Methicillin Sodium
FDA-approved product (injectable, injection), marketed as Staphcillin.
- Registered studies
- 50+
- Lab records
- 29
- Pathogens at ≥40%
- 0 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Bacterial disease
Indications ChEMBL records as approved, from FDA and DailyMed labels.
- WHO therapeutic group
- Beta-lactamase resistant penicillins
- Anti-infective classification
- Classified as an existing antimicrobial.WHO ATC J01CF03
Repurposing investigation
Methicillin Sodium is already an antimicrobial, so it is not counted among the repurposing candidates. Its AI-predicted activity is shown below for reference.
AI-predicted activity
AI prediction · nothing measured- MRSA10.3% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
- E. coli4.3% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
- K. pneumoniae10.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
- M. tuberculosis35.6% AI-predicted activityBelow 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
- MRSA: measured active in 8 of 26 lab records
- E. coli: measured active in 0 of 2 lab records
- K. pneumoniae: measured active in 0 of 1 lab record
Show the 29 laboratory records, with sources
Loading records…
“Active” means the measured value reached this project’s laboratory cutoff (10 µM or stronger). A laboratory result does not show an effect in patients.
Docking
Computational · nothing measuredDihydrofolate reductase ↗ (E. coli)
Not yet docked: queued in the docking rundetails
KPC-2 carbapenemase ↗ (K. pneumoniae)
Not yet docked: queued in the docking rundetails
Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)
Not yet docked: queued in the docking rundetails
Dihydrofolate 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 Methicillin Sodium 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.
- Etrasimod ArginineExisting use: Ulcerative colitis64.1% AI-predicted activityagainst MRSANo documented evidence found
- MethotrexateExisting use: Acute lymphoblastic leukemia, Adenoma, Arthritis and 21 more64.1% AI-predicted activityagainst MRSA50+ registered studies
- KetoconazoleExisting use: Adrenal gland disease, Blastomycosis, Cushing syndrome and 3 more63.6% AI-predicted activityagainst MRSA50+ registered studies
- LevoketoconazoleExisting use: Adrenal gland disease, Adrenal gland hyperfunction, Cushing syndrome63.6% AI-predicted activityagainst MRSA6 registered studies
- Nafarelin AcetateExisting use: Endometriosis63.6% AI-predicted activityagainst MRSA12 registered studies
- Pafolacianine SodiumExisting use: Other diagnostic agents63.6% AI-predicted activityagainst MRSA1 registered study
- Vinorelbine TartrateExisting use: Cancer, Neoplasm63.6% AI-predicted activityagainst MRSA50+ registered studies
- Ibrexafungerp CitrateExisting use: Vulvovaginal candidiasis63.5% AI-predicted activityagainst MRSANo documented evidence found
- Gonadorelin AcetateExisting use: Gonadotropin-releasing hormones, Tests for fertility disturbances63.4% AI-predicted activityagainst MRSA50+ registered studies
- Icatibant AcetateExisting use: Angioedema, Hereditary angioedema63.4% AI-predicted activityagainst MRSA33 registered studies
- LonafarnibExisting use: Hutchinson-Gilford progeria syndrome, Laminopathies, Progeria63.3% AI-predicted activityagainst MRSA39 registered studies
- LypressinExisting use: Vasopressin and analogues63.2% AI-predicted activityagainst MRSA50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Efficacy Study of Altabax to Clear Methicillin-resistant Staphylococcus Aureus (MRSA) Nasal Colonization
NCT00856089 · start 2009-05
Registered record
- Registry ID
- NCT00856089
- Conditions
- Methicillin-resistant Staphylococcus Aureus
- Interventions
- Retapamulin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Withdrawn
- Start
- 2009-05
- Completion
- 2009-10
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMethicillin-resistant Staphylococcus AureusInterventionRetapamulinPhasePhase 4Registry statusWithdrawnRetapamulin Versus Linezolid in the Treatment of SITL and Impetigo Due to MRSA
