Romidepsin
FDA-approved product (powder, intravenous), marketed as Istodax, Romidepsin.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Cancer
- Cutaneous T-cell lymphoma
- Mature T-cell and NK-cell non-Hodgkin lymphoma
- Neoplasm
- T-cell non-Hodgkin lymphoma
- Unspecified peripheral T-cell lymphoma
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Histone deacetylase (hdac) inhibitors
- FDA pharmacologic class
- Histone Deacetylase 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 and MRSA. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA52.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli35.3% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae38.2% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis50.8% 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 measuredAutoDock 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 Romidepsin 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.
Romidepsin in Combination With Lenalidomide in Adults With Relapsed or Refractory Lymphomas and Myeloma
NCT01755975 · start 2012-12
Registered record
- Registry ID
- NCT01755975
- Conditions
- Multiple Myeloma; Non-Hodgkin's Lymphoma
- Interventions
- Romidepsin; Lenalidomide
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Completed
- Start
- 2012-12
- Completion
- 2023-10
- Enrolment
- 49
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMultiple Myeloma; Non-Hodgkin's LymphomaInterventionRomidepsin; LenalidomidePhasePhase 1 / Phase 2Registry statusCompletedRomidepsin, Ifosfamide, Carboplatin, and Etoposide in Treating Participants With Relapsed or Refractory Peripheral T-Cell Lymphoma
NCT01590732 · start 2012-10-29
Registered record
- Registry ID
- NCT01590732
- Conditions
- Mycosis Fungoides; Recurrent Anaplastic Large Cell Lymphoma; Recurrent Angioimmunoblastic T-Cell Lymphoma; Recurrent Enteropathy-Associated T-Cell Lymphoma; Recurrent Hepatosplenic T-Cell Lymphoma; Recurrent Peripheral T-Cell Lymphoma, Not Otherwise Specified; Refractory Anaplastic Large Cell Lymphoma; Refractory Angioimmunoblastic T-Cell Lymphoma; Refractory Enteropathy-Associated T-Cell Lymphoma; Refractory Hepatosplenic T-Cell Lymphoma; Refractory Peripheral T-Cell Lymphoma, Not Otherwise Specified
- Interventions
- Carboplatin; Etoposide; Ifosfamide; Romidepsin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2012-10-29
- Completion
- 2018-05-02
- Enrolment
- 22
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMycosis Fungoides; Recurrent Anaplastic Large Cell Lymphoma; Recurrent Angioimmunoblastic T-Cell Lymphoma; Recurrent Enteropathy-Associated T-Cell Lymphoma +7 moreInterventionCarboplatin; Etoposide; Ifosfamide; RomidepsinPhasePhase 1Registry statusCompletedA Trial of Oral 5-azacitidine in Combination With Romidepsin in Advanced Solid Tumors, With an Expansion Cohort in Virally Mediated Cancers and Liposarcoma
NCT01537744 · start 2012-02
Registered record
- Registry ID
- NCT01537744
- Conditions
- Solid Tumors; Virally Mediated Cancers and Liposarcoma
- Interventions
- oral 5-azacitidine in combination with romidepsin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2012-02
- Completion
- 2016-09
- Enrolment
- 18
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSolid Tumors; Virally Mediated Cancers and LiposarcomaInterventionoral 5-azacitidine in combination with romidepsinPhasePhase 1Registry statusCompletedInfluence of Ketoconazole on the Pharmacokinetics of Romidepsin in Patients With Advanced Cancer
NCT01324310 · start 2011-04-01
Registered record
- Registry ID
- NCT01324310
- Conditions
- Hematologic Malignancy; Malignant Lymphoma
- Interventions
- Romidepsin; Ketoconazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2011-04-01
- Completion
- 2012-01-01
- Enrolment
- 15
