Leucovorin Calcium
FDA-approved product (for solution, oral), marketed as Leucovorin Calcium, Leucovorin Calcium Preservative Free, Vykoura and 1 more.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- 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 MRSA, E. coli, K. pneumoniae and M. tuberculosis. 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 Leucovorin Calcium 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.
- Ozanimod HydrochlorideExisting use: Multiple sclerosis, Relapsing-remitting multiple sclerosis, Ulcerative colitis66.8% AI-predicted activityagainst MRSA7 registered studies
- Micafungin SodiumExisting use: Candidiasis66.8% AI-predicted activityagainst MRSA50+ registered studies
- AbemaciclibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 3 more66.4% AI-predicted activityagainst MRSA50+ registered studies
- RisperidoneExisting use: Aggressive behavior, Autism, Bipolar disorder and 4 more66.4% AI-predicted activityagainst MRSA50+ registered studies
- Lazertinib MesylateExisting use: Non-small cell lung carcinoma66.1% AI-predicted activityagainst MRSANo documented evidence found
- Desmopressin AcetateExisting use: Central diabetes insipidus, Diabetes insipidus, Enuresis and 5 more65.8% AI-predicted activityagainst MRSA50+ registered studies
- Terazosin HydrochlorideExisting use: Benign prostatic hyperplasia65.8% AI-predicted activityagainst MRSA41 registered studies
- VemurafenibExisting use: Cancer, Cutaneous melanoma, Melanoma and 2 more65.8% AI-predicted activityagainst MRSA50+ registered studies
- Caspofungin AcetateExisting use: Aspergillosis, Candidemia, Candidiasis and 1 more65.5% AI-predicted activityagainst MRSA50+ registered studies
- VenetoclaxExisting use: Cancer, Chronic lymphocytic leukemia, Neoplasm65.5% AI-predicted activityagainst MRSA50+ registered studies
- Larotrectinib SulfateExisting use: Abdominal Neoplasms, Cancer, Metastasis and 1 more65.4% AI-predicted activityagainst MRSA5 registered studies
- SirolimusExisting use: Adenoma sebaceum, Angiofibroma, Cancer and 5 more65.2% AI-predicted activityagainst MRSA50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
FOLFOX Chemotherapy Combined With Fruquintinib and Serplulimab as First-Line Conversion Therapy for Initially Unresectable pMMR/MSS Colorectal Cancer
NCT07446465 · start 2026-03-01
Registered record
- Registry ID
- NCT07446465
- Conditions
- Colorectal Cancer (Locally Advanced or Metastatic); Colorectal Cancer Microsatellite Stable (MSS)
- Interventions
- Serplulimab; Fruquintinib; mFOLFOX6 (oxaliplatin, calcium folinate, and 5-FU)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Not yet recruiting
- Start
- 2026-03-01
- Completion
- 2027-01-31
- Enrolment
- 42
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionColorectal Cancer (Locally Advanced or Metastatic); Colorectal Cancer Microsatellite Stable (MSS)InterventionSerplulimab; Fruquintinib; mFOLFOX6 (oxaliplatin, calcium folinate, and 5-FU)PhasePhase 4Registry statusNot yet recruitingStandard Second-line Therapy With ONgericimab and TOripalimab in pMMR/MSS Colorectal Cancer: a Single-arm Phase II Trial
NCT07106034 · start 2025-08-31
Registered record
- Registry ID
- NCT07106034
- Conditions
- Advanced Colorectal Cancer
- Interventions
- Ongericimab + Toripalimab + Bevacizumab + FOLFOX; Ongericimab + Toripalimab + Bevacizumab + FOLFIRI
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2025-08-31
- Completion
- 2028-07-31
- Enrolment
- 32
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAdvanced Colorectal CancerInterventionOngericimab + Toripalimab + Bevacizumab + FOLFOX; Ongericimab + Toripalimab + Bevacizumab + FOLFIRIPhasePhase 2Registry statusRecruitingIvonescimab in Combination With Liposomal Irinotecan and 5-FU/LV in Potentially Resectable Biliary Tract Malignancies
NCT06993025 · start 2025-05-25
Registered record
- Registry ID
- NCT06993025
- Conditions
- Biliary Tract Cancer
- Interventions
- Ivonescimab+chemotherapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2025-05-25
- Completion
- 2027-04-25
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBiliary Tract CancerInterventionIvonescimab+chemotherapyPhasePhase 2Registry statusNot yet recruitingLiposomal Irinotecan, 5-fluorouracil/Calcium Folinate, Oxaliplatin, and Adebrelimab in Combination With Radiotherapy for Resectable or Borderline Resectable Pancreatic Cancer With Risk Factors:A Prospective Exploratory Study
NCT07542002 · start 2025-03-25
Registered record
- Registry ID
- NCT07542002
- Conditions
- Pancreatic Cancer
- Interventions
- Irinotecan liposome, 5-fluorouracil/leucovorin, and oxaliplatin, with or without adadelimab.
