Vismodegib
FDA-approved product (capsule, oral), marketed as Erivedge.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Basal cell carcinoma
- Cancer
- Neoplasm
- Skin basal cell carcinoma
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Hedgehog pathway inhibitors
- FDA pharmacologic class
- Hedgehog Pathway 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 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- MRSA46.7% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli27.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae11.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis65.8% 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 Vismodegib 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.
- FurazolidoneExisting use: Other antiinfectives and antiseptics91.4% AI-predicted activityagainst M. tuberculosisLab records exist49 registered studies
- TriflupromazineExisting use: Psychosis90.6% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- ValdecoxibExisting use: Dysmenorrhea, Osteoarthritis, Rheumatic disease and 1 more88.6% AI-predicted activityagainst M. tuberculosisLab records exist31 registered studies
- CelecoxibExisting use: Ankylosing spondylitis, Cancer, Colorectal neoplasm and 15 more87.6% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Dorzolamide HydrochlorideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma86.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- MethazolamideExisting use: Glaucoma, Open-angle glaucoma85.6% AI-predicted activityagainst M. tuberculosisLab records exist11 registered studies
- AcetazolamideExisting use: Altitude sickness, Angle-closure glaucoma, Congestive heart failure and 5 more85.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Trifluoperazine HydrochlorideExisting use: Anxiety disorder, Mental or behavioural disorder, Psychosis and 1 more84.6% AI-predicted activityagainst M. tuberculosis1 registered study
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives84.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- NitrofurazoneExisting use: Eye infection, Leishmaniasis, Trypanosomiasis84.0% AI-predicted activityagainst M. tuberculosis8 registered studies
- BrinzolamideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma83.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- ZonisamideExisting use: Epilepsy, Focal-onset seizure, Partial epilepsy and 1 more82.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Vismodegib in Treating Patients With Recurrent or Refractory Medulloblastoma
NCT00939484 · start 2009-06
Registered record
- Registry ID
- NCT00939484
- Conditions
- Adult Medulloblastoma
- Interventions
- Pharmacological Study; Vismodegib
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2009-06
- Completion
- 2015-08
- Enrolment
- 31
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAdult MedulloblastomaInterventionPharmacological Study; VismodegibPhasePhase 2Registry statusCompletedGDC-0449 and Erlotinib Hydrochloride With or Without Gemcitabine Hydrochloride in Treating Patients With Metastatic Pancreatic Cancer or Solid Tumors That Cannot Be Removed by Surgery
NCT00878163 · start 2009-03-31
Registered record
- Registry ID
- NCT00878163
- Conditions
- Adult Solid Neoplasm; Pancreatic Acinar Cell Carcinoma; Pancreatic Ductal Adenocarcinoma; Recurrent Pancreatic Carcinoma; Stage IV Pancreatic Cancer AJCC v6 and v7
- Interventions
- Diagnostic Laboratory Biomarker Analysis; Erlotinib Hydrochloride; Gemcitabine Hydrochloride; Vismodegib
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Active not recruiting
- Start
- 2009-03-31
- Completion
- 2027-03-06
- Enrolment
- 55
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAdult Solid Neoplasm; Pancreatic Acinar Cell Carcinoma; Pancreatic Ductal Adenocarcinoma; Recurrent Pancreatic Carcinoma +1 moreInterventionDiagnostic Laboratory Biomarker Analysis; Erlotinib Hydrochloride; Gemcitabine Hydrochloride; VismodegibPhasePhase 1Registry statusActive not recruitingGDC-0449 in Treating Young Patients With Medulloblastoma That is Recurrent or Did Not Respond to Previous Treatment
NCT00822458 · start 2009-01
Registered record
- Registry ID
- NCT00822458
- Conditions
- Recurrent Childhood Medulloblastoma
- Interventions
- vismodegib; laboratory biomarker analysis; pharmacological study
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2009-01
- Completion
- Not recorded
- Enrolment
- 34
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRecurrent Childhood MedulloblastomaInterventionvismodegib; laboratory biomarker analysis; pharmacological studyPhasePhase 1Registry statusCompletedA Study of Vismodegib (GDC-0449, Hedgehog Pathway Inhibitor) With Concurrent Chemotherapy and Bevacizumab As First-Line Therapy for Metastatic Colorectal Cancer
NCT00636610 · start 2008-05
Registered record
- Registry ID
- NCT00636610
- Conditions
- Metastatic Colorectal Cancer
- Interventions
- Vismodegib 150 mg; Placebo to vismodegib; Bevacizumab; Modified FOLFOX; FOLFIRI
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2008-05
- Completion
- 2010-12
- Enrolment
- 199
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMetastatic Colorectal CancerInterventionVismodegib 150 mg; Placebo to vismodegib; Bevacizumab; Modified FOLFOX +1 morePhasePhase 2Registry statusCompletedGDC-0449 in Treating Patients With Locally Advanced or Metastatic Solid Tumors
NCT00607724 · start 2007-04
Registered record
- Registry ID
- NCT00607724
- Conditions
- Unspecified Adult Solid Tumor, Protocol Specific
- Interventions
- GDC-0449
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2007-04
- Completion
- 2009-11
- Enrolment
- 68
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionUnspecified Adult Solid Tumor, Protocol SpecificInterventionGDC-0449PhasePhase 1Registry statusCompleted