Danicopan
FDA-approved product (tablet, oral), marketed as Voydeya.
- Registered studies
- 30
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Acquired paroxysmal nocturnal hemoglobinuria
- Hemoglobinuria, Paroxysmal
- Hemolysis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Complement inhibitors
- FDA pharmacologic class
- Complement Factor D 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 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- MRSA68.7% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli46.9% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae29.9% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis53.4% 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
30registered studies name this medicine, for any condition. See them below.
Experimental
No evidence found
No laboratory measurement against the four pathogens in the ChEMBL records loaded here.
Docking
Computational · nothing measuredEnoyl-ACP reductase (InhA) ↗ (M. tuberculosis)
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 Danicopan 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
- 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
- Ozanimod HydrochlorideExisting use: Multiple sclerosis, Relapsing-remitting multiple sclerosis, Ulcerative colitis66.8% AI-predicted activityagainst MRSA7 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
A Proof of Concept Study for a 12 Month Treatment in Patients With C3G or IC-MPGN Treated With ACH-0144471
NCT03459443 · start 2018-06-20
Registered record
- Registry ID
- NCT03459443
- Conditions
- C3 Glomerulonephritis; C3 Glomerulopathy; Immune Complex Membranoproliferative Glomerulonephritis; IC-MPGN; Dense Deposit Disease
- Interventions
- Danicopan
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2018-06-20
- Completion
- 2021-03-29
- Enrolment
- 22
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionC3 Glomerulonephritis; C3 Glomerulopathy; Immune Complex Membranoproliferative Glomerulonephritis; IC-MPGN +1 moreInterventionDanicopanPhasePhase 2Registry statusTerminatedA Proof-of-Concept Study of Danicopan for 6 Months of Treatment in Participants With C3 Glomerulopathy (C3G)
NCT03369236 · start 2018-06-12
Registered record
- Registry ID
- NCT03369236
- Conditions
- C3 Glomerulopathy; C3 Glomerulonephritis; Dense Deposit Disease
- Interventions
- Danicopan; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2018-06-12
- Completion
- 2020-12-18
- Enrolment
- 13
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionC3 Glomerulopathy; C3 Glomerulonephritis; Dense Deposit DiseaseInterventionDanicopan; PlaceboPhasePhase 2Registry statusCompletedStudy of Danicopan in Participants With Paroxysmal Nocturnal Hemoglobinuria With Inadequate Response to Eculizumab
NCT03472885 · start 2018-05-08
Registered record
- Registry ID
- NCT03472885
- Conditions
- Paroxysmal Nocturnal Hemoglobinuria (PNH)
- Interventions
- Danicopan; Eculizumab
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2018-05-08
- Completion
- 2023-01-05
- Enrolment
- 12
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionParoxysmal Nocturnal Hemoglobinuria (PNH)InterventionDanicopan; EculizumabPhasePhase 2Registry statusCompletedStudy of Danicopan in Participants With Hepatic Impairment
NCT03555539 · start 2018-05-01
Registered record
- Registry ID
- NCT03555539
- Conditions
- Hepatic Impairment
- Interventions
- Danicopan
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2018-05-01
- Completion
- 2018-09-21
- Enrolment
- 16
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatic ImpairmentInterventionDanicopanPhasePhase 1Registry statusCompletedStudy of Danicopan in Participants With Normal Kidney Function and Participants With Kidney Dysfunction
NCT04935294 · start 2018-01-24
Registered record
- Registry ID
- NCT04935294
- Conditions
- Healthy; Renal Dysfunction
- Interventions
- Danicopan
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2018-01-24
- Completion
- 2018-05-29
- Enrolment
- 16
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy; Renal DysfunctionInterventionDanicopanPhasePhase 1Registry statusCompletedA Study of Modified Release Formulations of Danicopan in Healthy Adult Participants
NCT03384186 · start 2017-12-01
Registered record
- Registry ID
- NCT03384186
- Conditions
- Healthy
- Interventions
- Danicopan Modified Release Prototype 1; Danicopan Modified Release Prototype 2; Danicopan Modified Release Prototype 3
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2017-12-01
- Completion
- 2018-03-21
- Enrolment
- 14
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionDanicopan Modified Release Prototype 1; Danicopan Modified Release Prototype 2; Danicopan Modified Release Prototype 3PhasePhase 1Registry statusCompletedStudy of Radiolabeled Danicopan in Healthy Male Participants
