Risdiplam
FDA-approved product (for solution, oral), marketed as Evrysdi.
- Registered studies
- 33
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Atrophy
- Proximal spinal muscular atrophy
- Spinal muscular atrophy
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Other drugs for disorders of the musculo-skeletal system
- 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, MRSA and E. coli. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA54.8% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli42.7% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae35.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis55.1% 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
33registered studies name this medicine, for any condition. 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 Risdiplam 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.
A Study to Investigate the Safety and Efficacy of RO7204239 in Combination With Risdiplam (RO7034067) in Participants With Spinal Muscular Atrophy
NCT05115110 · start 2022-06-02
Registered record
- Registry ID
- NCT05115110
- Conditions
- Spinal Muscular Atrophy (SMA)
- Interventions
- RO7204239; Placebo; Risdiplam
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Active not recruiting
- Start
- 2022-06-02
- Completion
- 2026-10-28
- Enrolment
- 97
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSpinal Muscular Atrophy (SMA)InterventionRO7204239; Placebo; RisdiplamPhasePhase 2 / Phase 3Registry statusActive not recruitingEfficacy and Safety of Apitegromab in Patients With Later-Onset Spinal Muscular Atrophy Treated With Nusinersen or Risdiplam
NCT05156320 · start 2022-04-14
Registered record
- Registry ID
- NCT05156320
- Conditions
- Spinal Muscular Atrophy; Spinal Muscular Atrophy Type 3; Spinal Muscular Atrophy Type 2; SMA; Neuromuscular Diseases; Muscular Atrophy; Atrophy; Muscular Atrophy, Spinal; Neuromuscular Manifestations; Anti-myostatin
- Interventions
- Apitegromab; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2022-04-14
- Completion
- 2024-12-18
- Enrolment
- 188
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSpinal Muscular Atrophy; Spinal Muscular Atrophy Type 3; Spinal Muscular Atrophy Type 2; SMA +6 moreInterventionApitegromab; PlaceboPhasePhase 3Registry statusCompletedLong-term Follow-up Study of Risdiplam in Participants With Spinal Muscular Atrophy (SMA)
NCT05232929 · start 2022-03-29
Registered record
- Registry ID
- NCT05232929
- Conditions
- Spinal Muscular Atrophy
- Interventions
- Risdiplam
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Active not recruiting
- Start
- 2022-03-29
- Completion
- 2026-10-02
- Enrolment
- 403
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSpinal Muscular AtrophyInterventionRisdiplamPhasePhase 4Registry statusActive not recruitingA Study to Learn About the Effect of Higher Doses of Nusinersen (BIIB058) Given as Injections to Participants With Spinal Muscular Atrophy (SMA) Who Were Previously Treated With Risdiplam (ASCEND)
NCT05067790 · start 2022-01-21
Registered record
- Registry ID
- NCT05067790
- Conditions
- Spinal Muscular Atrophy
- Interventions
- Nusinersen
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Active not recruiting
- Start
- 2022-01-21
- Completion
- 2027-09-24
- Enrolment
- 45
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSpinal Muscular AtrophyInterventionNusinersenPhasePhase 3Registry statusActive not recruitingInvestigating NMJ Defects in SMA Following Central and Peripheral SMN Restoration
NCT05219487 · start 2021-10-13
Registered record
- Registry ID
- NCT05219487
- Conditions
- Spinal Muscular Atrophy
- Interventions
- Risdiplam
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2021-10-13
- Completion
- 2025-12-31
- Enrolment
- 18
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSpinal Muscular AtrophyInterventionRisdiplamPhaseNot recordedRegistry statusCompletedBioavailability and Bioequivalence of Two Risdiplam Tablets in Healthy Participants
NCT04718181 · start 2021-02-01
Registered record
- Registry ID
- NCT04718181
- Conditions
- Muscular Atrophy, Spinal
- Interventions
- risdiplam; omeprazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2021-02-01
- Completion
- 2023-01-28
- Enrolment
- 131
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMuscular Atrophy, SpinalInterventionrisdiplam; omeprazolePhasePhase 1Registry statusCompletedA Study of Risdiplam in Infants With Genetically Diagnosed and Presymptomatic Spinal Muscular Atrophy