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHematologic Malignancy; Malignant LymphomaInterventionRomidepsin; KetoconazolePhasePhase 1Registry statusCompletedA Study of Escalating Doses of Romidepsin in Association With CHOP in the Treatment of Peripheral T-Cell Lymphomas
NCT01280526 · start 2011-01
Registered record
- Registry ID
- NCT01280526
- Conditions
- Peripheral T Cell Lymphoma
- Interventions
- Romidepsin and CHOP; Romidepsin and CHOP; Romidepsin and CHOP; Romidepsin and CHOP
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Completed
- Start
- 2011-01
- Completion
- 2014-03
- Enrolment
- 37
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPeripheral T Cell LymphomaInterventionRomidepsin and CHOP; Romidepsin and CHOP; Romidepsin and CHOP; Romidepsin and CHOPPhasePhase 1 / Phase 2Registry statusCompletedTopical Romidepsin to Treat Early-Stage Cutaneous T-Cell Lymphoma
NCT01445340 · start 2007-04-21
Registered record
- Registry ID
- NCT01445340
- Conditions
- Mycosis Fungoides; Cutaneous T-Cell Lymphoma; Neoplasms
- Interventions
- Romidepsin (FR901228)
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Terminated
- Start
- 2007-04-21
- Completion
- 2012-06-29
- Enrolment
- 6
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMycosis Fungoides; Cutaneous T-Cell Lymphoma; NeoplasmsInterventionRomidepsin (FR901228)PhasePhase 1Registry statusTerminatedA Phase I/II Trial of Romidepsin (Depsipeptide) and Bortezomib in Patients With Relapsed Myeloma
NCT00431990 · start 2006-11
Registered record
- Registry ID
- NCT00431990
- Conditions
- Multiple Myeloma
- Interventions
- depsipeptide; bortezomib; dexamethasone
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Unknown
- Start
- 2006-11
- Completion
- 2012-01
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMultiple MyelomaInterventiondepsipeptide; bortezomib; dexamethasonePhasePhase 1 / Phase 2Registry statusUnknownDepsipeptide in Unresectable Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck
NCT00084682 · start 2005-06
Registered record
- Registry ID
- NCT00084682
- Conditions
- Stage IV Squamous Cell Carcinoma of the Hypopharynx; Stage IV Squamous Cell Carcinoma of the Larynx; Stage IV Squamous Cell Carcinoma of the Lip and Oral Cavity; Stage IV Squamous Cell Carcinoma of the Oropharynx
- Interventions
- romidepsin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2005-06
- Completion
- 2012-03
- Enrolment
- 14
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionStage IV Squamous Cell Carcinoma of the Hypopharynx; Stage IV Squamous Cell Carcinoma of the Larynx; Stage IV Squamous Cell Carcinoma of the Lip and Oral Cavity; Stage IV Squamous Cell Carcinoma of the OropharynxInterventionromidepsinPhasePhase 2Registry statusCompletedFR901228 in Treating Patients With Relapsed or Refractory Advanced Ovarian Epithelial Cancer
NCT00085527 · start 2005-05
Registered record
- Registry ID
- NCT00085527
- Conditions
- Ovarian Cancer
- Interventions
- depsipeptide
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Withdrawn
- Start
- 2005-05
- Completion
- 2005-09
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOvarian CancerInterventiondepsipeptidePhasePhase 2Registry statusWithdrawnFR901228 in Treating Patients With Metastatic Breast Cancer
NCT00098397 · start 2005-02
Registered record
- Registry ID
- NCT00098397
- Conditions
- Male Breast Cancer; Recurrent Breast Cancer; Stage IV Breast Cancer
- Interventions
- romidepsin; laboratory biomarker analysis
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2005-02
- Completion
- Not recorded
- Enrolment
- 37
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMale Breast Cancer; Recurrent Breast Cancer; Stage IV Breast CancerInterventionromidepsin; laboratory biomarker analysisPhasePhase 2Registry statusCompletedDepsipeptide (Romidepsin) in Treating Patients With Metastatic or Unresectable Soft Tissue Sarcoma
NCT00112463 · start 2005-01-07
