide; Prednisone; Doxorubicin; Dacarbazine; Cyclophosphamide
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2015-11
- Completion
- 2027-12
- Enrolment
- 2,200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionClassical Hodgkins Lymphoma in Children and Adolescents.InterventionRadiotherapy:; Vincristine; Etoposide; Prednisone +3 morePhaseNot applicableRegistry statusRecruitingGlucocorticoid in Treatment of Adult Idiopathic Nephrotic Syndrome:a Prospective Observational Study
NCT02298335 · start 2014-05-13
Registered record
- Registry ID
- NCT02298335
- Conditions
- Nephrotic Syndrome,Idiopathic
- Interventions
- prednisone
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2014-05-13
- Completion
- 2020-10-22
- Enrolment
- 235
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNephrotic Syndrome,IdiopathicInterventionprednisonePhaseNot applicableRegistry statusCompletedTreatment With a Scheme With Low Doses of Bortezomib / Melphalan / Prednisone (MPV) in Patients With Multiple Myeloma
NCT02773550 · start 2014-01
Registered record
- Registry ID
- NCT02773550
- Conditions
- Multiple Myeloma
- Interventions
- Bortezomib; Melphalan; Prednisone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2014-01
- Completion
- 2018-07
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMultiple MyelomaInterventionBortezomib; Melphalan; PrednisonePhasePhase 4Registry statusTerminatedShort-term Prednisone to Treat STA Study(SPTSS)
NCT01837433 · start 2013-03
Registered record
- Registry ID
- NCT01837433
- Conditions
- Subacute Thyroiditis
- Interventions
- Prednisone 1 week; Prednisone 6 weeks
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2013-03
- Completion
- 2014-12
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSubacute ThyroiditisInterventionPrednisone 1 week; Prednisone 6 weeksPhasePhase 4Registry statusCompletedPostoperative Systemic Corticosteroids When Utilizing a Steroid-Eluting Spacer Following Endoscopic Sinus Surgery
NCT01564355 · start 2012-04
Registered record
- Registry ID
- NCT01564355
- Conditions
- Chronic Sinusitis; Endoscopic Sinus Surgery; Post-operative Care; Steroids; Drug-eluting Spacer
- Interventions
- Steroid-eluting middle meatal spacer (Nasopore (TM) spacer impregnated with 1 cc of 40mg/mL triamcinolone liquid); Post-op Oral Steroids
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2012-04
- Completion
- 2013-12
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Sinusitis; Endoscopic Sinus Surgery; Post-operative Care; Steroids +1 moreInterventionSteroid-eluting middle meatal spacer (Nasopore (TM) spacer impregnated with 1 cc of 40mg/mL triamcinolone liquid); Post-op Oral SteroidsPhaseNot applicableRegistry statusCompletedThe Efficacy of Prednisone and Azithromycin in the Treatment of Patients With Cat Scratch Disease
NCT01469702 · start 2011-12
Registered record
- Registry ID
- NCT01469702
- Conditions
- Cat-scratch Disease; Bartonella Infections
- Interventions
- prednison and azithromycin; prednison, azithromycin; prednison, Azenil
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2011-12
- Completion
- Not recorded
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCat-scratch Disease; Bartonella InfectionsInterventionprednison and azithromycin; prednison, azithromycin; prednison, AzenilPhasePhase 4Registry statusUnknown