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Sulfamethoxazole

FDA-approved product (tablet, oral), marketed as Gantanol, Gantanol-Ds, Sulfamethoxazole and 1 more.

Registered studies
50+
Lab records
17
Pathogens at ≥40%
1 of 4

Chemical structure

Chemical structure of Sulfamethoxazole
A drawing shows what the molecule is, not what it does.

Existing / approved use

Documented · FDA, WHO, ChEMBL

Approved for

  • Bacterial disease
  • Infection
  • Pneumocystosis
  • Urinary tract infection

Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗

WHO therapeutic group
Intermediate-acting sulfonamides
Anti-infective classification
Classified as an existing antimicrobial.WHO ATC J01EC01

Repurposing investigation

Sulfamethoxazole 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
  • MRSA30.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
  • E. coli22.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
  • K. pneumoniae5.4% 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. tuberculosis65.6% 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 evidence

Clinical

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

  • K. pneumoniae: measured active in 0 of 17 lab records
Show the 17 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 measured

Dihydrofolate reductase ↗ (E. coli)

-7.3 kcal/mol

0better fit →-12

KPC-2 carbapenemase ↗ (K. pneumoniae)

-7.7 kcal/mol

0better fit →-12

Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)

-7.3 kcal/mol

0better fit →-12

Dihydrofolate reductase ↗ (MRSA)

-7.6 kcal/mol

0better fit →-12

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 measured

Other repurposing candidates: approved medicines besides Sulfamethoxazole 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.

Registered studies

A registration describes a study; it does not establish a positive result.

  • Early Methicillin-resistant Staphylococcus Aureus (MRSA) Therapy in Cystic Fibrosis (CF)

    NCT01349192 · start 2011-04

    Registered record
    Registry ID
    NCT01349192
    Conditions
    Cystic Fibrosis; Methicillin-resistant Staphylococcus Aureus
    Interventions
    Rifampin; Trimethoprim/Sulfamethoxazole; Minocycline; Mupirocin; chlorhexidine gluconate oral rinse; 2% Chlorhexidine solution wipes; Environmental Decontamination
    Study type
    INTERVENTIONAL
    Phase
    Phase 2
    Registry status
    Terminated
    Start
    2011-04
    Completion
    2015-05
    Enrolment
    47

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionCystic Fibrosis; Methicillin-resistant Staphylococcus Aureus
    InterventionRifampin; Trimethoprim/Sulfamethoxazole; Minocycline; Mupirocin +3 more
    PhasePhase 2
    Registry statusTerminated
  • Chemopreventive Therapy for Malaria in Ugandan Children

    NCT00948896 · start 2010-06

    Registered record
    Registry ID
    NCT00948896
    Conditions
    Malaria
    Interventions
    trimethoprim-sulfamethoxazole (TS; TMP/SMX); sulfadoxine-pyrimethamine (SP); dihydroartemisinin-piperaquine (DP)
    Study type
    INTERVENTIONAL
    Phase
    Phase 3
    Registry status
    Completed
    Start
    2010-06
    Completion
    2014-04
    Enrolment
    600

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionMalaria
    Interventiontrimethoprim-sulfamethoxazole (TS; TMP/SMX); sulfadoxine-pyrimethamine (SP); dihydroartemisinin-piperaquine (DP)
    PhasePhase 3
    Registry statusCompleted
  • Randomized Controlled Trial of Antibiotics in the Management of Children With Community-Acquired Abscess

    NCT01498744 · start 2010-02

    Registered record
    Registry ID
    NCT01498744
    Conditions
    Abscess Soft Tissue; Methicillin-resistant Staphylococcus Aureus (MRSA) Infection; Skin Abscess
    Interventions
    Oral Clindamycin
    Study type
    INTERVENTIONAL
    Phase
    Not applicable
    Registry status
    Terminated
    Start
    2010-02
    Completion
    2013-02
    Enrolment
    53

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionAbscess Soft Tissue; Methicillin-resistant Staphylococcus Aureus (MRSA) Infection; Skin Abscess
    InterventionOral Clindamycin
    PhaseNot applicable
    Registry statusTerminated
  • Single Dose Monurol for Treatment of Acute Cystitis

