Venetoclax
FDA-approved product (tablet, oral), marketed as Venclexta, Venetoclax.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Cancer
- Chronic lymphocytic leukemia
- Neoplasm
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Other antineoplastic agents
- FDA pharmacologic class
- BCL-2 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 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- MRSA65.5% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli55.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae45.9% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- M. tuberculosis67.5% 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 Venetoclax 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.
- UrsodiolExisting use: Biliary liver cirrhosis, Primary biliary cirrhosis69.2% AI-predicted activityagainst MRSA50+ registered studies
- OlaparibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 9 more69.2% AI-predicted activityagainst MRSA50+ registered studies
- Ganirelix AcetateExisting use: Female infertility, Positive regulation of ovulation, Reproductive Techniques, Assisted69.1% AI-predicted activityagainst MRSA50+ registered studies
- DanicopanExisting use: Acquired paroxysmal nocturnal hemoglobinuria, Hemoglobinuria, Paroxysmal, Hemolysis68.7% AI-predicted activityagainst MRSA30 registered studies
- Simeprevir SodiumExisting use: Chronic hepatitis C virus infection68.6% AI-predicted activityagainst MRSANo documented evidence found
- Lanreotide AcetateExisting use: Acromegaly, Carcinoid syndrome68.3% AI-predicted activityagainst MRSA50+ registered studies
- Cholic AcidExisting use: Abnormality of the gastrointestinal tract, Inborn errors of metabolism, Liver disease and 1 more68.0% AI-predicted activityagainst MRSA50+ registered studies
- EptifibatideExisting use: Acute coronary syndrome, Acute myocardial infarction, Intermediate coronary syndrome and 2 more67.8% AI-predicted activityagainst MRSA35 registered studies
- AbarelixExisting use: Neoplasm67.7% AI-predicted activityagainst MRSA5 registered studies
- EverolimusExisting use: Adenoma sebaceum, Anaplastic astrocytoma, Angiomyolipoma and 18 more67.5% AI-predicted activityagainst MRSA50+ registered studies
- Paliperidone PalmitateExisting use: Mental or behavioural disorder, Psychosis, Schizoaffective disorder and 1 more67.3% AI-predicted activityagainst MRSA50+ registered studies
- PaliperidoneExisting use: Mental or behavioural disorder, Psychosis, Schizoaffective disorder and 1 more67.2% AI-predicted activityagainst MRSA50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Tafasitamab With Acalabrutinib and Venetoclax for the Treatment of Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
NCT07582159 · start 2026-12-19
Registered record
- Registry ID
- NCT07582159
- Conditions
- Chronic Lymphocytic Leukemia; Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma; Small Lymphocytic Lymphoma
- Interventions
- Acalabrutinib; Biospecimen Collection; Bone Marrow Biopsy; Computed Tomography; Positron Emission Tomography; Tafasitamab; Venetoclax
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-12-19
- Completion
- 2029-04-14
- Enrolment
- 35
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Lymphocytic Leukemia; Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma; Small Lymphocytic LymphomaInterventionAcalabrutinib; Biospecimen Collection; Bone Marrow Biopsy; Computed Tomography +3 morePhasePhase 2Registry statusNot yet recruitingLiposomal Mitoxantrone Plus Azacitidine and Venetoclax in Newly Diagnosed Elderly or Unfit AML
NCT07828535 · start 2026-10-30
Registered record
- Registry ID
- NCT07828535
- Conditions
- Acute Myeloid Leukemia (AML)
- Interventions
- Liposome Mitoxantrone; Venetoclax; Azacitidine
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Not yet recruiting
- Start
- 2026-10-30
- Completion
- 2032-12-31
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Myeloid Leukemia (AML)InterventionLiposome Mitoxantrone; Venetoclax; AzacitidinePhasePhase 1Registry statusNot yet recruitingVenetoclax Plus Zanubrutinib for the Treatment of Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
NCT07734038 · start 2026-10-01
Registered record
- Registry ID
- NCT07734038
- Conditions
- Chronic Lymphocytic Leukemia; Small Lymphocytic Lymphoma
- Interventions
- Biospecimen Collection; Bone Marrow Aspiration; Bone Marrow Biopsy; Computed Tomography; Magnetic Resonance Imaging; Venetoclax; Zanubrutinib
