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 M. tuberculosis and MRSA. 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.
- Mefloquine HydrochlorideExisting use: Malaria, Plasmodium falciparum malaria, Plasmodium vivax malaria81.8% AI-predicted activityagainst M. tuberculosisLab records exist8 registered studies
- KetoconazoleExisting use: Adrenal gland disease, Blastomycosis, Cushing syndrome and 3 more81.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- LevoketoconazoleExisting use: Adrenal gland disease, Adrenal gland hyperfunction, Cushing syndrome81.2% AI-predicted activityagainst M. tuberculosis6 registered studies
- Fluphenazine DecanoateExisting use: Mental or behavioural disorder, Psychosis80.7% AI-predicted activityagainst M. tuberculosis4 registered studies
- Fluphenazine EnanthateExisting use: Mental or behavioural disorder, Psychosis80.7% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- NifurtimoxExisting use: American trypanosomiasis, Chagas disease, Leishmaniasis and 1 more78.4% AI-predicted activityagainst M. tuberculosis19 registered studies
- Fluphenazine HydrochlorideExisting use: Mental or behavioural disorder, Psychosis77.8% AI-predicted activityagainst M. tuberculosis5 registered studies
- NitazoxanideExisting use: Amebiasis, Diarrhea77.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- TopiramateExisting use: Epilepsy, Lennox-Gastaut syndrome, Migraine disorder and 1 more77.4% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- TrabectedinExisting use: Cancer, Dedifferentiated liposarcoma, Leiomyosarcoma and 7 more76.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Chlorpromazine HydrochlorideExisting use: Conduct disorder, Mental or behavioural disorder, Nausea and vomiting and 3 more75.0% AI-predicted activityagainst M. tuberculosis33 registered studies
- ProchlorperazineExisting use: Anxiety disorder, Nausea and vomiting, Psychosis and 1 more74.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Discontinuation Versus Continuation of Riociguat Monotherapy in Chronic Thromboembolic Pulmonary Hypertension Successfully Treated With Balloon Pulmonary Angioplasty
NCT07644377 · start 2026-11-01
Registered record
- Registry ID
- NCT07644377
- Conditions
- CTEPH
- Interventions
- Discontinuation of riociguat
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Not yet recruiting
- Start
- 2026-11-01
- Completion
- 2031-01-31
- Enrolment
- 150
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCTEPHInterventionDiscontinuation of riociguatPhasePhase 3Registry statusNot yet recruitingRiociguat in Triple Therapy for Pulmonary Arterial Hypertension in Real-World Practice
NCT07374302 · start 2026-03-01
Registered record
- Registry ID
- NCT07374302
- Conditions
- Pulmonary Arterial Hypertension
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Not yet recruiting
- Start
- 2026-03-01
- Completion
- 2026-12-31
- Enrolment
- 15
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonary Arterial HypertensionInterventionNot recordedPhaseNot recordedRegistry statusNot yet recruitingA Study of Sotatercept for Patients With Eisenmenger Syndrome or Unrepaired Shunt-Associated Pulmonary Arterial Hypertension Resistant to Vasodilator Therapy
NCT07356778 · start 2025-10-07
Registered record
- Registry ID
- NCT07356778
- Conditions
- Eisenmenger Syndrome; Pulmonary Arterial Hypertension of Congenital Heart Disease
- Interventions
- Sotatercept; vasodilator-based PAH therapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2025-10-07
- Completion
- 2028-04-30
- Enrolment
- 36
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEisenmenger Syndrome; Pulmonary Arterial Hypertension of Congenital Heart DiseaseInterventionSotatercept; vasodilator-based PAH therapyPhasePhase 4Registry statusRecruitingRiociguat-Discontinue Effects on Right HEART in CTEPH (RED-HEART)
NCT06922240 · start 2025-03-21
Registered record
- Registry ID
- NCT06922240
- Conditions
- Chronic Thromboembolic Pulmonary Hypertension
- Interventions
- Riociguat; Routine Treatment
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2025-03-21
- Completion
- 2027-10-31
- Enrolment
- 68
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Thromboembolic Pulmonary HypertensionInterventionRiociguat; Routine TreatmentPhasePhase 3Registry statusRecruitingEffects of Combination Medical Therapy Followed by BPA on Right Ventricular-PA Coupling and Hemodynamics in CTEPH
NCT05140525 · start 2025-01-27
Registered record
- Registry ID
- NCT05140525
- Conditions
- CTEPH
- Interventions
- Macitentan Tablets; Riociguat; balloon pulmonary angioplasty
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Terminated
- Start
- 2025-01-27
- Completion
- 2026-05-01
- Enrolment
- 7
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCTEPHInterventionMacitentan Tablets; Riociguat; balloon pulmonary angioplastyPhasePhase 3Registry statusTerminatedEfficacy and Safety of Triple-targeted Drug Therapy in Treatment-naive Patients With Non-low-risk PAH: A Real-world, Multicenter Study
NCT06753981 · start 2024-12-10
Registered record
- Registry ID
- NCT06753981
- Conditions
- Arterial Pulmonary Hypertension (PAH)
- Interventions
- Endothelin receptor antagonist (ERA) combined with PDE5i/sGC agonist dual therapy prostacyclin drugs
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2024-12-10
- Completion