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2025-03-25
- Completion
- 2026-05-31
- Enrolment
- 37
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPancreatic CancerInterventionIrinotecan liposome, 5-fluorouracil/leucovorin, and oxaliplatin, with or without adadelimab.PhasePhase 2Registry statusRecruitingA Study of Amivantamab and FOLFIRI Versus Cetuximab/Bevacizumab and FOLFIRI in Participants With KRAS/NRAS and BRAF Wild-type Colorectal Cancer Who Have Previously Received Chemotherapy
NCT06750094 · start 2024-12-12
Registered record
- Registry ID
- NCT06750094
- Conditions
- Colorectal Neoplasms
- Interventions
- Amivantamab; Cetuximab; Bevacizumab; 5-fluorouracil; Leucovorin calcium/Levoleucovorin; Irinotecan
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2024-12-12
- Completion
- 2029-04-13
- Enrolment
- 700
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionColorectal NeoplasmsInterventionAmivantamab; Cetuximab; Bevacizumab; 5-fluorouracil +2 morePhasePhase 3Registry statusRecruitingIrinotecan Liposome II in Combination With 5-FU/LV and Oxaliplatin in Perioperative Treatment of Borderline Resectable Pancreatic Cancer
NCT06387810 · start 2024-04-17
Registered record
- Registry ID
- NCT06387810
- Conditions
- Borderline Resectable Pancreatic Cancer
- Interventions
- irinotecan liposome II combined with 5-FU/LV and oxaliplatin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2024-04-17
- Completion
- 2026-06-30
- Enrolment
- 45
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBorderline Resectable Pancreatic CancerInterventionirinotecan liposome II combined with 5-FU/LV and oxaliplatinPhasePhase 2Registry statusUnknownTotal Neoadjuvant Treatment for pMMR Locally Advanced Low Rectal Cancer: Anti-PD-1 Antibody With FOLFOXIRI and Preoperative Radiation Therapy
NCT06099951 · start 2023-11-01
Registered record
- Registry ID
- NCT06099951
- Conditions
- Colorectal Cancer
- Interventions
- Serplulimab + FOLFOXIRI; Radiation therapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2023-11-01
- Completion
- 2027-09-01
- Enrolment
- 53
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionColorectal CancerInterventionSerplulimab + FOLFOXIRI; Radiation therapyPhasePhase 2Registry statusNot yet recruitingOrgan Preservation With Durvalumab-based Immunotherapy in Combination With Chemoradiation as Definitive Therapy for Early Stage Esophageal Adenocarcinoma With Indication for Radical Surgery
NCT05713838 · start 2023-08-28
Registered record
- Registry ID
- NCT05713838
- Conditions
- Esophagus Adenocarcinoma
- Interventions
- Durvalumab; FLOT; mFOLFOX-6; Radiotherapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Active not recruiting
- Start
- 2023-08-28
- Completion
- 2028-12
- Enrolment
- 32
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEsophagus AdenocarcinomaInterventionDurvalumab; FLOT; mFOLFOX-6; RadiotherapyPhasePhase 2Registry statusActive not recruitingA Phase II/III Study of HR070803 in Combination With Oxaliplatin, 5-fluorouracil, Calcium Folinate and Bevacizumab Versus FOLFOX in Combination With Bevacizumab for First-line Treatment of Advanced Colorectal Cancer
NCT05945901 · start 2023-08-14
Registered record
- Registry ID
- NCT05945901
- Conditions
- Colorectal Cancer
- Interventions
- HR070803 plus oxaliplatin, 5-FU/LV, bevacizumab; HR070803 simulator plus oxaliplatin, 5-FU/LV, bevacizumab
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Active not recruiting
- Start
- 2023-08-14
- Completion
- 2026-12-01
- Enrolment
- 669
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionColorectal CancerInterventionHR070803 plus oxaliplatin, 5-FU/LV, bevacizumab; HR070803 simulator plus oxaliplatin, 5-FU/LV, bevacizumabPhasePhase 2 / Phase 3Registry statusActive not recruitingVenetoclax Basket Trial for High Risk Hematologic Malignancies
NCT05292664 · start 2023-03-29
Registered record
- Registry ID
- NCT05292664
- Conditions
- Myelodysplastic Syndromes, de Novo; Myelodysplastic Syndromes, Secondary; Myelodysplastic Syndromes, Previously Treated; Treatment-Related Acute Myeloid Leukemia; Therapy-Related Myelodysplastic Syndrome; Acute Lymphoblastic Leukemia, in Relapse; Acute Lymphoblastic Leukemia With Failed Remission; Lymphoblastic Lymphoma, in Relapse; Lymphoblastic Lymphoma, Refractory; Acute Leukemia of Ambiguous Lineage in Relapse; Acute Leukemia of Ambiguous Lineage
- Interventions
- Venetoclax; Azacitidine; Cytarabine; Methotrexate; Hydrocortisone; Leucovorin; Dexamethasone; Vincristine; Doxorubicin; Dexrazoxane; Calaspargase Pegol; Erwinia asparaginase
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Recruiting
- Start
- 2023-03-29
- Completion
- 2030-07-02
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMyelodysplastic Syndromes, de Novo; Myelodysplastic Syndromes, Secondary; Myelodysplastic Syndromes, Previously Treated; Treatment-Related Acute Myeloid Leukemia +7 moreInterventionVenetoclax; Azacitidine; Cytarabine; Methotrexate +8 morePhasePhase 1Registry statusRecruitingComparing the Safety and Efficacy of First-line Polychemotherapy and Polychemotherapy in Combination With PIPAC Sessions
NCT06313801 · start 2023-01-19
Registered record
- Registry ID
- NCT06313801
- Conditions
- Gastric Cancer
- Interventions
- Docetaxel; Oxaliplatin; Calcium folinate; Fluorouracil; Diagnostic laparoscopy; dPIPAC ( The description of the standard diagnostic laparoscopy procedure and the session of PIPAC (dPIPAC)).
