Details
Stereochemistry | ACHIRAL |
Molecular Formula | C31H34F2N6O2 |
Molecular Weight | 560.6375 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1CCN(CC1)C2=CC(NC3CCOCC3)=C(C=C2)C(=O)NC4=NNC5=CC=C(CC6=CC(F)=CC(F)=C6)C=C45
InChI
InChIKey=HAYYBYPASCDWEQ-UHFFFAOYSA-N
InChI=1S/C31H34F2N6O2/c1-38-8-10-39(11-9-38)25-3-4-26(29(19-25)34-24-6-12-41-13-7-24)31(40)35-30-27-17-20(2-5-28(27)36-37-30)14-21-15-22(32)18-23(33)16-21/h2-5,15-19,24,34H,6-14H2,1H3,(H2,35,36,37,40)
Molecular Formula | C31H34F2N6O2 |
Molecular Weight | 560.6375 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionCurator's Comment: Description was created based on several sources, including
http://ignyta.com/providers/rx-precision-medicine-pipeline/entrectinib/
http://www.medscape.com/viewarticle/862131
Curator's Comment: Description was created based on several sources, including
http://ignyta.com/providers/rx-precision-medicine-pipeline/entrectinib/
http://www.medscape.com/viewarticle/862131
Entrectinib (previously known as RXDX-101, NMS-E628) is an investigational drug, potent inhibitor of ALK, ROS1, and, importantly, of TRK family kinases, which shows promise for therapy of tumors bearing oncogenic forms of these proteins. Entrectinib (RXDX-101) is a selective inhibitor for all three Trk receptor tyrosine kinases encoded by the three NTRK genes, as well as the ROS1 and ALKreceptor tyrosine kinases.This investigational drug is active at low nanomolar concentrations, allowing for once-daily oral administration to patients whose tumors have been shown to have gene rearrangements in NTRK, ROS1, or ALK. Nerviano Medical Sciences, the original sponsor for entrectinib (formerly referred to as
NMS-1191372), initiated the first-in-human Phase 1 study ALKA-372-001 in Italy in October 2012. The study is currently ongoing in Italy. Entrectinib is currently being tested in a global phase 2 basket clinical trial called STARTRK-2. In the U.S., entrectinib has orphan drug designation and rare pediatric disease designation for the treatment of neuroblastoma and orphan drug designation for treatment of TrkA-, TrkB-, TrkC-, ROS1- and ALK-positive non-small cell lung cancer (NSCLC) and metastatic colorectal cancer (mCRC).
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27003761
Curator's Comment: efficiently penetrant the blood-brain barrier (BBB) in different animal species and highly efficacious in in vivo xenograft models.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
1.7 nM [IC50] | |||
0.1 nM [IC50] | |||
0.1 nM [IC50] | |||
0.2 nM [IC50] | |||
1.6 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
2250 nM |
600 mg single, oral dose: 600 mg route of administration: Oral experiment type: SINGLE co-administered: |
ENTRECTINIB plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
31800 nM × h |
600 mg single, oral dose: 600 mg route of administration: Oral experiment type: SINGLE co-administered: |
ENTRECTINIB plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
20 h |
600 mg single, oral dose: 600 mg route of administration: Oral experiment type: SINGLE co-administered: |
ENTRECTINIB plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
Funbound
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
1% |
600 mg single, oral dose: 600 mg route of administration: Oral experiment type: SINGLE co-administered: |
ENTRECTINIB plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
Doses
Dose | Population | Adverse events |
---|---|---|
550 mg/m2 1 times / day steady, oral Dose: 550 mg/m2, 1 times / day Route: oral Route: steady Dose: 550 mg/m2, 1 times / day Sources: |
unhealthy, 2-21 years n = 6 Health Status: unhealthy Age Group: 2-21 years Population Size: 6 Sources: |
DLT: Creatinine increased... Dose limiting toxicities: Creatinine increased (grade 2, 1 patient) Sources: |
750 mg/m2 1 times / day steady, oral Dose: 750 mg/m2, 1 times / day Route: oral Route: steady Dose: 750 mg/m2, 1 times / day Sources: |
unhealthy, 2-21 years n = 3 Health Status: unhealthy Age Group: 2-21 years Population Size: 3 Sources: |
DLT: Dysgeusia, Fatigue... Dose limiting toxicities: Dysgeusia (grade 2, 1 patient) Sources: Fatigue (grade 2, 1 patient) Pulmonary edema (grade 3, 1 patient) |
800 mg 1 times / day steady, oral Dose: 800 mg, 1 times / day Route: oral Route: steady Dose: 800 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 18–80 years) n = 65 Health Status: unhealthy Age Group: 55 years (range: 18–80 years) Sex: M+F Population Size: 65 Sources: |
DLT: Cognitive disturbance, Fatigue... Other AEs: Eosinophilic myocarditis... Dose limiting toxicities: Cognitive disturbance (grade 3, 1 patient) Other AEs:Fatigue (grade 3, 1 patient) Eosinophilic myocarditis (grade 4, 1 patient) Sources: |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Disc. AE: Pneumonia, Cardio-respiratory arrest... AEs leading to discontinuation/dose reduction: Pneumonia (0.3%) Sources: Cardio-respiratory arrest (0.6%) Dyspnea (0.6%) Fatigue (0.6%) |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Disc. AE: Blood creatinine increased, Fatigue... AEs leading to discontinuation/dose reduction: Blood creatinine increased (4%) Sources: Fatigue (3.7%) Anemia (3.1%) Diarrhea (2.8%) Pyrexia (2.8%) Dizziness (2.5%) Dyspnea (2.3%) Nausea (2.3%) Pneumonia (2.3%) Cognitive disorder (2%) Neutropenia (2%) Weight increased (1.4%) |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 149 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 149 |