Registered record
- Registry ID
- NCT00112463
- Conditions
- Adult Alveolar Soft-part Sarcoma; Adult Angiosarcoma; Adult Epithelioid Sarcoma; Adult Extraskeletal Chondrosarcoma; Adult Extraskeletal Osteosarcoma; Adult Fibrosarcoma; Adult Leiomyosarcoma; Adult Liposarcoma; Adult Malignant Fibrous Histiocytoma; Adult Malignant Hemangiopericytoma; Adult Malignant Mesenchymoma; Adult Neurofibrosarcoma; Adult Rhabdomyosarcoma; Adult Synovial Sarcoma; Gastrointestinal Stromal Tumor; Metastatic Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor; Recurrent Adult Soft Tissue Sarcoma; Recurrent Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor; Stage III Adult Soft Tissue Sarcoma; Stage IV Adult Soft Tissue Sarcoma
- Interventions
- romidepsin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2005-01-07
- Completion
- 2008-10-23
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAdult Alveolar Soft-part Sarcoma; Adult Angiosarcoma; Adult Epithelioid Sarcoma; Adult Extraskeletal Chondrosarcoma +16 moreInterventionromidepsinPhasePhase 2Registry statusCompletedFR901228 in Treating Patients With Recurrent High-Grade Gliomas
NCT00085540 · start 2005-01
Registered record
- Registry ID
- NCT00085540
- Conditions
- Adult Anaplastic Astrocytoma; Adult Anaplastic Oligodendroglioma; Adult Giant Cell Glioblastoma; Adult Gliosarcoma; Recurrent Adult Brain Tumor
- Interventions
- depsipeptide
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Completed
- Start
- 2005-01
- Completion
- 2009-03
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAdult Anaplastic Astrocytoma; Adult Anaplastic Oligodendroglioma; Adult Giant Cell Glioblastoma; Adult Gliosarcoma +1 moreInterventiondepsipeptidePhasePhase 1 / Phase 2Registry statusCompletedDepsipeptide/Flavopiridol Infusion for Cancers of the Lungs, Esophagus, Pleura, Thymus or Mediastinum
NCT00094978 · start 2004-10-25
Registered record
- Registry ID
- NCT00094978
- Conditions
- Carcinoma, Small Cell; Carcinoma, Non-Small-Cell Lung; Esophageal Neoplasms; Mesothelioma
- Interventions
- Depsipeptide; Flavopiridol (alvocidib)
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Terminated
- Start
- 2004-10-25
- Completion
- 2013-05-20
- Enrolment
- 23
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCarcinoma, Small Cell; Carcinoma, Non-Small-Cell Lung; Esophageal Neoplasms; MesotheliomaInterventionDepsipeptide; Flavopiridol (alvocidib)PhasePhase 1Registry statusTerminatedA Research Study for Patients With Prostate Cancer
NCT00106418 · start 2003-05-07
Registered record
- Registry ID
- NCT00106418
- Conditions
- Prostate Cancer; Metastases
- Interventions
- Romidepsin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2003-05-07
- Completion
- 2006-09-01
- Enrolment
- 35
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionProstate Cancer; MetastasesInterventionRomidepsinPhasePhase 2Registry statusCompletedRomidepsin in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia
NCT00062075 · start 2003-05
Registered record
- Registry ID
- NCT00062075
- Conditions
- Adult Acute Myeloid Leukemia With 11q23 (MLL) Abnormalities; Adult Acute Myeloid Leukemia With Del(5q); Adult Acute Myeloid Leukemia With Inv(16)(p13; q22); Adult Acute Myeloid Leukemia With t(15; 17)(q22; q12); Adult Acute Myeloid Leukemia With t(16; 16)(p13; q22); Adult Acute Myeloid Leukemia With t(8; 21)(q22; q22); Adult Acute Promyelocytic Leukemia (M3); Recurrent Adult Acute Myeloid Leukemia
- Interventions
- romidepsin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2003-05
- Completion
- Not recorded
- Enrolment
- 47
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAdult Acute Myeloid Leukemia With 11q23 (MLL) Abnormalities; Adult Acute Myeloid Leukemia With Del(5q); Adult Acute Myeloid Leukemia With Inv(16)(p13; q22) +11 moreInterventionromidepsinPhasePhase 2Registry statusCompleted