NCT04889391 · start 2017-09-14
Registered record
- Registry ID
- NCT04889391
- Conditions
- Healthy
- Interventions
- [14C]-Danicopan
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2017-09-14
- Completion
- 2017-10-15
- Enrolment
- 8
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyIntervention[14C]-DanicopanPhasePhase 1Registry statusCompletedA Proof-of-Mechanism Study to Determine the Effect of Danicopan on C3 Levels in Participants With C3G or IC-MPGN
NCT03124368 · start 2017-08-09
Registered record
- Registry ID
- NCT03124368
- Conditions
- C3 Glomerulonephritis; Dense Deposit Disease; C3 Glomerulopathy; Immune Complex Mediated Membranoproliferative Glomerulonephritis; Membranoproliferative Glomerulonephritis Types I, II, and III
- Interventions
- Danicopan
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2017-08-09
- Completion
- 2019-01-09
- Enrolment
- 6
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionC3 Glomerulonephritis; Dense Deposit Disease; C3 Glomerulopathy; Immune Complex Mediated Membranoproliferative Glomerulonephritis +1 moreInterventionDanicopanPhasePhase 2Registry statusCompletedA Long-Term Treatment Study of ACH-0144471 in Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH)
NCT03181633 · start 2017-06-22
Registered record
- Registry ID
- NCT03181633
- Conditions
- Paroxysmal Nocturnal Hemoglobinuria
- Interventions
- ACH-0144471
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2017-06-22
- Completion
- 2022-01-04
- Enrolment
- 8
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionParoxysmal Nocturnal HemoglobinuriaInterventionACH-0144471PhasePhase 2Registry statusCompletedA Drug Interaction Study Between Danicopan and Midazolam, Fexofenadine, and Mycophenolate Mofetil in Healthy Participants
NCT03108274 · start 2017-04-18
Registered record
- Registry ID
- NCT03108274
- Conditions
- Healthy
- Interventions
- Danicopan; Midazolam; Fexofenadine; Mycophenolate Mofetil
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2017-04-18
- Completion
- 2017-06-16
- Enrolment
- 35
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionDanicopan; Midazolam; Fexofenadine; Mycophenolate MofetilPhasePhase 1Registry statusCompletedStudy of Danicopan in Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH)
NCT03053102 · start 2017-03-31
Registered record
- Registry ID
- NCT03053102
- Conditions
- Paroxysmal Nocturnal Hemoglobinuria (PNH)
- Interventions
- Danicopan
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2017-03-31
- Completion
- 2018-11-14
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionParoxysmal Nocturnal Hemoglobinuria (PNH)InterventionDanicopanPhasePhase 2Registry statusCompletedStudy of Different Forms of Danicopan (Tablet, Softgel Capsule, Liquid-filled Capsule) in Healthy Participants
NCT04940559 · start 2016-08-02
Registered record
- Registry ID
- NCT04940559
- Conditions
- Healthy
- Interventions
- Danicopan - Tablet; Danicopan - Softgel; Danicopan - LFC
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2016-08-02
- Completion
- 2016-10-05
- Enrolment
- 26
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionDanicopan - Tablet; Danicopan - Softgel; Danicopan - LFCPhasePhase 1Registry statusCompletedStudy of Multiple Doses of Danicopan in Healthy Participants
NCT04889690 · start 2016-05-21
Registered record
- Registry ID
- NCT04889690
- Conditions
- Healthy
- Interventions
- Danicopan; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2016-05-21
- Completion
- 2017-01-11
- Enrolment
- 45
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionDanicopan; PlaceboPhasePhase 1Registry statusCompletedStudy of a Single Dose of Danicopan in Healthy Participants
NCT04889677 · start 2016-02-04
Registered record
- Registry ID
- NCT04889677
- Conditions
- Healthy
- Interventions
- Danicopan; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2016-02-04
- Completion
- 2016-06-21
- Enrolment
- 44
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionDanicopan; PlaceboPhasePhase 1Registry statusCompletedDanicopan Early Access Program
NCT05982938
Registered record
- Registry ID
- NCT05982938
- Conditions
- Paroxysmal Nocturnal Hemoglobinuria; PNH; Extravascular Hemolysis
- Interventions
- Danicopan
- Study type
- EXPANDED_ACCESS
- Phase
- Not recorded
- Registry status
- Available
- Start
- Not recorded
- Completion
- Not recorded
- Enrolment
- Not recorded
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionParoxysmal Nocturnal Hemoglobinuria; PNH; Extravascular HemolysisInterventionDanicopanPhaseNot recordedRegistry statusAvailable