    NCT00976963 · start 2009-09-17

    Registered record
    Registry ID
    NCT00976963
    Conditions
    Urinary Tract Infection
    Interventions
    TMP/SMX; Fosfomycin
    Study type
    INTERVENTIONAL
    Phase
    Not applicable
    Registry status
    Completed
    Start
    2009-09-17
    Completion
    2016-12-27
    Enrolment
    300

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionUrinary Tract Infection
    InterventionTMP/SMX; Fosfomycin
    PhaseNot applicable
    Registry statusCompleted
  • Cotrimoxazole Prophylaxis Cessation Study Among Stabilized HIV-Infected Adult Patients on HAART in Entebbe, Uganda

    NCT00674921 · start 2008-06

    Registered record
    Registry ID
    NCT00674921
    Conditions
    HIV Infections
    Interventions
    cotrimoxazole; Placebo
    Study type
    INTERVENTIONAL
    Phase
    Phase 4
    Registry status
    Unknown
    Start
    2008-06
    Completion
    2011-06
    Enrolment
    1,650

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionHIV Infections
    Interventioncotrimoxazole; Placebo
    PhasePhase 4
    Registry statusUnknown
  • Prospective 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.

    ConditionAbscesses
    Interventionbactrim; placebo
    PhasePhase 3
    Registry statusCompleted
  • Orally Administered Trimethoprim-sulfamethoxazole and Metronidazole as Prophylaxis of Infection Following Elective Colorectal Surgery

    NCT00613769 · start 2007-09

    Registered record
    Registry ID
    NCT00613769
    Conditions
    Infection Prophylaxis in Colo Rectal Surgery
    Interventions
    trimethoprim-sulfamethoxazole + metronidazole; cefuroxime and metronidazole
    Study type
    INTERVENTIONAL
    Phase
    Phase 4
    Registry status
    Completed
    Start
    2007-09
    Completion
    2012-05
    Enrolment
    1,073

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionInfection Prophylaxis in Colo Rectal Surgery
    Interventiontrimethoprim-sulfamethoxazole + metronidazole; cefuroxime and metronidazole
    PhasePhase 4
    Registry statusCompleted
  • Antibiotic Treatment Duration for Non-Surgically-Treated Diabetic Foot Osteomyelitis

    NCT02123628 · start 2007-06

    Registered record
    Registry ID
    NCT02123628
    Conditions
    Diabetes Mellitus
    Interventions
    duration of the antibiotic therapy
    Study type
    INTERVENTIONAL
    Phase
    Phase 4
    Registry status
    Completed
    Start
    2007-06
    Completion
    2012-09
    Enrolment
    40

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionDiabetes Mellitus
    Interventionduration of the antibiotic therapy
    PhasePhase 4
    Registry statusCompleted
  • Computer Stop Order Alert to Prevent Concurrent Prescribing of Trimethoprim/Sulfamethoxazole and Warfarin

    NCT00870298 · start 2006-08

    Registered record
    Registry ID
    NCT00870298
    Conditions
    Prescribers' Drug Orders
    Interventions
    Trimethoprim/Sulfamethoxazole and Warfarin
    Study type
    INTERVENTIONAL
    Phase
    Not applicable
    Registry status
    Terminated
    Start
    2006-08
    Completion
    2007-01
    Enrolment
    1,971

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionPrescribers' Drug Orders
    InterventionTrimethoprim/Sulfamethoxazole and Warfarin
    PhaseNot applicable
    Registry statusTerminated
  • Daily Isoniazid to Prevent Tuberculosis in Infants Born to Mothers With HIV

    NCT00080119 · start 2004-02

    Registered record
    Registry ID
    NCT00080119
    Conditions
    HIV Infection; Tuberculosis; Pneumocystis Jiroveci Pneumonia
    Interventions
    Isoniazid (INH); Trimethoprim/Sulfamethoxazole (TMP/SMX); Isoniazid Placebo (PL)
    Study type
    INTERVENTIONAL
    Phase
    Phase 2 / Phase 3
    Registry status
    Terminated
    Start
    2004-02
    Completion
    2009-05
    Enrolment
    1,354

