Apremilast
FDA-approved product (tablet, oral), marketed as Apremilast, Otezla, Otezla Xr.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 1 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Behcet's syndrome
- Immune system disease
- Oral ulcer
- Psoriasis
- Psoriasis vulgaris
- Psoriatic arthritis
- Pustulosis palmaris et plantaris
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Selective immunosuppressants
- FDA pharmacologic class
- Phosphodiesterase 4 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 M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for this infection.
AI-predicted activity
AI prediction · nothing measured- MRSA36.5% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli35.5% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae26.1% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis60.0% 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 Apremilast 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.
Utilization of a Microdevice for Psoriasis and Atopic Dermatitis
NCT07352566 · start 2026-08-01
Registered record
- Registry ID
- NCT07352566
- Conditions
- Psoriasis; Atopic Dermatitis
- Interventions
- In situ cutaneous microdevice; Triamcinolone; 5-Fluorouracil; Calcipotriene; Tapinarof; Crisaborole; Tacrolimus; Adalimumab; Etanercept; Certolizumab; Infliximab; Secukinumab; Ixekizumab; Apremilast; Risankizumab; Ustekinumab; Hydroxychloroquine; Methotrexate; Mycophenolate; Azathioprine; Chloroquine; Cyclosporine; Tofacitinib; Deucravacitinib; Dupilumab; Tralokinumab; Guselkumab; Tildrakizumab; Baractinib; Abrocitinib; Upadacitinib; Lebrikizumab; Nemolizumab; Ruxolitinib; Bimekizumab; Roflumilast
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Not yet recruiting
- Start
- 2026-08-01
- Completion
- 2030-06-01
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsoriasis; Atopic DermatitisInterventionIn situ cutaneous microdevice; Triamcinolone; 5-Fluorouracil; Calcipotriene +32 morePhasePhase 4Registry statusNot yet recruitingEFFICACY OF ROFLUMILAST IN THE TREATMENT OF FLEXURAL AND/OR GENITAL PSORIASIS: A RANDOMIZED CONTROLLED TRIAL.
NCT07543640 · start 2026-04-01
Registered record
- Registry ID
- NCT07543640
- Conditions
- Flexural Psoriasis (Also Known as Inverse or Intertriginous Psoriasis) and Genital Psoriasis
- Interventions
- Methotrexate; Roflumilast 500 Mcg Oral Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-04-01
- Completion
- 2026-08
- Enrolment
- 56
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionFlexural Psoriasis (Also Known as Inverse or Intertriginous Psoriasis) and Genital PsoriasisInterventionMethotrexate; Roflumilast 500 Mcg Oral TabletPhasePhase 2Registry statusNot yet recruitingEffect of Anti-Psoriatic Biologics on Risk of Anogenital Warts (CONDYPSO)
NCT07234838 · start 2026-02-01
Registered record
- Registry ID
- NCT07234838
- Conditions
- Psoriasis; Condyloma Acuminata; Biotherapies
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2026-02-01
- Completion
- 2028-08-01
- Enrolment
- 600
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsoriasis; Condyloma Acuminata; BiotherapiesInterventionNot recordedPhaseNot recordedRegistry statusRecruitingPhase 4 Multicenter, Open-label Study on Efficacy and Safety of Apremilast in Moderate-to-severe Psoriasis
NCT07190391 · start 2025-09-30
Registered record
- Registry ID
- NCT07190391
- Conditions
- Psoriasis
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Not yet recruiting
- Start
- 2025-09-30
- Completion
- 2027-10-31
- Enrolment
- 425
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsoriasisInterventionNot recordedPhaseNot recordedRegistry statusNot yet recruitingUstekinumab in BEhçet's Syndrome STudy
NCT07244614 · start 2025-09-01
Registered record
- Registry ID
- NCT07244614
- Conditions
- Behçet's Syndrome (BS)
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2025-09-01
- Completion
- 2029-12-31
- Enrolment
- 208
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBehçet's Syndrome (BS)InterventionNot recordedPhaseNot recordedRegistry statusRecruitingComparison of Otezla to SFA-002 to Placebo in Plaque Psoriasis Patients
NCT06863493 · start 2025-06-01
Registered record
- Registry ID
- NCT06863493
- Conditions
- Psoriasis (PsO)
- Interventions
- SFA002; Otezla; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Not yet recruiting
- Start
- 2025-06-01
- Completion
- 2026-09-01
- Enrolment
- 125
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsoriasis (PsO)InterventionSFA002; Otezla; PlaceboPhasePhase 2 / Phase 3Registry statusNot yet recruitingHPP737 in Adult Patients With Plaque Psoriasis
NCT07712731 · start 2025-04-18
