Levoleucovorin
FDA-approved product (powder, intravenous), marketed as Khapzory, Fusilev, Levoleucovorin Calcium.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Anemia
- Colorectal adenocarcinoma
- Colorectal cancer
- Colorectal carcinoma
- Colorectal neoplasm
- Osteosarcoma
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Detoxifying agents for antineoplastic treatment
- 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, E. coli and K. pneumoniae. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA52.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli67.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae43.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- M. tuberculosis54.8% 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 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 Levoleucovorin 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.
- DichlorphenamideExisting use: Glaucoma73.9% AI-predicted activityagainst M. tuberculosisLab records exist2 registered studies
- Tamsulosin HydrochlorideExisting use: Benign prostatic hyperplasia, Prostate carcinoma73.2% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Thiethylperazine MalateExisting use: Allergic disease71.8% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- SaquinavirExisting use: HIV infection, HIV-1 infection, Viral disease71.5% AI-predicted activityagainst M. tuberculosis50+ registered studies
- AvacopanExisting use: Anti-neutrophil antibody associated vasculitis, Anti-neutrophil cytoplasmic antibody-associated vasculitis, Granulomatosis with Polyangiitis and 1 more71.3% AI-predicted activityagainst M. tuberculosis26 registered studies
- Lasmiditan SuccinateExisting use: Migraine disorder71.0% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma71.0% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Vinblastine SulfateExisting use: Classic Hodgkin lymphoma, Fungal infectious disease, Hodgkins lymphoma and 3 more70.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Haloperidol DecanoateExisting use: Conduct disorder, Mental or behavioural disorder, Psychosis and 4 more70.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
- HydrochlorothiazideExisting use: Angina pectoris, Cardiovascular disease, Chronic kidney disease and 9 more70.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
- TolvaptanExisting use: Autosomal dominant polycystic kidney disease, Cardiovascular disease, Congestive heart failure and 4 more70.0% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Larotrectinib SulfateExisting use: Abdominal Neoplasms, Cancer, Metastasis and 1 more69.2% AI-predicted activityagainst M. tuberculosis5 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Personalize (Signature Driven) Neoadjuvant Chemotherapy Trial for Patients With Resectable Borderline Pancreatic Ductal Adenocarcinoma.
NCT07616362 · start 2026-06
Registered record
- Registry ID
- NCT07616362
- Conditions
- Borderline Resectable Pancreatic Ductal Adenocarcinoma
- Interventions
- Nab paclitaxel / gemcitabine; mFOLFIRINOX
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-06
- Completion
- 2031-04
- Enrolment
- 110
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBorderline Resectable Pancreatic Ductal AdenocarcinomaInterventionNab paclitaxel / gemcitabine; mFOLFIRINOXPhasePhase 2Registry statusNot yet recruitingSurufatinib Plus mFOLFIRINOX and PD-1 Inhibitor as the Neoadjuvant Therapy for High-risk or Borderline Resectable Pancreatic Cancer
NCT07469956 · start 2026-03-31
Registered record
- Registry ID
- NCT07469956
- Conditions
- Pancreatic Cancer Resectable
- Interventions
- Surufatinib; Toripalimab; mFOLFIRINOX
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-03-31
- Completion
- 2029-01-31
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPancreatic Cancer ResectableInterventionSurufatinib; Toripalimab; mFOLFIRINOXPhasePhase 2Registry statusNot yet recruitingNeoadjuvant Therapy for the Treatment of Gastroesophageal Junction and Gastric Cancers
NCT05296005 · start 2025-12-31
Registered record
- Registry ID
- NCT05296005
- Conditions
- Clinical Stage I Gastric Cancer AJCC v8; Clinical Stage II Gastric Cancer AJCC v8; Clinical Stage IIA Gastric Cancer AJCC v8; Clinical Stage IIB Gastric Cancer AJCC v8; Clinical Stage IIB Gastroesophageal Junction Adenocarcinoma AJCC v8; Clinical Stage III Gastric Cancer AJCC v8; Clinical Stage III Gastroesophageal Junction Adenocarcinoma AJCC v8; Clinical Stage IVA Gastroesophageal Junction Adenocarcinoma AJCC v8; Gastric Adenocarcinoma; Pathologic Stage IB Gastric Cancer AJCC v8; Pathologic Stage IC Gastroesophageal Junction Adenocarcinoma AJCC v8; Pathologic Stage II Gastric Cancer AJCC v8; Pathologic Stage II Gastroesophageal Junction Adenocarcinoma AJCC v8; Pathologic Stage IIA Gastric Cancer AJCC v8; Pathologic Stage IIA Gastroesophageal Junction Adenocarcinoma AJCC v8; Pathologic Stage IIB Gastric Cancer AJCC v8; Pathologic Stage IIB Gastroesophageal Junction Adenocarcinoma AJCC v8; Pathologic Stage III Gastric Cancer AJCC v8; Pathologic Stage III Gastroesophageal Junction Adeno