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionHIV Infection; Tuberculosis; Pneumocystis Jiroveci Pneumonia
    InterventionIsoniazid (INH); Trimethoprim/Sulfamethoxazole (TMP/SMX); Isoniazid Placebo (PL)
    PhasePhase 2 / Phase 3
    Registry statusTerminated
  • VNP20009 in Treating Patients With Advanced or Metastatic Solid Tumors That Have Not Responded to Previous Therapy

    NCT00004216 · start 1999-08

    Registered record
    Registry ID
    NCT00004216
    Conditions
    Unspecified Adult Solid Tumor, Protocol Specific
    Interventions
    salmonella VNP20009; cefixime; ceftriaxone sodium; ciprofloxacin; trimethoprim-sulfamethoxazole
    Study type
    INTERVENTIONAL
    Phase
    Phase 1
    Registry status
    Completed
    Start
    1999-08
    Completion
    2008-01
    Enrolment
    Not recorded

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionUnspecified Adult Solid Tumor, Protocol Specific
    Interventionsalmonella VNP20009; cefixime; ceftriaxone sodium; ciprofloxacin +1 more
    PhasePhase 1
    Registry statusCompleted
  • High Dose Sequential Therapy and Autologous Stem Cell Rescue for Multiple Myeloma

    NCT00586014 · start 1997-05

    Registered record
    Registry ID
    NCT00586014
    Conditions
    Multiple Myeloma
    Interventions
    High-Dose Sequential Chemotherapy followed by ASCT
    Study type
    INTERVENTIONAL
    Phase
    Phase 2
    Registry status
    Completed
    Start
    1997-05
    Completion
    2008-02
    Enrolment
    91

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionMultiple Myeloma
    InterventionHigh-Dose Sequential Chemotherapy followed by ASCT
    PhasePhase 2
    Registry statusCompleted
  • Antibiotic Therapy in Preventing Early Infection in Patients With Multiple Myeloma Who Are Receiving Chemotherapy

    NCT00002850 · start 1997-03

    Registered record
    Registry ID
    NCT00002850
    Conditions
    Infection; Multiple Myeloma
    Interventions
    ciprofloxacin; ofloxacin; 160 mg trimethoprim and 800 mg sulfamethoxazole
    Study type
    INTERVENTIONAL
    Phase
    Phase 3
    Registry status
    Completed
    Start
    1997-03
    Completion
    2012-01
    Enrolment
    212

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionInfection; Multiple Myeloma
    Interventionciprofloxacin; ofloxacin; 160 mg trimethoprim and 800 mg sulfamethoxazole
    PhasePhase 3
    Registry statusCompleted
  • Chemotherapy With or Without Surgery, Radiation Therapy, or Stem Cell Transplantation in Treating Young Patients With Kidney Tumors

    NCT00002610 · start 1996-01

    Registered record
    Registry ID
    NCT00002610
    Conditions
    Kidney Cancer
    Interventions
    dactinomycin; filgrastim; carboplatin; cyclophosphamide; doxorubicin hydrochloride; etoposide; vincristine sulfate; conventional surgery; radiation therapy
    Study type
    INTERVENTIONAL
    Phase
    Phase 3
    Registry status
    Completed
    Start
    1996-01
    Completion
    2006-02
    Enrolment
    203

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionKidney Cancer
    Interventiondactinomycin; filgrastim; carboplatin; cyclophosphamide +5 more
    PhasePhase 3
    Registry statusCompleted
  • A Randomized, Double-Blind Study of 566C80 Versus Septra (Sulfamethoxazole/Trimethoprim) for the Treatment of Pneumocystis Carinii Pneumonia in AIDS Patients

    NCT00000655

    Registered record
    Registry ID
    NCT00000655
    Conditions
    Pneumonia, Pneumocystis Carinii; HIV Infections
    Interventions
    Atovaquone; Sulfamethoxazole-Trimethoprim
    Study type
    INTERVENTIONAL
    Phase
    Phase 2
    Registry status
    Completed
    Start
    Not recorded
    Completion
    Not recorded
    Enrolment
    300

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionPneumonia, Pneumocystis Carinii; HIV Infections
    InterventionAtovaquone; Sulfamethoxazole-Trimethoprim
    PhasePhase 2
    Registry statusCompleted