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2023-01-19
- Completion
- 2027-09-01
- Enrolment
- 106
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGastric CancerInterventionDocetaxel; Oxaliplatin; Calcium folinate; Fluorouracil +2 morePhasePhase 2Registry statusRecruitingClinical Trial of Apatinib Reverses Chemotherapy-Resistance of Patients With Advanced Gastric Cancer
NCT02697838 · start 2016-08-01
Registered record
- Registry ID
- NCT02697838
- Conditions
- Malignant Neoplasm of Stomach Stage II
- Interventions
- Apatinib; Paclitaxel-based chemotherapeutic regimens
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2016-08-01
- Completion
- 2018-10-31
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMalignant Neoplasm of Stomach Stage IIInterventionApatinib; Paclitaxel-based chemotherapeutic regimensPhasePhase 2Registry statusUnknownCarfilzomib and Hyper-CVAD in Treating Patients With Newly Diagnosed Acute Lymphoblastic Leukemia or Lymphoma
NCT02293109 · start 2015-12-17
Registered record
- Registry ID
- NCT02293109
- Conditions
- Contiguous Stage II Adult Lymphoblastic Lymphoma; Noncontiguous Stage II Adult Lymphoblastic Lymphoma; Stage I Adult Lymphoblastic Lymphoma; Stage III Adult Lymphoblastic Lymphoma; Stage IV Adult Lymphoblastic Lymphoma; Untreated Adult Acute Lymphoblastic Leukemia
- Interventions
- carfilzomib; cyclophosphamide; vincristine sulfate; doxorubicin hydrochloride; dexamethasone; methotrexate; cytarabine; leucovorin calcium; methylprednisolone; rituximab; laboratory biomarker analysis
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2015-12-17
- Completion
- 2018-01-11
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionContiguous Stage II Adult Lymphoblastic Lymphoma; Noncontiguous Stage II Adult Lymphoblastic Lymphoma; Stage I Adult Lymphoblastic Lymphoma; Stage III Adult Lymphoblastic Lymphoma +2 moreInterventioncarfilzomib; cyclophosphamide; vincristine sulfate; doxorubicin hydrochloride +7 morePhasePhase 1Registry statusCompletedSafety and Efficacy of Modified Folfirinox Versus Gemcis in Bile Duct Tumours
NCT02591030 · start 2015-12-15
Registered record
- Registry ID
- NCT02591030
- Conditions
- Bile Duct Cancer
- Interventions
- GEMCIS; mFolfirinox
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Completed
- Start
- 2015-12-15
- Completion
- 2020-01-16
- Enrolment
- 191
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBile Duct CancerInterventionGEMCIS; mFolfirinoxPhasePhase 2 / Phase 3Registry statusCompletedCombination Chemotherapy With or Without Blinatumomab in Treating Patients With Newly Diagnosed BCR-ABL-Negative B Lineage Acute Lymphoblastic Leukemia
NCT02003222 · start 2014-05-19
Registered record
- Registry ID
- NCT02003222
- Conditions
- Acute Lymphoblastic Leukemia; B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative
- Interventions
- Allogeneic Hematopoietic Stem Cell Transplantation; Biospecimen Collection; Blinatumomab; Bone Marrow Aspiration; Bone Marrow Biopsy; Cyclophosphamide; Cytarabine; Daunorubicin; Daunorubicin Hydrochloride; Dexamethasone; Etoposide; Leucovorin Calcium; Lumbar Puncture; Mercaptopurine; Methotrexate; Pegaspargase; Prednisone; Rituximab; Vincristine; Vincristine Sulfate; X-Ray Imaging
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Active not recruiting
- Start
- 2014-05-19
- Completion
- 2027-02-25
- Enrolment
- 488
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Lymphoblastic Leukemia; B Acute Lymphoblastic Leukemia, Philadelphia Chromosome NegativeInterventionAllogeneic Hematopoietic Stem Cell Transplantation; Biospecimen Collection; Blinatumomab; Bone Marrow Aspiration +17 morePhasePhase 3Registry statusActive not recruiting