NCT00852540 · start 2009-04
Registered record
- Registry ID
- NCT00852540
- Conditions
- Skin Infections, Bacterial
- Interventions
- Retpamulin Ointment, 1%; Linezolid
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2009-04
- Completion
- 2010-09
- Enrolment
- 410
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSkin Infections, BacterialInterventionRetpamulin Ointment, 1%; LinezolidPhasePhase 3Registry statusCompletedImmunologic Predisposition of HIV Patients to Develop Methicillin-Resistant Staphylococcus Aureus (MRSA) Colonization and Infection
NCT00859677 · start 2009-03
Registered record
- Registry ID
- NCT00859677
- Conditions
- HIV Infections; Staphylococcal Infections
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2009-03
- Completion
- 2016-08-26
- Enrolment
- 52
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV Infections; Staphylococcal InfectionsInterventionNot recordedPhaseNot recordedRegistry statusCompletedClinical Trial on the Reduction of Methicillin Resistant Staphylococcus Aureus (MRSA)
NCT00790608 · start 2009-01
Registered record
- Registry ID
- NCT00790608
- Conditions
- Skin Ulcers; Methicillin-resistant Staphylococcus Aureus Infection
- Interventions
- Nitric Oxide
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2009-01
- Completion
- 2011-08
- Enrolment
- 8
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSkin Ulcers; Methicillin-resistant Staphylococcus Aureus InfectionInterventionNitric OxidePhasePhase 2Registry statusTerminatedEmergency Bedside Ultrasound for Pediatric Soft Tissue Infections
NCT00595881 · start 2008-07
Registered record
- Registry ID
- NCT00595881
- Conditions
- Abscess
- Interventions
- Bedside emergency ultrasound
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2008-07
- Completion
- 2010-05
- Enrolment
- 420
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAbscessInterventionBedside emergency ultrasoundPhaseNot recordedRegistry statusCompletedStaphylococcus Aureus Decolonization Study
NCT00731783 · start 2008-07
Registered record
- Registry ID
- NCT00731783
- Conditions
- Staphylococcal Skin Infections; Abscesses; Furunculosis; Staphylococcus Aureus; MRSA Infection
- Interventions
- 2% Mupirocin Ointment; 4% Chlorhexidine liquid soap; Hygiene protocol
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2008-07
- Completion
- 2010-12
- Enrolment
- 183
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionStaphylococcal Skin Infections; Abscesses; Furunculosis; Staphylococcus Aureus +1 moreIntervention2% Mupirocin Ointment; 4% Chlorhexidine liquid soap; Hygiene protocolPhaseNot applicableRegistry statusCompletedTwo Strategies for Methicillin-resistant Staphylococcus Aureus (MRSA) Infection Prevention in Surgical Patients
NCT00685867 · start 2008-05
Registered record
- Registry ID
- NCT00685867
- Conditions
- MRSA Infection
- Interventions
- Rapid molecular MRSA test; Hand hygiene promotion
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2008-05
- Completion
- 2010-12
- Enrolment
- 126,750
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMRSA InfectionInterventionRapid molecular MRSA test; Hand hygiene promotionPhaseNot applicableRegistry statusCompletedA Prospective Cohort Pilot Study of the Clinical and Molecular Epidemiology of Staphylococcus Aureus in Pregnant Women at the Time of Group B Streptococcal Screening in a Large Urban Medical Center in Chicago, IL USA
NCT00532324 · start 2008-02
Registered record
- Registry ID
- NCT00532324
- Conditions
- Staphylococcus Aureus
- Interventions
- CA-MRSA Decolonization
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2008-02
- Completion
- 2013-10
- Enrolment
- 107
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionStaphylococcus AureusInterventionCA-MRSA DecolonizationPhaseNot applicableRegistry statusCompletedIncidence and Relationship of Positive Preoperative Methicillin Resistant Staphylococcus Aureus (MRSA) Screens and Post-operative Infections
