Levofloxacin Anhydrous
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Also known as Levofloxacin (anhydrous)Levofloxacine (anhydrous)Levofloxacino (anhydrous)NSC-758709Ofloxacin s-(-)-formLevofloxacinLevoflaxacinLevoflaxin
Summary
Levofloxacin Anhydrous (CHEMBL33) is an approved small-molecule DNA synthesis inhibitor; indicated across 4 conditions including overactive bladder and tuberculosis.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- Indications: 4 conditions
- Clinical trials: 204
- Chemistry: C18H20FN3O4
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL33 |
| Name | Levofloxacin Anhydrous |
| Type | Small molecule |
| Max phase | 4 |
| ChEBI | CHEBI:63598 |
| Molecular formula | C18H20FN3O4 |
| InChIKey | GSDSWSVVBLHKDQ-JTQLQIEISA-N |
SMILES: C[C@H]1COc2c(N3CCN(C)CC3)c(F)cc3c(=O)c(C(=O)O)cn1c23
ChEBI definition: An optically active form of ofloxacin having (S)-configuration; an inhibitor of bacterial topoisomerase IV and DNA gyrase.
Pharmacological roles (ChEBI): DNA synthesis inhibitor, antibacterial drug, topoisomerase IV inhibitor, EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor.
Also known as: Levofloxacin (anhydrous), Levofloxacin anhydrous, Levofloxacine (anhydrous), Levofloxacino (anhydrous), NSC-758709, Ofloxacin s-(-)-form, LEVOFLOXACIN ANHYDROUS, Levofloxacin, levofloxacin, Levoflaxacin, Levoflaxin
Parent form; salt/anhydrous children: CHEMBL2237108, CHEMBL5315124
Patent coverage: 14,240 distinct patent families (43,403 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Broader ChEMBL bioactivity targets: 1 (assay-derived). Sample: Tubulin.
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
4 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| overactive bladder | 1 | MONDO:0006624 | EFO:1000781 |
| tuberculosis | 1 | MONDO:0018076 | MONDO:0018076 |
| osteomyelitis | 0 | MONDO:0005246 | EFO:0003102 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 204.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 63 |
| PHASE3 | 62 |
| Not specified | 30 |
| PHASE2 | 21 |
| PHASE2/PHASE3 | 11 |
| PHASE1 | 10 |
| PHASE1/PHASE2 | 6 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05061732 | PHASE4 | RECRUITING | Helicobacter Pylori Eradication and Follow-up |
| NCT05398679 | PHASE4 | RECRUITING | Oral Antimicrobial Treatment vs. Outpatient Parenteral for Infective Endocarditis |
| NCT06172010 | PHASE4 | RECRUITING | Rifampicin Combination Therapy Versus Monotherapy for Staphylococcal Prosthetic Joint Infection |
| NCT06200779 | PHASE4 | NOT_YET_RECRUITING | Tailored Vs. Empirical Helicobacter Pylori Infection Treatment |
| NCT06494072 | PHASE4 | RECRUITING | Short Versus Standard of Care Antibiotic Duration for Children Hospitalized for CAP |
| NCT06741917 | PHASE4 | ENROLLING_BY_INVITATION | Retrograde Intrarenal Surgery Low Risk Trial |
| NCT07021729 | PHASE4 | NOT_YET_RECRUITING | Comparison of Two Treatment Regimens of Helicobacter Pylori Infection |
| NCT07040839 | PHASE4 | NOT_YET_RECRUITING | Comparison of Omeprazole vs Vonoprazon in Treatment of H Pylori Infection |
| NCT07320534 | PHASE4 | NOT_YET_RECRUITING | Levofloxacin Prophylaxis to Prevent First Febrile Neutropenia in Pediatric ALL During Induction Phase |
| NCT00035347 | PHASE4 | COMPLETED | Intravenous Azithromycin Plus Intravenous Ceftriaxone Followed by Oral Azithromycin With Intravenous Levofloxacin Followed by Oral Levofloxacin for the Treatment of Moderate to Severely Ill Hospitalized Patients With Community Acquired Pneumonia |
| NCT00239161 | PHASE4 | TERMINATED | Safety and Efficacy Study of the Treatment of Kidney Infections With Short Course Levofloxacin |
