Paclitaxel
FDA-approved product (injectable, injection), marketed as Abraxane, Paclitaxel, Taxol.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Breast cancer
- Breast carcinoma
- Breast neoplasm
- Cancer
- Carcinoma
- HER2 Positive Breast Carcinoma
- Kaposi's sarcoma
- Malignant Pancreatic Neoplasm
- Neoplasm
- Non-small cell lung carcinoma
- Ovarian cancer
- Ovarian carcinoma
- Ovarian neoplasm
- Pancreatic carcinoma
- Pancreatic neoplasm
- Undifferentiated carcinoma
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Taxanes
- FDA pharmacologic class
- Microtubule 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, 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- MRSA60.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli44.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae33.9% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis42.9% 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 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 Paclitaxel 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.
Ph II Intraperitoneal Paclitaxel + System Therapy in GI Ca w/Peritoneal Carcinomatosis (STOPGAP-B)
NCT07795749 · start 2026-08-04
Registered record
- Registry ID
- NCT07795749
- Conditions
- Esophageal Carcinoma; Gastric Cancer (Diagnosis); Colorectal Adenocarcinoma; Appendiceal Adenocarcinoma; Small Bowel Adenocarcinoma; Hepatobiliary Carcinoma in Situ
- Interventions
- Paclitaxel Q2W; Paclitaxcel Q3W
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2026-08-04
- Completion
- 2029-08-31
- Enrolment
- 55
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEsophageal Carcinoma; Gastric Cancer (Diagnosis); Colorectal Adenocarcinoma; Appendiceal Adenocarcinoma +2 moreInterventionPaclitaxel Q2W; Paclitaxcel Q3WPhasePhase 2Registry statusRecruitingA Study of BL-B01D1 in Combination With Tislelizumab ±5-Fluorouracil Versus Platinum-Based Chemotherapy Plus Tislelizumab as First-line Treatment in Patients With Unresectable, Locally Advanced Recurrent or Metastatic Esophageal Squamous Cell Carcinoma(PANKU-Esophagus02)
NCT07554456 · start 2026-06-09
Registered record
- Registry ID
- NCT07554456
- Conditions
- Esophageal Squamous Cell Carcinoma
- Interventions
- BL-B01D1; Tislelizumab; 5-Fluorouracil; Cisplatin; Paclitaxel
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Recruiting
- Start
- 2026-06-09
- Completion
- 2028-12
- Enrolment
- 90
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEsophageal Squamous Cell CarcinomaInterventionBL-B01D1; Tislelizumab; 5-Fluorouracil; Cisplatin +1 morePhasePhase 2 / Phase 3Registry statusRecruitingA Phase II/III Clinical Study to Evaluate HLX07 in Combination With Serplulimab and Chemotherapy Versus Placebo in Combination With Serplulimab or Pembrolizumab and Chemotherapy as First-Line Treatment in Advanced Squamous Non-Small Cell Lung Cancer
NCT07318883 · start 2026-03
Registered record
- Registry ID
- NCT07318883
- Conditions
- Squamous NSCLC
- Interventions
- HLX07; HLX07 placebo; Serplulimab; Pembrolizumab; Carboplatin; Paclitaxel or Nab-Paclitaxel
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Not yet recruiting
- Start
- 2026-03
- Completion
- 2031-01
- Enrolment
- 720
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSquamous NSCLCInterventionHLX07; HLX07 placebo; Serplulimab; Pembrolizumab +2 morePhasePhase 2 / Phase 3Registry statusNot yet recruitingIparomlimab and Tuvonralimab Plus Chemotherapy for Inducing Conversion to Resectability in Initially Unresectable Stage III NSCLC
NCT07139041 · start 2025-10
Registered record
- Registry ID
- NCT07139041
- Conditions
- NSCLC (Non-small-cell Lung Cancer)
- Interventions
- Iparomlimab and tuvonralimab plus chemotherapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2025-10
- Completion
- 2029-06
- Enrolment
- 69
