Riociguat
FDA-approved product (tablet, oral), marketed as Adempas, Riociguat.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Hypertension
- Idiopathic and/or familial pulmonary arterial hypertension
- Pulmonary arterial hypertension
- Pulmonary hypertension
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Antihypertensives for pulmonary arterial hypertension
- FDA pharmacologic class
- Soluble Guanylate Cyclase Stimulator 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- MRSA46.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli32.5% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae28.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis68.0% 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 Riociguat 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.
- Ozanimod HydrochlorideExisting use: Multiple sclerosis, Relapsing-remitting multiple sclerosis, Ulcerative colitis66.8% AI-predicted activityagainst MRSA7 registered studies
- Micafungin SodiumExisting use: Candidiasis66.8% AI-predicted activityagainst MRSA50+ registered studies
- AbemaciclibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 3 more66.4% AI-predicted activityagainst MRSA50+ registered studies
- RisperidoneExisting use: Aggressive behavior, Autism, Bipolar disorder and 4 more66.4% AI-predicted activityagainst MRSA50+ registered studies
- Lazertinib MesylateExisting use: Non-small cell lung carcinoma66.1% AI-predicted activityagainst MRSANo documented evidence found
- Desmopressin AcetateExisting use: Central diabetes insipidus, Diabetes insipidus, Enuresis and 5 more65.8% AI-predicted activityagainst MRSA50+ registered studies
- Terazosin HydrochlorideExisting use: Benign prostatic hyperplasia65.8% AI-predicted activityagainst MRSA41 registered studies
- VemurafenibExisting use: Cancer, Cutaneous melanoma, Melanoma and 2 more65.8% AI-predicted activityagainst MRSA50+ registered studies
- Caspofungin AcetateExisting use: Aspergillosis, Candidemia, Candidiasis and 1 more65.5% AI-predicted activityagainst MRSA50+ registered studies
- VenetoclaxExisting use: Cancer, Chronic lymphocytic leukemia, Neoplasm65.5% AI-predicted activityagainst MRSA50+ registered studies
- Larotrectinib SulfateExisting use: Abdominal Neoplasms, Cancer, Metastasis and 1 more65.4% AI-predicted activityagainst MRSA5 registered studies
- SirolimusExisting use: Adenoma sebaceum, Angiofibroma, Cancer and 5 more65.2% AI-predicted activityagainst MRSA50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Measuring Outcomes In Patients With Pulmonary Arterial Hypertension Not on Active Treatment (MOTION)
NCT02191137 · start 2014-09-23
Registered record
- Registry ID
- NCT02191137
- Conditions
- Hypertension, Pulmonary
- Interventions
- Riociguat (Adempas, BAY63-2521)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2014-09-23
- Completion
- 2016-07-16
- Enrolment
- 75
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension, PulmonaryInterventionRiociguat (Adempas, BAY63-2521)PhasePhase 4Registry statusCompletedEfficacy and Safety of Riociguat in Patients With Symptomatic Pulmonary Hypertension (PH) Associated With Idiopathic Interstitial Pneumonias (IIP)
NCT02138825 · start 2014-06-04
Registered record
- Registry ID
- NCT02138825
- Conditions
- Idiopathic Interstitial Pneumonias / Hypertension,Pulmonary
- Interventions
- Riociguat (Adempas, BAY63-2521); Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2014-06-04
- Completion
- 2016-09-14
- Enrolment
- 147
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIdiopathic Interstitial Pneumonias / Hypertension,PulmonaryInterventionRiociguat (Adempas, BAY63-2521); PlaceboPhasePhase 2Registry statusTerminatedRelative Bioavailability Study
NCT02159313 · start 2014-06
Registered record
- Registry ID
- NCT02159313
- Conditions
- Healthy Volunteers
- Interventions
- Riociguat(Adempas,BAY63-2521)
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2014-06
- Completion
- 2015-01
- Enrolment
- 48
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy VolunteersInterventionRiociguat(Adempas,BAY63-2521)PhasePhase 1Registry statusCompletedEXPERT, EXPosurE Registry RiociguaT in Patients With Pulmonary Hypertension
NCT02092818 · start 2014-05-31
Registered record
- Registry ID
- NCT02092818
- Conditions
- Hypertension, Pulmonary
- Interventions
- Riociguat (Adempas, BAY63-2521)
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2014-05-31
- Completion
- 2018-06-29
- Enrolment
- 1,316
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension, PulmonaryInterventionRiociguat (Adempas, BAY63-2521)PhaseNot recordedRegistry statusCompletedPilot Study to Evaluate Right Ventricular Function With Riociguat in CTEPH
NCT02094001 · start 2014-05
Registered record
- Registry ID
- NCT02094001
- Conditions
- Chronic Thromboembolic Pulmonary Hypertension
- Interventions
- Cardiac PET imaging using F-18-FDG, N-13 ammonia( NH3)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2014-05
- Completion
- 2016-06
- Enrolment
- 6
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Thromboembolic Pulmonary HypertensionInterventionCardiac PET imaging using F-18-FDG, N-13 ammonia( NH3)PhasePhase 2Registry statusCompletedRiociguat Clinical Effects Studied in Patients With Insufficient Treatment Response to Phosphodiesterase-5 Inhibitor
NCT02007629 · start 2014-02-18
Registered record
- Registry ID
- NCT02007629
- Conditions
- Hypertension, Pulmonary
- Interventions
- Riociguat (Adempas, BAY63-2521)
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2014-02-18