Disc. AE: Pulmonary edema, Pulmonary embolism... AEs leading to discontinuation/dose reduction: Pulmonary edema (0.3%) Sources: Page: p. 149Pulmonary embolism (0.3%) Myocarditis (0.3%) Cardiogenic shock (0.3%) Pericardial effusion (0.3%) Malaise (0.3%) Peripheral edema (0.3%) Sepsis (0.3%) |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 150 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 150 |
Disc. AE: Decreased appetite, Hypotension... AEs leading to discontinuation/dose reduction: Decreased appetite (1.1%) Sources: Page: p. 150Hypotension (1.1%) Hypoxia (0.8%) |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 151 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 151 |
Disc. AE: Arthralgia... AEs leading to discontinuation/dose reduction: Arthralgia (1%) Sources: Page: p. 151 |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Creatinine increased | grade 2, 1 patient DLT |
550 mg/m2 1 times / day steady, oral Dose: 550 mg/m2, 1 times / day Route: oral Route: steady Dose: 550 mg/m2, 1 times / day Sources: |
unhealthy, 2-21 years n = 6 Health Status: unhealthy Age Group: 2-21 years Population Size: 6 Sources: |
Dysgeusia | grade 2, 1 patient DLT |
750 mg/m2 1 times / day steady, oral Dose: 750 mg/m2, 1 times / day Route: oral Route: steady Dose: 750 mg/m2, 1 times / day Sources: |
unhealthy, 2-21 years n = 3 Health Status: unhealthy Age Group: 2-21 years Population Size: 3 Sources: |
Fatigue | grade 2, 1 patient DLT |
750 mg/m2 1 times / day steady, oral Dose: 750 mg/m2, 1 times / day Route: oral Route: steady Dose: 750 mg/m2, 1 times / day Sources: |
unhealthy, 2-21 years n = 3 Health Status: unhealthy Age Group: 2-21 years Population Size: 3 Sources: |
Pulmonary edema | grade 3, 1 patient DLT |
750 mg/m2 1 times / day steady, oral Dose: 750 mg/m2, 1 times / day Route: oral Route: steady Dose: 750 mg/m2, 1 times / day Sources: |
unhealthy, 2-21 years n = 3 Health Status: unhealthy Age Group: 2-21 years Population Size: 3 Sources: |
Cognitive disturbance | grade 3, 1 patient DLT, Disc. AE |
800 mg 1 times / day steady, oral Dose: 800 mg, 1 times / day Route: oral Route: steady Dose: 800 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 18–80 years) n = 65 Health Status: unhealthy Age Group: 55 years (range: 18–80 years) Sex: M+F Population Size: 65 Sources: |
Fatigue | grade 3, 1 patient DLT, Disc. AE |
800 mg 1 times / day steady, oral Dose: 800 mg, 1 times / day Route: oral Route: steady Dose: 800 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 18–80 years) n = 65 Health Status: unhealthy Age Group: 55 years (range: 18–80 years) Sex: M+F Population Size: 65 Sources: |
Eosinophilic myocarditis | grade 4, 1 patient | 800 mg 1 times / day steady, oral Dose: 800 mg, 1 times / day Route: oral Route: steady Dose: 800 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 18–80 years) n = 65 Health Status: unhealthy Age Group: 55 years (range: 18–80 years) Sex: M+F Population Size: 65 Sources: |
Pneumonia | 0.3% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Cardio-respiratory arrest | 0.6% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Dyspnea | 0.6% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Fatigue | 0.6% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Weight increased | 1.4% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Cognitive disorder | 2% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Neutropenia | 2% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Dyspnea | 2.3% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Nausea | 2.3% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Pneumonia | 2.3% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Dizziness | 2.5% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Diarrhea | 2.8% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Pyrexia | 2.8% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Anemia | 3.1% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Fatigue | 3.7% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Blood creatinine increased | 4% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: |
Cardiogenic shock | 0.3% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 149 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 149 |
Malaise | 0.3% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 149 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 149 |
Myocarditis | 0.3% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 149 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 149 |
Pericardial effusion | 0.3% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 149 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 149 |