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2026-10-01
- Completion
- 2027-12-31
- Enrolment
- 155
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Lymphocytic Leukemia; Small Lymphocytic LymphomaInterventionBiospecimen Collection; Bone Marrow Aspiration; Bone Marrow Biopsy; Computed Tomography +3 morePhasePhase 2Registry statusRecruitingA Study of Azacitidine and Venetoclax Versus a Stem Cell Transplant in People 65 Years and Older With Acute Myeloid Leukemia
NCT06903702 · start 2026-08-04
Registered record
- Registry ID
- NCT06903702
- Conditions
- Acute Myeloid Leukemia
- Interventions
- Azacitidine (AZA); Venetoclax; Allogeneic hematopoietic stem cell transplantation
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Withdrawn
- Start
- 2026-08-04
- Completion
- 2027-06
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Myeloid LeukemiaInterventionAzacitidine (AZA); Venetoclax; Allogeneic hematopoietic stem cell transplantationPhasePhase 2Registry statusWithdrawnReassessment of the Risk of Hemolytic Syndrome in Patients With Chronic Lymphocytic Leukemia Treated With a Regimen Containing Venetoclax
NCT07691047 · start 2026-07-31
Registered record
- Registry ID
- NCT07691047
- Conditions
- Chronic Lymphoid Leukemia
- Interventions
- Cervical, Thoracic, Abdominal, and Pelvic CT Scan
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Not yet recruiting
- Start
- 2026-07-31
- Completion
- 2029-09-30
- Enrolment
- 130
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Lymphoid LeukemiaInterventionCervical, Thoracic, Abdominal, and Pelvic CT ScanPhaseNot applicableRegistry statusNot yet recruitingTesting the Use of Combination Therapy in Patients With Persistent Low Level Acute Myeloid Leukemia Following Initial Treatment, The ERASE Study (A MyeloMATCH Treatment Trial)
NCT05554419 · start 2026-07-01
Registered record
- Registry ID
- NCT05554419
- Conditions
- Acute Myeloid Leukemia; Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome; Acute Myeloid Leukemia Arising From Previous Myeloproliferative Neoplasm; Acute Myeloid Leukemia Post Cytotoxic Therapy; Secondary Acute Myeloid Leukemia
- Interventions
- Azacitidine; Bone Marrow Aspiration and Biopsy; Cytarabine; Echocardiography Test; Liposome-encapsulated Daunorubicin-Cytarabine; Multigated Acquisition Scan; Venetoclax
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-07-01
- Completion
- 2026-08-31
- Enrolment
- 184
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Myeloid Leukemia; Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome; Acute Myeloid Leukemia Arising From Previous Myeloproliferative Neoplasm; Acute Myeloid Leukemia Post Cytotoxic Therapy +1 moreInterventionAzacitidine; Bone Marrow Aspiration and Biopsy; Cytarabine; Echocardiography Test +3 morePhasePhase 2Registry statusNot yet recruitingStudy on the Efficacy and Safety of VA Regimen Compared to "3+7" Regimen in Newly Diagnosed AML With NPM1 or IDH1/IDH2 Mutations
NCT07664839 · start 2026-07-01
Registered record
- Registry ID
- NCT07664839
- Conditions
- Acute Myeloid Leukemia; NPM1 Mutation; IDH1 Mutation; IDH2 Mutation
- Interventions
- VEN combined with azacitidine; Cytarabine plus Daunorubicin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-07-01
- Completion
- 2032-05-31
- Enrolment
- 148
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Myeloid Leukemia; NPM1 Mutation; IDH1 Mutation; IDH2 MutationInterventionVEN combined with azacitidine; Cytarabine plus DaunorubicinPhasePhase 2Registry statusNot yet recruitingSalvage Haploidentical HSCT With DLI and Targeted Therapy for R/R AML
NCT07572695 · start 2026-04-30
Registered record
- Registry ID
- NCT07572695
- Conditions
- Acute Myeloid Leukemia; Relapsed/Refractory Acute Myeloid Leukemia; AML, Relapsed/Refractory
- Interventions
- Haploidentical Allogeneic Hematopoietic Stem Cell Transplantation (haplo-HSCT); Post-transplant Maintenance Therapy
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Not yet recruiting
- Start
- 2026-04-30
- Completion
- 2028-12
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Myeloid Leukemia; Relapsed/Refractory Acute Myeloid Leukemia; AML, Relapsed/RefractoryInterventionHaploidentical Allogeneic Hematopoietic Stem Cell Transplantation (haplo-HSCT); Post-transplant Maintenance TherapyPhaseNot recordedRegistry statusNot yet recruitingCApivasertib, Venetoclax And Low-intensity chemotheRapY for Adults With ALL/LBL
NCT07294677 · start 2026-03-17
Registered record
- Registry ID
- NCT07294677