- Interventions
- Capecitabine; Docetaxel; Fluorouracil; Leucovorin; Oxaliplatin; Radiation Therapy; Surgical Procedure
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Withdrawn
- Start
- 2025-12-31
- Completion
- 2025-12-31
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionClinical Stage I Gastric Cancer AJCC v8; Clinical Stage II Gastric Cancer AJCC v8; Clinical Stage IIA Gastric Cancer AJCC v8; Clinical Stage IIB Gastric Cancer AJCC v8 +15 moreInterventionCapecitabine; Docetaxel; Fluorouracil; Leucovorin +3 morePhasePhase 1Registry statusWithdrawnRefractory Advanced diGestive Neuroendocrine Carcinomas Treated With tARlatamab
NCT07061080 · start 2025-12-18
Registered record
- Registry ID
- NCT07061080
- Conditions
- Advanced Neuroendocrine Carcinomas of The Digestive System; Advanced Neuroendocrine Carcinomas Unknown Primary Origin
- Interventions
- Tarlatamab; standard of care second-line chemotherapy (FOLFIRI)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2025-12-18
- Completion
- 2026-09-03
- Enrolment
- 1
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAdvanced Neuroendocrine Carcinomas of The Digestive System; Advanced Neuroendocrine Carcinomas Unknown Primary OriginInterventionTarlatamab; standard of care second-line chemotherapy (FOLFIRI)PhasePhase 2Registry statusTerminatedSecond-line Irinotecan Liposome Combination Regimen for Irinotecan-treated Pancreatic Cancer
NCT06700603 · start 2024-11-20
Registered record
- Registry ID
- NCT06700603
- Conditions
- Pancreatic Cancer
- Interventions
- Irinotecan liposome (Nal-IRI) in combination with 5-FU/sodium levofolinate
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2024-11-20
- Completion
- 2026-12-31
- Enrolment
- 48
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPancreatic CancerInterventionIrinotecan liposome (Nal-IRI) in combination with 5-FU/sodium levofolinatePhasePhase 2Registry statusNot yet recruitingA Study of Amivantamab and mFOLFOX6 or FOLFIRI Versus Cetuximab and mFOLFOX6 or FOLFIRI as First-line Treatment in Participants With KRAS/NRAS and BRAF Wild-type Unresectable or Metastatic Left-sided Colorectal Cancer
NCT06662786 · start 2024-10-18
Registered record
- Registry ID
- NCT06662786
- Conditions
- Colorectal Neoplasms
- Interventions
- Amivantamab; Cetuximab; 5-fluorouracil; Leucovorin calcium/Levoleucovorin; Oxaliplatin; Irinotecan Hydrochloride
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2024-10-18
- Completion
- 2032-01-20
- Enrolment
- 1,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionColorectal NeoplasmsInterventionAmivantamab; Cetuximab; 5-fluorouracil; Leucovorin calcium/Levoleucovorin +2 morePhasePhase 3Registry statusRecruitingA Study to Learn About the Study Medicine PF-07934040 When Given Alone or With Other Anti-cancer Therapies in People With Advanced Solid Tumors That Have a Genetic Mutation.
NCT06447662 · start 2024-06-27
Registered record
- Registry ID
- NCT06447662
- Conditions
- Carcinoma, Pancreatic Ductal; Colorectal Neoplasms; Carcinoma, Non-Small-Cell Lung
- Interventions
- PF-07934040; Gemcitabine; Nab-paclitaxel; Cetuximab; Fluorouracil; Oxaliplatin; Leucovorin; Bevacizumab; Pembrolizumab; pemetrexed; Cisplatin; Paclitaxel; Carboplatin; Sasanlimab
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Active not recruiting
- Start
- 2024-06-27
- Completion
- 2026-10-09
- Enrolment
- 64
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCarcinoma, Pancreatic Ductal; Colorectal Neoplasms; Carcinoma, Non-Small-Cell LungInterventionPF-07934040; Gemcitabine; Nab-paclitaxel; Cetuximab +10 morePhasePhase 1Registry statusActive not recruitingTrial Evaluating Modified FOLFIRINOX and Modified FOLFOX in the Treatment of Locally Advanced or Metastatic Small Bowel Adenocarcinoma
NCT06278545 · start 2024-02-16
Registered record
- Registry ID
- NCT06278545
- Conditions
- Locally Advanced or Metastatic Small Bowel Adenocarcinoma
- Interventions
- modified FOLFORINOX; Modified FOLFOX
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2024-02-16
- Completion
- 2029-02
- Enrolment
- 130
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLocally Advanced or Metastatic Small Bowel AdenocarcinomaInterventionmodified FOLFORINOX; Modified FOLFOXPhasePhase 2Registry statusRecruitingPhase II Study of the Combination of Irinotecan and POF (POFI) and Tislelizumab in Advanced Gastric Cancer
NCT06197438 · start 2024-01-01
Registered record
- Registry ID
- NCT06197438
- Conditions
- Gastric Cancer
- Interventions
- Tislelizumab; Oxaliplatin; Levo-Leucovorin; 5-fluorouracil; Irinotecan Hydrochloride; Paclitaxel
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2024-01-01
- Completion
- 2025-04-01
- Enrolment
- 36
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGastric CancerInterventionTislelizumab; Oxaliplatin; Levo-Leucovorin; 5-fluorouracil +2 morePhasePhase 2Registry statusUnknownThe ADAPTA Study: ADjuvant chemotherAPy After Curative Intent resecTion of Ampullary Cancer.