Peripheral edema | 0.3% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 149 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 149 |
Pulmonary edema | 0.3% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 149 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 149 |
Pulmonary embolism | 0.3% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 149 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 149 |
Sepsis | 0.3% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 149 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 149 |
Hypoxia | 0.8% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 150 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 150 |
Decreased appetite | 1.1% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 150 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 150 |
Hypotension | 1.1% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 150 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 150 |
Arthralgia | 1% Disc. AE |
600 mg 1 times / day steady, oral Recommended|MTD Dose: 600 mg, 1 times / day Route: oral Route: steady Dose: 600 mg, 1 times / day Sources: Page: p. 151 |
unhealthy, 55 years (range: 4 - 86 years) n = 355 Health Status: unhealthy Age Group: 55 years (range: 4 - 86 years) Sex: M+F Population Size: 355 Sources: Page: p. 151 |
Overview
CYP3A4 | CYP2C9 | CYP2D6 | hERG |
---|---|---|---|
OverviewOther
Other Inhibitor | Other Substrate | Other Inducer |
---|---|---|
Drug as perpetrator
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: NDA212726-115 |
likely | no (co-administration study) Comment: Clinical DDI study with midazolam showed no induction. Page: NDA212726-115 |
||
Page: NDA212726-115, 134 |
weak | yes (co-administration study) Comment: Coadministration of entrectinib single dose 600 mg (one hour prior to digoxin (0.5 mg) administration) increased the Cmax and AUC of P‐gp substrate digoxin by 28% and 18%, respectively. Dose adjustment for P‐gp substrate when coadministered with P‐gp inhibitor is not needed. Page: NDA212726-115, 134 |
||
Page: NDA212726-115 |
yes | |||
Page: NDA212726-115 |
yes | |||
Page: NDA212726-115 |
yes | |||
Page: NDA212726-115 |
yes | |||
Page: NDA212726-115 |
yes | |||
yes | ||||
yes | ||||
Page: NDA212726-115 |
yes | |||
Page: NDA212726-115 |
yes | |||
Page: NDA212726-115 |
yes | |||
Page: NDA212726-115 |
yes | |||
Page: NDA212726-115 |
yes | |||
Page: NDA212726-115, 132, 133 |
yes | yes (co-administration study) Comment: Coadministration of entrectinib did not increase the AUC of midazolam (sensitive CYP3A4 substrate, 2 mg SD) after a single dose 600 mg but increase the AUC of midazolam (2 mg SD) by 50% after repeat dosing at 600 mg (14 days). Cmax of midazolam were decreased by 34% after a single dose and 21% after repeat dosing (14 days) of entrectinib. No dose adjustment is needed for sensitive CYP3A substrates when coadministered with entrectinib. Page: NDA212726-115, 132, 133 |
Drug as victim
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: NDA212725-90; NDA-212726-110, 111, 130, 131 |
major | yes (co-administration study) Comment: When a single dose of 100 mg entrectinib is coadministered with strong CYP3A inhibitor itraconazole, the GMR (90% CI) of Cmax, AUClast and AUCINF of entrectinib were 1.73 (1.37, 2.18), 5.26 (4.01, 6.91) and 6.04 (4.54, 8.04), respectively. Dose adjustment is recommended when entrectinib is coadministered with strong or moderate CYP3A4 inhibitors. Coadministration of entrectinib (600 mg SD) with multiple doses of a strong CYP3A4 inducer rifampin (600 mg QD x 14 days) decreased the Cmax and AUCINF of entrectinib by 56% and 77%, respectively. Coadministration of strong or moderate inducers of CYP3A4 with entrectinib should be avoided. Page: NDA212725-90; NDA-212726-110, 111, 130, 131 |
||
Page: NDA212726-110 |
minor | |||
Page: NDA212726-114 |
no | |||
Page: NDA212726-114 |
no | |||
Page: NDA212726-114 |
no | |||
Page: NDA212726-114 |
no | |||
Page: NDA212726-114 |
yes | |||
Page: NDA212726-114 |
yes | |||
Page: NDA212726-114, 130, 131, 132 |
yes | yes (co-administration study) Comment: When a single dose of 100 mg entrectinib is coadministered with strong CYP3A inhibitor itraconazole, AUClast and AUCINF of M5 were increased by 86% and 152%, respectively, while there was a 38% decrease of Cmax for M5. Coadministration of entrectinib (600 mg SD) with multiple doses of a strong CYP3A4 inducer rifampin (600 mg QD x 14 days) decreased the Cmax and AUCINF of M5 by 75% and 87%, respectively. Page: NDA212726-114, 130, 131, 132 |
Tox targets
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: NDA212725-44, 56; NDA212726-59, 71 |
PubMed
Title | Date | PubMed |
---|---|---|
ALK inhibitors in non-small cell lung cancer: crizotinib and beyond. | 2014 Jul |
|
Entrectinib: a potent new TRK, ROS1, and ALK inhibitor. | 2015 |
|
Activity of second-generation ALK inhibitors against crizotinib-resistant mutants in an NPM-ALK model compared to EML4-ALK. | 2015 Jul |
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT02587650