NCT03779334 · start 2019-08-07
Registered record
- Registry ID
- NCT03779334
- Conditions
- Muscular Atrophy, Spinal
- Interventions
- Risdiplam
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Active not recruiting
- Start
- 2019-08-07
- Completion
- 2027-02-28
- Enrolment
- 26
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMuscular Atrophy, SpinalInterventionRisdiplamPhasePhase 2Registry statusActive not recruitingA Drug-drug Interaction Study With Risdiplam Multiple Dose and Midazolam in Healthy Participants
NCT03988907 · start 2019-06-18
Registered record
- Registry ID
- NCT03988907
- Conditions
- Spinal Muscular Atrophy
- Interventions
- Risdiplam; Midazolam
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2019-06-18
- Completion
- 2019-09-29
- Enrolment
- 35
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSpinal Muscular AtrophyInterventionRisdiplam; MidazolamPhasePhase 1Registry statusCompletedA Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics and Safety and Tolerability of a Single Oral Dose of Risdiplam Compared to Matched Healthy Participants With Normal Hepatic Function
NCT03920865 · start 2019-05-16
Registered record
- Registry ID
- NCT03920865
- Conditions
- Muscular Atrophy, Spinal
- Interventions
- Risdiplam
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2019-05-16
- Completion
- 2020-01-02
- Enrolment
- 26
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMuscular Atrophy, SpinalInterventionRisdiplamPhasePhase 1Registry statusCompletedHolter of Movement in Patients with SMA Undergoing Treatment.
NCT04888702 · start 2018-08-08
Registered record
- Registry ID
- NCT04888702
- Conditions
- Spinal Muscular Atrophy
- Interventions
- Actimyo
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2018-08-08
- Completion
- 2025-05-30
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSpinal Muscular AtrophyInterventionActimyoPhaseNot applicableRegistry statusUnknownA Study to Investigate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Risdiplam (RO7034067) in Healthy Japanese Participants
NCT03040635 · start 2017-03-22
Registered record
- Registry ID
- NCT03040635
- Conditions
- Healthy Volunteers
- Interventions
- Risdiplam; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2017-03-22
- Completion
- 2017-10-02
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy VolunteersInterventionRisdiplam; PlaceboPhasePhase 1Registry statusCompletedA Study of Risdiplam (RO7034067) in Adult and Pediatric Participants With Spinal Muscular Atrophy
NCT03032172 · start 2017-03-03
Registered record
- Registry ID
- NCT03032172
- Conditions
- Spinal Muscular Atrophy
- Interventions
- Risdiplam
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2017-03-03
- Completion
- 2025-02-07
- Enrolment
- 174
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSpinal Muscular AtrophyInterventionRisdiplamPhasePhase 2Registry statusCompletedA Study Investigating the Excretion Balance, Pharmacokinetics and Metabolism of a Single Oral Dose of [14C]-Labeled Risdiplam (RO7034067) in Healthy Male Participants
NCT03036501 · start 2017-01-03
Registered record
- Registry ID
- NCT03036501
- Conditions
- Healthy
- Interventions
- [^14C]-Risdiplam
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2017-01-03
- Completion
- 2017-02-28
- Enrolment
- 6
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyIntervention[^14C]-RisdiplamPhasePhase 1Registry statusCompletedInvestigate Safety, Tolerability, PK, PD and Efficacy of Risdiplam (RO7034067) in Infants With Type1 Spinal Muscular Atrophy
NCT02913482 · start 2016-12-23
Registered record
- Registry ID
- NCT02913482
- Conditions
- Muscular Atrophy, Spinal
- Interventions
- Risdiplam
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2016-12-23
- Completion
- 2023-12-22
- Enrolment
- 62
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMuscular Atrophy, SpinalInterventionRisdiplamPhasePhase 2Registry statusCompletedA Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy of Risdiplam (RO7034067) in Type 2 and 3 Spinal Muscular Atrophy (SMA) Participants
NCT02908685 · start 2016-10-19
Registered record
- Registry ID
- NCT02908685
- Conditions
- Muscular Atrophy, Spinal
- Interventions
- Placebo; Risdiplam
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2016-10-19
- Completion
- 2023-10-02
- Enrolment
- 231
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMuscular Atrophy, SpinalInterventionPlacebo; RisdiplamPhasePhase 2Registry statusCompleted