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNSCLC (Non-small-cell Lung Cancer)InterventionIparomlimab and tuvonralimab plus chemotherapyPhasePhase 2Registry statusNot yet recruitingA Study to Evaluate Two Dosing Regimens of Subcutaneous Nivolumab in Combination With Intravenous Ipilimumab and Chemotherapy in Participants With Previously Untreated Metastatic or Recurrent Non-Small Cell Lung Cancer (NSCLC)
NCT06946797 · start 2025-09-19
Registered record
- Registry ID
- NCT06946797
- Conditions
- Non-Small Cell Lung Cancer
- Interventions
- Nivolumab; Ipilimumab; Carboplatin; Paclitaxel; Pemetrexed; Cisplatin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Active not recruiting
- Start
- 2025-09-19
- Completion
- 2028-10-25
- Enrolment
- 76
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNon-Small Cell Lung CancerInterventionNivolumab; Ipilimumab; Carboplatin; Paclitaxel +2 morePhasePhase 2Registry statusActive not recruitingCombination of Concurrent Chemoradiotherapy With Surufatinib and Tislelizumab in Patients With Locally Advanced Non-Small Cell Lung Cancer
NCT07086456 · start 2025-07-20
Registered record
- Registry ID
- NCT07086456
- Conditions
- Surufatinib; Tislelizumab; Concurrent Chemoradiotherapy; Consolidation Therapy; Non-small Cell Lung Cancer
- Interventions
- Surufatinib; Tislelizumab; Concurrent Chemotherapy; Radiotherapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2025-07-20
- Completion
- 2029-07-19
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSurufatinib; Tislelizumab; Concurrent Chemoradiotherapy; Consolidation Therapy +1 moreInterventionSurufatinib; Tislelizumab; Concurrent Chemotherapy; RadiotherapyPhasePhase 2Registry statusRecruitingClinical Outcomes of Drug-Coated Balloons in the Treatment of Patients With Coronary De Novo Chronic Total Occlusion Lesions
NCT07463664 · start 2025-04-28
Registered record
- Registry ID
- NCT07463664
- Conditions
- Chronic Total Occlusions of Coronary Arteries; Chronic Total Occlusion (CTO); Coronary Artery Disease (CAD)
- Interventions
- DES Implantation; DCB Angioplasty
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2025-04-28
- Completion
- 2026-12-31
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Total Occlusions of Coronary Arteries; Chronic Total Occlusion (CTO); Coronary Artery Disease (CAD)InterventionDES Implantation; DCB AngioplastyPhaseNot applicableRegistry statusRecruitingSUPRAME-ACTengine® IMA203 vs. Investigator's Choice of Treatment in Previously Treated, Unresectable or Metastatic Cutaneous Melanoma
NCT06743126 · start 2025-01-14
Registered record
- Registry ID
- NCT06743126
- Conditions
- Melanoma, Cutaneous Malignant
- Interventions
- IMA203; nivolumab plus relatlimab; lifileucel; nivolumab; pembrolizumab; ipilimumab; Dacarbazine; temozolomide; paclitaxel; paclitaxel plus carboplatin; Albumin-Bound Paclitaxel
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2025-01-14
- Completion
- 2031-10
- Enrolment
- 360
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMelanoma, Cutaneous MalignantInterventionIMA203; nivolumab plus relatlimab; lifileucel; nivolumab +7 morePhasePhase 3Registry statusRecruitingComparing the Efficacy of Sintilimab Plus Nab-POF Regimen, Sintilimab Plus XELOX Chemotherapy, and Lenvatinib, Sintilimab Plus XELOX Chemotherapy in the Treatment of HER2-negative, Metastatic Gastric Cancer
NCT06748508 · start 2024-12-25
Registered record
- Registry ID
- NCT06748508
- Conditions
- Gastric (Stomach) Cancer
- Interventions
- Sintilimab, oxalipaltin, 5FU,Nab-paclitaxel,lenvatinib
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2024-12-25
- Completion
- 2027-12-25
- Enrolment
- 141
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGastric (Stomach) CancerInterventionSintilimab, oxalipaltin, 5FU,Nab-paclitaxel,lenvatinibPhasePhase 2Registry statusNot yet recruitingNeoadjuvant Chemotherapy + PD-1 Inhibitor+Different Radiotherapy Fractionations for HR+/HER2- Breast Cancer
NCT06639672 · start 2024-11-01
Registered record
- Registry ID