NCT01028105 · start 2008-02
Registered record
- Registry ID
- NCT01028105
- Conditions
- Methicillin-resistant Staphylococcus Aureus Infection
- Interventions
- Preoperative MRSA screening
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Terminated
- Start
- 2008-02
- Completion
- 2013-10
- Enrolment
- 975
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMethicillin-resistant Staphylococcus Aureus InfectionInterventionPreoperative MRSA screeningPhaseNot applicableRegistry statusTerminatedProspective Randomized Trial of Bactrim on 7 Day Outcome in Patients With Uncomplicated Abscesses
NCT00973765 · start 2007-11
Registered record
- Registry ID
- NCT00973765
- Conditions
- Abscesses
- Interventions
- bactrim; placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2007-11
- Completion
- 2009-08
- Enrolment
- 212
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAbscessesInterventionbactrim; placeboPhasePhase 3Registry statusCompletedProspective Study of Methicillin-Resistant Staphylococcus Aureus (MRSA) Among HIV-Infected Persons
NCT00631566 · start 2007-05
Registered record
- Registry ID
- NCT00631566
- Conditions
- HIV Infections; Staphylococcal Infections
- Interventions
- Mupirocin (Bactroban) 2%; hexachlorophene (pHisoHex) 3%; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2007-05
- Completion
- 2017-10
- Enrolment
- 550
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV Infections; Staphylococcal InfectionsInterventionMupirocin (Bactroban) 2%; hexachlorophene (pHisoHex) 3%; PlaceboPhaseNot applicableRegistry statusCompletedComparative Study of Ceftaroline vs. Vancomycin Plus Aztreonam in Adult Subjects With Complicated Skin Infections
NCT00423657 · start 2007-03
Registered record
- Registry ID
- NCT00423657
- Conditions
- Bacterial Infections
- Interventions
- ceftaroline; vancomycin plus aztreonam; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2007-03
- Completion
- 2007-12
- Enrolment
- 680
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBacterial InfectionsInterventionceftaroline; vancomycin plus aztreonam; PlaceboPhasePhase 3Registry statusCompletedStudy Evaluating the Safety and Efficacy of a Once-daily Dose of Tigecycline vs Ertapenem in Diabetic Foot Infections (DFI) With a Substudy in Patients With Diabetic Foot Infections Complicated by Osteomyelitis.
NCT00366249 · start 2007-01
Registered record
- Registry ID
- NCT00366249
- Conditions
- Bacterial Infections; Diabetic Foot; Osteomyelitis
- Interventions
- Tigecycline; Ertapenem
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2007-01
- Completion
- 2009-03
- Enrolment
- 1,061
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBacterial Infections; Diabetic Foot; OsteomyelitisInterventionTigecycline; ErtapenemPhasePhase 3Registry statusCompletedComparison of Cephalexin Versus Clindamycin for Suspected CA-MRSA Skin Infections
NCT00352612 · start 2006-09
Registered record
- Registry ID
- NCT00352612
- Conditions
- Staphylococcal Infection; Abscess; Staphylococcal Skin Infection; Folliculitis
- Interventions
- clindamycin; cephalexin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2006-09
- Completion
- 2009-08
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionStaphylococcal Infection; Abscess; Staphylococcal Skin Infection; FolliculitisInterventionclindamycin; cephalexinPhasePhase 4Registry statusCompletedStudy Comparing the Safety and Efficacy of Tigecycline With Ampicillin-Sulbactam or Amoxicillin-Clavulanate to Treat Skin Infections
NCT00368537 · start 2006-09
Registered record
- Registry ID
- NCT00368537
- Conditions
- Skin Diseases, Bacterial
- Interventions
- Tigecycline; ampicillin-sulbactam
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2006-09
- Completion
- 2008-09
- Enrolment
- 550
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSkin Diseases, BacterialInterventionTigecycline; ampicillin-sulbactamPhasePhase 4Registry statusCompleted