| NCT00245791 | PHASE4 | TERMINATED | Urinary Tract Infection Study With the Antibiotic Levofloxacin Given at a Higher Dose Over a Shorter Period of Time |
| NCT00392275 | PHASE4 | COMPLETED | Penetrance of Third Generation Fluoroquinolones in Eyes With Functioning Filtering Blebs |
| NCT00429975 | PHASE4 | TERMINATED | Ceftriaxone Vs Levofloxacin on Cytokine Expression in Pneumococcal Pneumonia |
| NCT00495339 | PHASE4 | COMPLETED | MDR TB, Levofloxacin, Multi-Drug-Resistant Pulmonary Tuberculosis |
| NCT00645073 | PHASE4 | COMPLETED | Study of the Safety and Efficacy of Cefdinir and Levofloxacin for the Treatment of Subjects With Acute Bacterial Sinusitis |
| NCT00665327 | PHASE4 | COMPLETED | Avelox for Treatment of Elderly Patients With Community Acquired Pneumonia |
| NCT00752947 | PHASE4 | UNKNOWN | Efficacy and Safety Trial to Assess Moxifloxacin in Treating Community-Acquired Pneumonia (CAP) With Aspiration Factors |
| NCT00840580 | PHASE4 | COMPLETED | Effect on Wound Healing of Vigamox Versus Cravit |
| NCT01034176 | PHASE4 | COMPLETED | BK Treatment Study |
| NCT01353339 | PHASE4 | COMPLETED | Quinolone Prophylaxis for the Prevention of BK Virus Infection in Kidney Transplantation: A Pilot Study |
| NCT01467297 | PHASE4 | COMPLETED | Ceftidoren Versus Levofloxacin in the Treatment of Patients With Acute Exacerbations of Chronic Bronchitis (AECB) |
| NCT01524302 | PHASE4 | COMPLETED | Pharmacodynamic of Ceftaroline and Levofloxacin Against Pathogens Associated With Community Acquired Bacterial Pneumonia |
| NCT01742429 | PHASE4 | COMPLETED | Levofloxacin and Bismuth-containing Therapy Versus Quadruple Therapy as Second-line Treatment of Resistant Helicobacter Pylori Infection |
| NCT02018081 | PHASE4 | COMPLETED | Pharmacokinetics of Levofloxacin in Intensive Care Unit |
| NCT02028754 | PHASE4 | COMPLETED | A Study of Sodium Carboxymethylcellulose for Post Cataract Surgery Dry Eye Symptoms |
| NCT02094703 | PHASE4 | UNKNOWN | The Efficacy of Solifenacin Succinate as Adjuvant Therapy for Urinary Tract Infection in Females |
| NCT02466919 | PHASE4 | COMPLETED | Study of Levofloxacin-based Concomitant Therapy for H. Pylori Eradication in Diabetic Patients |
| NCT02600806 | PHASE4 | UNKNOWN | Clinical Pathway Based on Procalcitonin Levels for the Management of Community-acquired Pneumonia in Outpatients |
| NCT02618057 | PHASE4 | UNKNOWN | Effects of Oral Steroid in Mycoplasma Pneumoniae Pneumonia |
| NCT02693574 | PHASE4 | UNKNOWN | Comparison Efficacy of 14-day Triple Therapy: Clarithromycin vs. Levofloxacin on Eradication of H. Pylori |
| NCT02757365 | PHASE4 | UNKNOWN | Efficiency Study of Aspirin to Prevent the Occurrence of Prostate Cancer |
| NCT02901288 | PHASE4 | UNKNOWN | Shortened Regimens for Drug-susceptible Pulmonary Tuberculosis |
| NCT02935010 | PHASE4 | COMPLETED | Tailored Versus Empiric Therapy for Helicobacter Pylori Treatment |
| NCT02988089 | PHASE4 | UNKNOWN | Antimicrobial Susceptibility Testing Guided Antibiotic Selection Strategies in Salvage Helicobacter Pylori Treatment |
| NCT03087656 | PHASE4 | UNKNOWN | Antibiotics to Decrease Post ERCP Cholangitis |
| NCT03139253 | PHASE4 | UNKNOWN | Antimicrobial Susceptibility Testing Guided Triple Therapy in Salvage Helicobacter Pylori Treatment |
| NCT03160807 | PHASE4 | UNKNOWN | Levofloxacin as an Empirical Therapy in Patients With Complicated Urinary Tract Infections |
| NCT03413020 | PHASE4 | COMPLETED | Tailored Therapy for Helicobacter Pylori Rescue Treatment |
| NCT03555526 | PHASE4 | UNKNOWN | Genotypic Resistance Guided Therapy for Refractory H. Pylori Infection |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.