Registered record
- Registry ID
- NCT07712731
- Conditions
- Psoriasis
- Interventions
- HPP737; Placebo matching HPP737; Apremilast; Placebo matching Apremilast
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2025-04-18
- Completion
- 2026-04-01
- Enrolment
- 607
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsoriasisInterventionHPP737; Placebo matching HPP737; Apremilast; Placebo matching ApremilastPhasePhase 3Registry statusCompletedApremilast for Alcohol Use Disorder Treatment in Women and Men
NCT06324435 · start 2024-05-08
Registered record
- Registry ID
- NCT06324435
- Conditions
- Alcohol Use Disorder
- Interventions
- Apremilast
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Active not recruiting
- Start
- 2024-05-08
- Completion
- 2026-08-30
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAlcohol Use DisorderInterventionApremilastPhasePhase 1Registry statusActive not recruitingA Study About How Well TAK-279 Works and Its Safety in Participants With Moderate-to-severe Plaque Psoriasis During 52 Weeks of Treatment
NCT06088043 · start 2023-11-06
Registered record
- Registry ID
- NCT06088043
- Conditions
- Plaque Psoriasis
- Interventions
- TAK-279; Placebo; Apremilast
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2023-11-06
- Completion
- 2025-10-22
- Enrolment
- 693
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPlaque PsoriasisInterventionTAK-279; Placebo; ApremilastPhasePhase 3Registry statusCompletedA Study About How Well TAK-279 Works and Its Safety in Participants With Moderate-to-severe Plaque Psoriasis During 60 Weeks of Treatment With a Withdrawal and Retreatment Period
NCT06108544 · start 2023-11-06
Registered record
- Registry ID
- NCT06108544
- Conditions
- Plaque Psoriasis
- Interventions
- TAK-279; Placebo; Apremilast
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2023-11-06
- Completion
- 2025-11-07
- Enrolment
- 1,108
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPlaque PsoriasisInterventionTAK-279; Placebo; ApremilastPhasePhase 3Registry statusCompletedA Study of Apremilast in Pediatric Participants in Children With Mild to Moderate Plaque Psoriasis
NCT06088199 · start 2023-10-24
Registered record
- Registry ID
- NCT06088199
- Conditions
- Plaque Psoriasis
- Interventions
- Apremilast
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2023-10-24
- Completion
- 2026-08-12
- Enrolment
- 51
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPlaque PsoriasisInterventionApremilastPhasePhase 3Registry statusCompleted[18F]PF-06445974 to Image PDE4B in Major Depressive Disorder Using PET
NCT05703685 · start 2023-06-22
Registered record
- Registry ID
- NCT05703685
- Conditions
- Depression
- Interventions
- Lung scan; Apremilast; 18F-PF-06445974
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Recruiting
- Start
- 2023-06-22
- Completion
- 2029-04-11
- Enrolment
- 108
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDepressionInterventionLung scan; Apremilast; 18F-PF-06445974PhasePhase 1Registry statusRecruitingA Study to Assess the Efficacy and Safety of Apremilast in Japanese Pediatric Participants With Moderate to Severe Plaque Psoriasis
NCT05565560 · start 2023-01-25
Registered record
- Registry ID
- NCT05565560
- Conditions
- Plaque Psoriasis
- Interventions
- Apremilast
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Active not recruiting
- Start
- 2023-01-25
- Completion
- 2026-09-03
- Enrolment
- 17
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPlaque PsoriasisInterventionApremilastPhasePhase 3Registry statusActive not recruitingRandomized Double Blind Controlled Trial Comparing the Safety and Efficacy of Apremilast Versus Placebo in Severe Forms of Recurrent Aphthous Stomatitis
NCT04227314 · start 2022-04-10
Registered record
- Registry ID
- NCT04227314
- Conditions
- Recurrent Aphtous Stomatitis
- Interventions
- Apremilast; Placebo oral tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2022-04-10
- Completion
- 2026-12
- Enrolment
- 134
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRecurrent Aphtous StomatitisInterventionApremilast; Placebo oral tabletPhasePhase 3Registry statusRecruitingApremilast Pediatric Study in Children With Active Juvenile Psoriatic Arthritis
NCT04804553 · start 2022-03-17
Registered record
- Registry ID
- NCT04804553
- Conditions
- Active Juvenile Psoriatic Arthritis
- Interventions
- Apremilast; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2022-03-17
- Completion
- 2028-12-29
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionActive Juvenile Psoriatic ArthritisInterventionApremilast; PlaceboPhasePhase 3Registry statusRecruiting