- Conditions
- Leukemia; Lymphoma
- Interventions
- Capivasertib; Venetoclax; Rituximab; Blinatumomab; Nelarabine; mini-hyperCVD
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Recruiting
- Start
- 2026-03-17
- Completion
- 2032-03
- Enrolment
- 104
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLeukemia; LymphomaInterventionCapivasertib; Venetoclax; Rituximab; Blinatumomab +2 morePhasePhase 1 / Phase 2Registry statusRecruitingVenetoclax, Azacitidine, and Mitoxantrone Hydrochloride Liposome Versus Idarubicin and Cytarabine in Newly Diagnosed AML
NCT07486479 · start 2026-03-10
Registered record
- Registry ID
- NCT07486479
- Conditions
- Acute Myeloid Leukemia (AML)
- Interventions
- Mitoxantrone Hydrochloride Liposome; Venetoclax; Azacitidine; Idarubicin; Cytarabine
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Not yet recruiting
- Start
- 2026-03-10
- Completion
- 2027-12-31
- Enrolment
- 204
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Myeloid Leukemia (AML)InterventionMitoxantrone Hydrochloride Liposome; Venetoclax; Azacitidine; Idarubicin +1 morePhasePhase 3Registry statusNot yet recruitingA Study to Investigate Sonrotoclax (BGB-11417) Plus Zanubrutinib (BGB-3111) Compared With Venetoclax Plus Acalabrutinib in Adults With Previously Untreated Chronic Lymphocytic Leukemia
NCT07277231 · start 2026-01-22
Registered record
- Registry ID
- NCT07277231
- Conditions
- Chronic Lymphocytic Leukemia
- Interventions
- Sonrotoclax; Zanubrutinib; Acalabrutinib; Venetoclax
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2026-01-22
- Completion
- 2031-11
- Enrolment
- 500
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Lymphocytic LeukemiaInterventionSonrotoclax; Zanubrutinib; Acalabrutinib; VenetoclaxPhasePhase 3Registry statusRecruitingPre-DLI or Pro-DLI in Relapsed/Refractory Myeloid Neoplasms After HSCT
NCT07319793 · start 2026-01-01
Registered record
- Registry ID
- NCT07319793
- Conditions
- Acute Myeloid Leukemia; Myelodysplastic Syndromes (MDS)
- Interventions
- Prophylactic DLI; Preemptive DLI
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Not yet recruiting
- Start
- 2026-01-01
- Completion
- 2028-06-30
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Myeloid Leukemia; Myelodysplastic Syndromes (MDS)InterventionProphylactic DLI; Preemptive DLIPhaseNot applicableRegistry statusNot yet recruitingVenetoclax-Enhanced BUCY vs. Standard BUCY Conditioning in High-Risk AML and MDS Patients Undergoing Allo-HSCT (Ven-BUCY Study)
NCT07183878 · start 2025-08-20
Registered record
- Registry ID
- NCT07183878
- Conditions
- Acute Myeloid Leukemia; High-Risk Acute Myeloid Leukemia; Myelodysplastic Syndromes; High-Risk Myelodysplastic Syndromes
- Interventions
- Venetoclax; None-placebo; Busulfan (BU)
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2025-08-20
- Completion
- 2028-08-20
- Enrolment
- 138
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Myeloid Leukemia; High-Risk Acute Myeloid Leukemia; Myelodysplastic Syndromes; High-Risk Myelodysplastic SyndromesInterventionVenetoclax; None-placebo; Busulfan (BU)PhaseNot applicableRegistry statusRecruitingComparing New Treatments for People With Newly Diagnosed Acute Myeloid Leukemia That Has an IDH2 Gene Change (A MyeloMATCH Treatment Trial)
NCT06672146 · start 2025-05-16
Registered record
- Registry ID
- NCT06672146
- Conditions
- Acute Myeloid Leukemia
- Interventions
- Biospecimen Collection; Bone Marrow Aspiration; Bone Marrow Biopsy; Decitabine and Cedazuridine; Enasidenib; Venetoclax
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2025-05-16
- Completion
- 2027-03-31
- Enrolment
- 93
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Myeloid LeukemiaInterventionBiospecimen Collection; Bone Marrow Aspiration; Bone Marrow Biopsy; Decitabine and Cedazuridine +2 morePhasePhase 2Registry statusRecruitingNewly-diagnosed Pediatric Ph-positive B-ALL Protocol
NCT07152041 · start 2025-03-28
Registered record
- Registry ID
- NCT07152041
- Conditions
- Acute Lymphoblastic Leukemia (ALL) Philadelphia Chromosome-positive (Ph+); Childhood Leukemia, Acute Lymphoblastic
- Interventions
- olverembatinib
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2025-03-28
- Completion
- 2030-06
- Enrolment
- 150
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Lymphoblastic Leukemia (ALL) Philadelphia Chromosome-positive (Ph+); Childhood Leukemia, Acute LymphoblasticInterventionolverembatinibPhasePhase 3Registry statusRecruiting