- Completion
- 2016-12-29
- Enrolment
- 61
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension, PulmonaryInterventionRiociguat (Adempas, BAY63-2521)PhasePhase 3Registry statusCompletedDigital Flow Enhancement in Raynaud's Phenomenon With an sGC (Soluble Guanylate Cyclase) Stimulator
NCT01926847 · start 2013-10
Registered record
- Registry ID
- NCT01926847
- Conditions
- Raynaud Disease
- Interventions
- Riociguat (Adempas, BAY63-2521); Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2013-10
- Completion
- 2014-06
- Enrolment
- 23
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRaynaud DiseaseInterventionRiociguat (Adempas, BAY63-2521); PlaceboPhasePhase 2Registry statusCompletedCoronary Vasomotor Response After Riociguat Exposure
NCT01165931 · start 2012-05
Registered record
- Registry ID
- NCT01165931
- Conditions
- Coronary Artery Disease
- Interventions
- Riociguat (BAY63-2521)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Withdrawn
- Start
- 2012-05
- Completion
- 2013-01
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronary Artery DiseaseInterventionRiociguat (BAY63-2521)PhasePhase 2Registry statusWithdrawnRelative Bioavailability and Food Effect Study
NCT01489488 · start 2012-01
Registered record
- Registry ID
- NCT01489488
- Conditions
- Pharmacology, Clinical
- Interventions
- Riociguat (BAY63-2521); Riociguat (BAY63-2521); Riociguat (BAY63-2521); Riociguat (BAY63-2521); Riociguat (BAY63-2521)
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2012-01
- Completion
- 2012-05
- Enrolment
- 32
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPharmacology, ClinicalInterventionRiociguat (BAY63-2521); Riociguat (BAY63-2521); Riociguat (BAY63-2521); Riociguat (BAY63-2521) +1 morePhasePhase 1Registry statusCompletedStudy of Incidence of Respiratory Tract AEs in Patients Treated With Tyvaso® Compared to Other FDA Approved PAH Therapies
NCT01266265 · start 2010-12
Registered record
- Registry ID
- NCT01266265
- Conditions
- Pulmonary Arterial Hypertension
- Interventions
- inhaled prostacyclin; inhaled prostacyclin; prostacyclin; subcutaneous and intravenous prostacyclin; oral ERA; oral PDE5 inhibitors
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2010-12
- Completion
- 2014-12
- Enrolment
- 1,333
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonary Arterial HypertensionInterventioninhaled prostacyclin; inhaled prostacyclin; prostacyclin; subcutaneous and intravenous prostacyclin +2 morePhaseNot recordedRegistry statusCompletedEvaluation of the Pharmacodynamic Effect of the Combination of Sildenafil and Riociguat on Blood Pressure and Other Safety Parameters.
NCT01179334 · start 2010-08
Registered record
- Registry ID
- NCT01179334
- Conditions
- Pulmonary Hypertension
- Interventions
- Riociguat (Adempas, BAY63-2521); Placebo; Sildenafil
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2010-08
- Completion
- 2013-05
- Enrolment
- 18
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonary HypertensionInterventionRiociguat (Adempas, BAY63-2521); Placebo; SildenafilPhasePhase 2Registry statusCompletedA Study to Test the Effects of Riociguat in Patients With Pulmonary Hypertension Associated With Left Ventricular Diastolic Dysfunction
NCT01172756 · start 2010-07
Registered record
- Registry ID
- NCT01172756
- Conditions
- Hypertension, Pulmonary; Ventricular Dysfunction, Left
- Interventions
- Riociguat (BAY63-2521); Riociguat (BAY63-2521); Riociguat (BAY63-2521); Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2010-07
- Completion
- 2012-10
- Enrolment
- 39
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension, Pulmonary; Ventricular Dysfunction, LeftInterventionRiociguat (BAY63-2521); Riociguat (BAY63-2521); Riociguat (BAY63-2521); PlaceboPhasePhase 2Registry statusTerminatedStudy on the Safety of BAY 63-2521, How it is Tolerated and the Way the Body Absorbs, Distributes and Gets Rid of the Study Drug Given as a Single Oral Dose of 1 mg Tablet in Participants With Renal Impairment and Healthy Participants Matched for Age-, Gender-, and Weight
NCT04364464 · start 2010-02-19
Registered record
- Registry ID
- NCT04364464
- Conditions
- Clinical Pharmacology
- Interventions
- Riociguat (Adempas, BAY 63-2521)
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2010-02-19
- Completion
- 2011-09-20
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionClinical PharmacologyInterventionRiociguat (Adempas, BAY 63-2521)PhasePhase 1Registry statusCompletedBAY63-2521:Long-term Extension Study in Patients With Pulmonary Arterial Hypertension
NCT00863681 · start 2009-03-12
Registered record
- Registry ID
- NCT00863681
- Conditions
- Hypertension, Pulmonary
- Interventions
- Riociguat (BAY63-2521)
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2009-03-12
- Completion
- 2019-08-19
- Enrolment
- 396
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension, PulmonaryInterventionRiociguat (BAY63-2521)PhasePhase 3Registry statusCompletedA Study to Evaluate Efficacy and Safety of Oral BAY63-2521 in Patients With CTEPH.
NCT00855465 · start 2009-02-23
Registered record
- Registry ID
- NCT00855465
- Conditions
- Pulmonary Hypertension
- Interventions
- Riociguat (Adempas, BAY63-2521); Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2009-02-23
- Completion
- 2012-06-27
- Enrolment
- 262
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonary HypertensionInterventionRiociguat (Adempas, BAY63-2521); PlaceboPhasePhase 3Registry statusCompleted