- NCT06639672
- Conditions
- HR+HER2- Breast Cancer
- Interventions
- Chemotherapy+PD-1 inhibitor+8Gy x 3f; Chemotherapy+PD-1 inhibitor+16Gy x 1f; Chemotherapy+PD-1 inhibitor+2.67Gy x 15f; Chemotherapy+PD-1 inhibitor+0.5Gy x 12-18f
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2024-11-01
- Completion
- 2031-05-01
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHR+HER2- Breast CancerInterventionChemotherapy+PD-1 inhibitor+8Gy x 3f; Chemotherapy+PD-1 inhibitor+16Gy x 1f; Chemotherapy+PD-1 inhibitor+2.67Gy x 15f; Chemotherapy+PD-1 inhibitor+0.5Gy x 12-18fPhasePhase 2Registry statusNot yet recruiting"The Effect of Memantine on the Prevention and Amelioration of Paclitaxel-induced Toxicity in Breast Cancer Patients"
NCT06679387 · start 2024-10-30
Registered record
- Registry ID
- NCT06679387
- Conditions
- Breast Cancer Early Stage Breast Cancer (Stage 1-3)
- Interventions
- Memantine-HCl; Placebo Oral Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2024-10-30
- Completion
- 2025-10
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBreast Cancer Early Stage Breast Cancer (Stage 1-3)InterventionMemantine-HCl; Placebo Oral TabletPhasePhase 2Registry statusRecruitingAdaptive De-intensified Radiotherapy Using Circulating Tumor DNA in HPV- Associated Oropharyngeal Cancer
NCT06323460 · start 2024-03-21
Registered record
- Registry ID
- NCT06323460
- Conditions
- Clinical Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Oropharyngeal Squamous Cell Carcinoma
- Interventions
- Biospecimen Collection; Carboplatin; Cisplatin; Computed Tomography; External Beam Radiation Therapy; Paclitaxel; Positron Emission Tomography; Questionnaire Administration
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2024-03-21
- Completion
- 2026-12-31
- Enrolment
- 45
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionClinical Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Oropharyngeal Squamous Cell CarcinomaInterventionBiospecimen Collection; Carboplatin; Cisplatin; Computed Tomography +4 morePhasePhase 2Registry statusRecruitingA Study of ASKG915 in Patients With Selected Advanced Solid Tumors.
NCT05867420 · start 2023-08-02
Registered record
- Registry ID
- NCT05867420
- Conditions
- Advanced Solid Tumors
- Interventions
- ASKG915; Paclitaxel + Bevacizumab; Fruquintinib; Docetaxel
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Recruiting
- Start
- 2023-08-02
- Completion
- 2028-06-30
- Enrolment
- 594
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAdvanced Solid TumorsInterventionASKG915; Paclitaxel + Bevacizumab; Fruquintinib; DocetaxelPhasePhase 1 / Phase 2Registry statusRecruitingRole of Silymarin in Chemotherapy Toxicity and Cognition Improvement in Breast Cancer Patients
NCT05595109 · start 2022-10-28
Registered record
- Registry ID
- NCT05595109
- Conditions
- Breast Cancer; Peripheral Neuropathy; Cardiac Toxicities; Hepatic Toxicity; Cognitive Impairment
- Interventions
- Silymarin; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Unknown
- Start
- 2022-10-28
- Completion
- 2024-10-28
- Enrolment
- 56
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBreast Cancer; Peripheral Neuropathy; Cardiac Toxicities; Hepatic Toxicity +1 moreInterventionSilymarin; PlaceboPhasePhase 2 / Phase 3Registry statusUnknownThe Efficacy and Safety of Sintilimab Plus Anlotinib Combined With Chemotherapy as Neoadjuvant Therapy in TNBC
NCT04877821 · start 2021-09-15
Registered record
- Registry ID
- NCT04877821
- Conditions
- Triple Negative Breast Cancer
- Interventions
- Sintilimab; Anlotinib; Nab paclitaxel; Carboplatin; Epirubicin; Cyclophosphamide
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2021-09-15
- Completion
- 2026-03-10
- Enrolment
- 29
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTriple Negative Breast CancerInterventionSintilimab; Anlotinib; Nab paclitaxel; Carboplatin +2 morePhasePhase 2Registry statusCompleted