Tadalafil
FDA-approved product (tablet, oral), marketed as Adcirca, Alyq, Chewtadzy and 3 more.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Benign prostatic hyperplasia
- Erectile dysfunction
- Impotence
- Pulmonary arterial hypertension
- Pulmonary hypertension
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Drugs used in erectile dysfunction
- FDA pharmacologic class
- Phosphodiesterase 5 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 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- MRSA50.8% 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. pneumoniae23.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis49.4% 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 measuredDihydrofolate 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 Tadalafil 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.
- Trimetrexate GlucuronateExisting use: Other agents against amoebiasis and other protozoal diseases88.6% AI-predicted activityagainst E. coliLab records exist17 registered studies
- Folic AcidExisting use: Acne, Anemia, Anemia (phenotype) and 8 more87.0% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- MethotrexateExisting use: Acute lymphoblastic leukemia, Adenoma, Arthritis and 21 more86.8% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- PralatrexateExisting use: Cancer, Mature T-cell and NK-cell non-Hodgkin lymphoma, Neoplasm and 2 more82.2% AI-predicted activityagainst E. coli44 registered studies
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives81.0% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- Leucovorin CalciumExisting use: Osteosarcoma67.6% AI-predicted activityagainst E. coli50+ registered studies
- LevoleucovorinExisting use: Anemia, Colorectal adenocarcinoma, Colorectal cancer and 3 more67.6% AI-predicted activityagainst E. coli50+ registered studies
- PyrimethamineExisting use: Malaria, Toxoplasmosis64.6% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- Copanlisib DihydrochlorideExisting use: Follicular lymphoma, Neoplasm, Neoplasm of mature B-cells63.5% AI-predicted activityagainst E. coli10 registered studies
- AfamelanotideExisting use: Erythropoietic protoporphyria62.6% AI-predicted activityagainst E. coli23 registered studies
- Rimegepant SulfateExisting use: Migraine disorder61.6% AI-predicted activityagainst E. coli50+ registered studies
- Histrelin AcetateExisting use: Neoplasm, Prostate adenocarcinoma, Prostate cancer61.6% AI-predicted activityagainst E. coli13 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Chemoimmunotherapy and Radiation in Pancreatic Cancer
NCT01903083 · start 2013-07
Registered record
- Registry ID
- NCT01903083
- Conditions
- Locally Advanced Malignant Neoplasm
- Interventions
- Tadalafil; Gemcitabine; Radiation; Pancreaticoduodenectomy
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2013-07
- Completion
- 2017-12
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLocally Advanced Malignant NeoplasmInterventionTadalafil; Gemcitabine; Radiation; PancreaticoduodenectomyPhasePhase 1Registry statusCompletedA Pharmacokinetics Study for Pediatric Participants With Pulmonary Arterial Hypertension
NCT01484431 · start 2012-07-17
Registered record
- Registry ID
- NCT01484431
- Conditions
- Pulmonary Arterial Hypertension
- Interventions
- Tadalafil- Tablet or Oral suspension
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Completed
- Start
- 2012-07-17
- Completion
- 2019-04-03
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonary Arterial HypertensionInterventionTadalafil- Tablet or Oral suspensionPhasePhase 1 / Phase 2Registry statusCompletedPhase 3 Study of Tadalafil Once-Daily in Asian Men With Benign Prostatic Hyperplasia (BPH)
NCT01460342 · start 2011-12
Registered record
- Registry ID
- NCT01460342
- Conditions
- Benign Prostatic Hyperplasia
- Interventions
- Tadalafil; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2011-12
- Completion
- 2012-10
- Enrolment
- 610
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBenign Prostatic HyperplasiaInterventionTadalafil; PlaceboPhasePhase 3Registry statusCompletedTadalafil and Sildenafil for Duchenne Muscular Dystrophy
NCT01359670 · start 2011-05
Registered record
- Registry ID
- NCT01359670
- Conditions
- Duchenne Muscular Dystrophy
- Interventions
- Tadalafil; Sildenafil
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Completed
- Start
- 2011-05
- Completion
- 2013-05
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDuchenne Muscular DystrophyInterventionTadalafil; SildenafilPhaseEarly phase 1Registry statusCompletedAortic Stenosis and PhosphodiEsterase iNhibition With Aortic Valve Replacement (ASPEN-AVR): A Pilot Study
NCT01272388 · start 2011-01
Registered record
- Registry ID
- NCT01272388
- Conditions
- Aortic Stenosis
- Interventions
- Tadalafil; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2011-01
- Completion
- 2012-04
- Enrolment
- 1