NCT06068023 · start 2023-07-01
Registered record
- Registry ID
- NCT06068023
- Conditions
- Ampullary Adenocarcinoma
- Interventions
- Folfirinox; Capox
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2023-07-01
- Completion
- 2029-07-01
- Enrolment
- 400
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAmpullary AdenocarcinomaInterventionFolfirinox; CapoxPhaseNot recordedRegistry statusRecruitingLEAC-102 for Advanced Colorectal Cancer
NCT02826837 · start 2022-09-01
Registered record
- Registry ID
- NCT02826837
- Conditions
- Advanced Colorectal Cancer
- Interventions
- LEAC-102 500mg capsule and FOLFOX + Bevacizumab/Cetuximab
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Unknown
- Start
- 2022-09-01
- Completion
- 2024-02-01
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAdvanced Colorectal CancerInterventionLEAC-102 500mg capsule and FOLFOX + Bevacizumab/CetuximabPhasePhase 1 / Phase 2Registry statusUnknownFOLFOX/FOLFIRI Containing Levofolinic Acid (Zuoyu ®) in the Treatment of Unresectable or Metastatic Colorectal Cancer
NCT05797883 · start 2022-08-01
Registered record
- Registry ID
- NCT05797883
- Conditions
- Unresectable or Metastatic Colorectal Cancer
- Interventions
- FOLFOX/FOLFIRI
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2022-08-01
- Completion
- 2024-12-01
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionUnresectable or Metastatic Colorectal CancerInterventionFOLFOX/FOLFIRIPhasePhase 2Registry statusUnknownA Study to Compare Onivyde Manufactured at Two Different Production Sites in Adult Participants With Advanced Cancer in the Pancreas
NCT05383352 · start 2022-05-30
Registered record
- Registry ID
- NCT05383352
- Conditions
- Metastatic Pancreatic Adenocarcinoma
- Interventions
- Irinotecan liposome injection; Irinotecan liposome injection; Irinotecan liposome injection; Irinotecan liposome injection; Folinic Acid; 5-Fluorouracil
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2022-05-30
- Completion
- 2025-04-15
- Enrolment
- 177
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMetastatic Pancreatic AdenocarcinomaInterventionIrinotecan liposome injection; Irinotecan liposome injection; Irinotecan liposome injection; Irinotecan liposome injection +2 morePhasePhase 1Registry statusCompletedFOLFOXIRI for Neoadjuvant Treatment of High-risk Locally Advanced Colorectal Cancer
NCT05018182 · start 2021-08-02
Registered record
- Registry ID
- NCT05018182
- Conditions
- High-risk Locally Advanced Colorectal Cancer; Neoadjuvant Chemotherapy; FOLFOXIRI Regimen
- Interventions
- Oxaliplatin; Irinotecan; Folinic Acid; 5FU; Capecitabine
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2021-08-02
- Completion
- 2022-08-02
- Enrolment
- 69
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHigh-risk Locally Advanced Colorectal Cancer; Neoadjuvant Chemotherapy; FOLFOXIRI RegimenInterventionOxaliplatin; Irinotecan; Folinic Acid; 5FU +1 morePhasePhase 2Registry statusUnknownNeoOPTIMIZE: Early Switching of mFOLFIRINOX or Gemcitabine/Nab-Paclitaxel Before Surgery for the Treatment of Resectable, Borderline Resectable, or Locally-Advanced Unresectable Pancreatic Cancer
NCT04539808 · start 2021-05-27
Registered record
- Registry ID
- NCT04539808
- Conditions
- Pancreatic Adenocarcinoma; Stage 0 Pancreatic Cancer American Joint Committee on Cancer v8; Stage I Pancreatic Cancer American Joint Committee on Cancer v8; Stage III Pancreatic Cancer American Joint Committee on Cancer v8; Stage IV Pancreatic Cancer American Joint Committee on Cancer v8
- Interventions
- Capecitabine; Fluorouracil; Irinotecan Hydrochloride; Leucovorin Calcium; Losartan Potassium; Oxaliplatin; Radiation Therapy; Resection; Diagnostic Imaging; Biospecimen Collection; Gemcitabine; Nab paclitaxel
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Active not recruiting
- Start
- 2021-05-27
- Completion
- 2027-01-05
- Enrolment
- 42
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPancreatic Adenocarcinoma; Stage 0 Pancreatic Cancer American Joint Committee on Cancer v8; Stage I Pancreatic Cancer American Joint Committee on Cancer v8; Stage III Pancreatic Cancer American Joint Committee on Cancer v8 +1 moreInterventionCapecitabine; Fluorouracil; Irinotecan Hydrochloride; Leucovorin Calcium +8 morePhasePhase 2Registry statusActive not recruiting