- 2027-02-14
- Enrolment
- 48
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionArterial Pulmonary Hypertension (PAH)InterventionEndothelin receptor antagonist (ERA) combined with PDE5i/sGC agonist dual therapy prostacyclin drugsPhaseNot recordedRegistry statusRecruitingSwitching of Sildenafil to Riociguat in CTEPH Patients
NCT06715280 · start 2024-07-25
Registered record
- Registry ID
- NCT06715280
- Conditions
- Chronic Thromboembolic Pulmonary Hypertension
- Interventions
- Riociguat (Adempas)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2024-07-25
- Completion
- 2027-01-22
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Thromboembolic Pulmonary HypertensionInterventionRiociguat (Adempas)PhasePhase 4Registry statusRecruitingEffect of Riocigaut on Migraine Attack Induction in People With Migraine
NCT05750446 · start 2023-06-01
Registered record
- Registry ID
- NCT05750446
- Conditions
- Migraine Without Aura
- Interventions
- Riociguat (BAY 63-2521); Placebo
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2023-06-01
- Completion
- 2024-02-01
- Enrolment
- 22
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMigraine Without AuraInterventionRiociguat (BAY 63-2521); PlaceboPhaseNot applicableRegistry statusCompletedBioequivalence Study of Riociguat 2.5 mg Film Coated Tablets and Adempas (Riociguat) 2.5 mg Film Coated Tablets
NCT06180096 · start 2023-03-07
Registered record
- Registry ID
- NCT06180096
- Conditions
- Pulmonary Arterial Hypertension
- Interventions
- Riociguat film coated tablets; Adempas Filmtabletten
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2023-03-07
- Completion
- 2023-04-06
- Enrolment
- 36
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonary Arterial HypertensionInterventionRiociguat film coated tablets; Adempas FilmtablettenPhasePhase 1Registry statusCompletedEffect of Riocigaut on Cerebral Vasodilation and Headache Induction in Healthy Volunteers
NCT05582811 · start 2022-10-26
Registered record
- Registry ID
- NCT05582811
- Conditions
- Headache
- Interventions
- Dose Riociguat 2,5 or 5mg; Riociguat; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2022-10-26
- Completion
- 2023-06-01
- Enrolment
- 15
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHeadacheInterventionDose Riociguat 2,5 or 5mg; Riociguat; PlaceboPhaseNot applicableRegistry statusCompletedNetworked Drug REpurposing for Mechanism-based neuroPrOtection in Acute Ischaemic STROKE
NCT05762146 · start 2022-09-05
Registered record
- Registry ID
- NCT05762146
- Conditions
- Ischemic Stroke, Acute
- Interventions
- Riociguat; Propylthiouracil; Perphenazine
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2022-09-05
- Completion
- 2024-04-30
- Enrolment
- 28
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIschemic Stroke, AcuteInterventionRiociguat; Propylthiouracil; PerphenazinePhasePhase 2Registry statusUnknownA Study to Learn About How Well Riociguat Works, How Safe it is and How it is Used Under Real World Conditions in Patients in the United States Who Are Receiving Riociguat for High Blood Pressure in the Arteries That Carry Blood From the Heart to the Lungs (Pulmonary Arterial Hypertension, PAH)
NCT04813926 · start 2021-07-16
Registered record
- Registry ID
- NCT04813926
- Conditions
- Pulmonary Arterial Hypertension
- Interventions
- Riociguat (Adempas, BAY63-2521)
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2021-07-16
- Completion
- 2025-02-03
- Enrolment
- 500
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonary Arterial HypertensionInterventionRiociguat (Adempas, BAY63-2521)PhaseNot recordedRegistry statusCompletedInitial Dual Oral Combination Therapy Versus Standard-of-care Initial Oral Monotherapy Prior to Balloon Pulmonary Angioplasty in Patients With Inoperable Chronic Thromboembolic Pulmonary Hypertension
NCT04780932 · start 2021-06-14
Registered record
- Registry ID
- NCT04780932
- Conditions
- Thromboembolic Pulmonary Hypertension; Chronic Disease; Inoperable Disease
- Interventions
- Macitentan 10mg; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Completed
- Start
- 2021-06-14
- Completion
- 2025-07-03
- Enrolment
- 96
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionThromboembolic Pulmonary Hypertension; Chronic Disease; Inoperable DiseaseInterventionMacitentan 10mg; PlaceboPhasePhase 2 / Phase 3Registry statusCompletedPossible Effects of Propylthiouracil, Riociguat and Perphenazine on Circulation of Healthy Volunteers
NCT04776499 · start 2021-03-18
Registered record
- Registry ID
- NCT04776499
- Conditions
- Drug Drug Interaction; Safety Issues
- Interventions
- Propylthiouracil, Riociguat, Perphenazine
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2021-03-18
- Completion
- 2022-02-28
- Enrolment
- 8
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDrug Drug Interaction; Safety IssuesInterventionPropylthiouracil, Riociguat, PerphenazinePhasePhase 1Registry statusCompletedTHERAPY-HYBRID-BPA Trial
NCT04600492 · start 2020-10-16
Registered record
- Registry ID
- NCT04600492
- Conditions
- Hypertension, Pulmonary
- Interventions
- Riociguat Oral Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2020-10-16
- Completion
- 2025-01-28
- Enrolment
- 72
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension, PulmonaryInterventionRiociguat Oral TabletPhasePhase 2Registry statusUnknown