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAortic StenosisInterventionTadalafil; PlaceboPhasePhase 4Registry statusTerminatedA Study of First-Line Ambrisentan and Tadalafil Combination Therapy in Subjects With Pulmonary Arterial Hypertension (PAH)
NCT01178073 · start 2010-10-01
Registered record
- Registry ID
- NCT01178073
- Conditions
- Hypertension, Pulmonary
- Interventions
- ambrisentan; tadalafil
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2010-10-01
- Completion
- 2014-07-31
- Enrolment
- 610
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension, PulmonaryInterventionambrisentan; tadalafilPhasePhase 3Registry statusCompletedA Study of Tadalafil Use With Finasteride in Men With Enlarged Prostates and Urinary Symptoms
NCT01139762 · start 2010-09
Registered record
- Registry ID
- NCT01139762
- Conditions
- Benign Prostatic Hyperplasia; Enlarged Prostate
- Interventions
- Tadalafil; Placebo; Finasteride
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2010-09
- Completion
- 2012-05
- Enrolment
- 696
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBenign Prostatic Hyperplasia; Enlarged ProstateInterventionTadalafil; Placebo; FinasteridePhasePhase 3Registry statusCompletedA Study in Benign Prostatic Hyperplasia
NCT01152190 · start 2010-09
Registered record
- Registry ID
- NCT01152190
- Conditions
- Benign Prostatic Hyperplasia
- Interventions
- Tadalafil; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2010-09
- Completion
- 2012-07
- Enrolment
- 97
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBenign Prostatic HyperplasiaInterventionTadalafil; PlaceboPhasePhase 3Registry statusCompletedDo Phosphodiesterase 5A Inhibitors Improve Exercise Capacity in Patients With Chronic Obstructive Pulmonary Disease (COPD) and Pulmonary Hypertension?
NCT01197469 · start 2010-09
Registered record
- Registry ID
- NCT01197469
- Conditions
- Chronic Obstructive Pulmonary Disease; Pulmonary Hypertension
- Interventions
- Tadalafil; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2010-09
- Completion
- 2012-09
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Obstructive Pulmonary Disease; Pulmonary HypertensionInterventionTadalafil; PlaceboPhasePhase 2Registry statusCompletedTadalafil Effects in Left Ventricle Diastolic Dysfunction in Resistant Hypertensive Patients
NCT01743911 · start 2010-09
Registered record
- Registry ID
- NCT01743911
- Conditions
- Hypertension
- Interventions
- sugar pill; Tadalafil
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2010-09
- Completion
- 2012-08
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionsugar pill; TadalafilPhaseNot applicableRegistry statusCompletedA Study in Patients With Erectile Dysfunction
NCT01122264 · start 2010-05
Registered record
- Registry ID
- NCT01122264
- Conditions
- Erectile Dysfunction
- Interventions
- Tadalafil; Sildenafil Citrate
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2010-05
- Completion
- 2011-06
- Enrolment
- 770
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionErectile DysfunctionInterventionTadalafil; Sildenafil CitratePhasePhase 4Registry statusCompletedA Study to Determine if There is a Possible Association Between NAION and Phosphodiesterase Type 5 (PDE5) Inhibitors
NCT01131104 · start 2010-05
Registered record
- Registry ID
- NCT01131104
- Conditions
- Nonarteritic Anterior Ischemic Optic Neuropathy
- Interventions
- PDE5 Inhibitors
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2010-05
- Completion
- 2015-12
- Enrolment
- 345
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNonarteritic Anterior Ischemic Optic NeuropathyInterventionPDE5 InhibitorsPhaseNot recordedRegistry statusCompletedSildenafil to Tadalafil in Pulmonary Arterial Hypertension (SITAR)
NCT01043627 · start 2009-12
Registered record
- Registry ID
- NCT01043627
- Conditions
- Pulmonary Arterial Hypertension
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2009-12
- Completion
- 2011-12
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonary Arterial HypertensionInterventionNot recordedPhaseNot recordedRegistry statusCompletedA Randomized Control Trial to Assess the Efficacy of Tadalafil in Raynaud's Phenomenon in Scleroderma
NCT01117298 · start 2009-11
Registered record
- Registry ID
- NCT01117298
- Conditions
- Raynaud's Phenomenon; Digital Ulcers; Scleroderma
- Interventions
- Tadalafil; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2009-11
- Completion
- 2010-05
- Enrolment
- 66
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRaynaud's Phenomenon; Digital Ulcers; SclerodermaInterventionTadalafil; PlaceboPhasePhase 3Registry statusCompletedTadalafil in Treating Patients Undergoing Surgery for Cancer of the Oral Cavity or Oropharynx
NCT00843635 · start 2008-09
Registered record
- Registry ID
- NCT00843635
- Conditions
- Head and Neck Cancer
- Interventions
- Tadalafil; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2008-09
- Completion
- 2015-04
- Enrolment
- 35
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHead and Neck CancerInterventionTadalafil; PlaceboPhaseNot applicableRegistry statusCompleted