600 mg orally daily per cycle (28 days). To be taken within 1 hour following a meal.
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:22:26 GMT 2023
by
admin
on
Sat Dec 16 09:22:26 GMT 2023
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Record UNII |
L5ORF0AN1I
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Record Status |
Validated (UNII)
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Record Version |
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Common Name | English | ||
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Code | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C129825
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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FDA ORPHAN DRUG |
587117
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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FDA ORPHAN DRUG |
462414
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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FDA ORPHAN DRUG |
462914
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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NCI_THESAURUS |
C1967
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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FDA ORPHAN DRUG |
463014
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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Code System | Code | Type | Description | ||
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DTXSID101026450
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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L5ORF0AN1I
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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5345
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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DB11986
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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10132
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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L5ORF0AN1I
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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100000163524
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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2197862
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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CD-95
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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Entrectinib
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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25141092
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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SUB177830
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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CHEMBL1983268
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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C114984
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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1108743-60-7
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY | |||
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m12164
Created by
admin on Sat Dec 16 09:22:27 GMT 2023 , Edited by admin on Sat Dec 16 09:22:27 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
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EXCRETED UNCHANGED |
AMOUNT EXCRETED
FECAL
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TARGET -> INHIBITOR |
COMPETITIVE INHIBITOR
IC50
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METABOLIC ENZYME -> SUBSTRATE |
MINOR
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TARGET -> INHIBITOR |
INHIBITOR
IC50
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METABOLIC ENZYME -> SUBSTRATE |
Metabolism of entrectinib is primary mediated by CYP3A4 (> 90%)
MAJOR
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TARGET -> INHIBITOR |
INHIBITOR
IC50
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TARGET -> INHIBITOR |
INHIBITOR
IC50
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BINDER->LIGAND |
BINDING
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Related Record | Type | Details | ||
---|---|---|---|---|
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METABOLITE ACTIVE -> PARENT |
MAJOR
PLASMA
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Related Record | Type | Details | ||
---|---|---|---|---|
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ACTIVE MOIETY |
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Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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blood‐to‐plasma ratio | PHARMACOKINETIC |
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Tmax | PHARMACOKINETIC |
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ORAL ADMINISTRATION |
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Biological Half-life | PHARMACOKINETIC |
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