U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C21H25ClO6.C3H8O2.H2O
Molecular Weight 502.982
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DAPAGLIFLOZIN PROPANEDIOL

SMILES

O.C[C@H](O)CO.CCOC1=CC=C(CC2=C(Cl)C=CC(=C2)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C1

InChI

InChIKey=GOADIQFWSVMMRJ-UPGAGZFNSA-N
InChI=1S/C21H25ClO6.C3H8O2.H2O/c1-2-27-15-6-3-12(4-7-15)9-14-10-13(5-8-16(14)22)21-20(26)19(25)18(24)17(11-23)28-21;1-3(5)2-4;/h3-8,10,17-21,23-26H,2,9,11H2,1H3;3-5H,2H2,1H3;1H2/t17-,18-,19+,20-,21+;3-;/m10./s1

HIDE SMILES / InChI

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C3H8O2
Molecular Weight 76.0944
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula C21H25ClO6
Molecular Weight 408.873
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Dapagliflozin (trade name Farxiga in the U.S. and Forxiga in the EU and Russia) is a drug of the gliflozin class, developed by Bristol-Myers Squibb in partnership with AstraZeneca. Farxiga is a sodium-glucose cotransporter 2 (SGLT2) inhibitor indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Originator

Curator's Comment: # Bristol-Myers Squibb

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
FARXIGA

Approved Use

FARXIGA (dapagliflozin) is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus

Launch Date

2014
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
154 ng/mL
10 mg single, oral
dose: 10 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN 3-O-GLUCURONIDE plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
24.6 ng/mL
2.5 mg single, oral
dose: 2.5 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN 3-O-GLUCURONIDE plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
49 ng/mL
5 mg single, oral
dose: 5 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN 3-O-GLUCURONIDE plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
118 ng/mL
10 mg single, oral
dose: 10 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
24.8 ng/mL
2.5 mg single, oral
dose: 2.5 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
48.4 ng/mL
5 mg single, oral
dose: 5 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
119 ng/mL
10 mg 1 times / day steady-state, oral
dose: 10 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: HEALTHY
age: UNKNOWN
sex: UNKNOWN
food status: FASTED
116 ng/mL
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: HEALTHY
age: UNKNOWN
sex: UNKNOWN
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
208 ng*h/mL
5 mg single, oral
dose: 5 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN 3-O-GLUCURONIDE plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
612 ng*h/mL
10 mg single, oral
dose: 10 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN 3-O-GLUCURONIDE plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
95.8 ng*h/mL
2.5 mg single, oral
dose: 2.5 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN 3-O-GLUCURONIDE plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
105 ng*h/mL
2.5 mg single, oral
dose: 2.5 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN 3-O-GLUCURONIDE plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
232 ng*h/mL
5 mg single, oral
dose: 5 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN 3-O-GLUCURONIDE plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
658 ng*h/mL
10 mg single, oral
dose: 10 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN 3-O-GLUCURONIDE plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
189 ng*h/mL
5 mg single, oral
dose: 5 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
418 ng*h/mL
10 mg single, oral
dose: 10 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
92.3 ng*h/mL
2.5 mg single, oral
dose: 2.5 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
101 ng*h/mL
2.5 mg single, oral
dose: 2.5 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
199 ng*h/mL
5 mg single, oral
dose: 5 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
427 ng*h/mL
10 mg single, oral
dose: 10 mg
route of administration: oral
experiment type: single
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: unhealthy
age: Children
sex:
food status:
506 ng × h/mL
10 mg 1 times / day steady-state, oral
dose: 10 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: HEALTHY
age: UNKNOWN
sex: UNKNOWN
food status: FASTED
368 ng × h/mL
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: HEALTHY
age: UNKNOWN
sex: UNKNOWN
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
15.77 h
10 mg 1 times / day steady-state, oral
dose: 10 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: HEALTHY
age: UNKNOWN
sex: UNKNOWN
food status: FASTED
3 h
10 mg single, oral
dose: 10 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DAPAGLIFLOZIN plasma
Homo sapiens
population: HEALTHY
age: UNKNOWN
sex: UNKNOWN
food status: FASTED
Doses

Doses

DosePopulationAdverse events​
10 mg single, oral
Highest studied dose
Dose: 10 mg
Route: oral
Route: single
Dose: 10 mg
Sources:
unhealthy, 14.6 years (range: 11–17)
n = 8
Health Status: unhealthy
Condition: type 2 diabetes mellitus
Age Group: 14.6 years (range: 11–17)
Sex: M+F
Population Size: 8
Sources:
Other AEs: Abdominal pain upper, Back pain...
Other AEs:
Abdominal pain upper (12.5%)
Back pain (12.5%)
Nausea (12.5%)
Sources:
10 mg 1 times / day steady, oral
Recommended
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy, 23 years
n = 1
Health Status: unhealthy
Condition: type 2 diabetes mellitus
Age Group: 23 years
Sex: F
Population Size: 1
Sources:
Disc. AE: Ketoacidosis...
AEs leading to
discontinuation/dose reduction:
Ketoacidosis (1 patient)
Sources:
50 mg single, oral
Highest studied dose
Dose: 50 mg
Route: oral
Route: single
Dose: 50 mg
Sources:
healthy, 24 years (range: 20–45 years years)
n = 8
Health Status: healthy
Age Group: 24 years (range: 20–45 years years)
Sex: M
Population Size: 8
Sources:
20 mg 1 times / day steady, oral
Highest studied dose
Dose: 20 mg, 1 times / day
Route: oral
Route: steady
Dose: 20 mg, 1 times / day
Sources:
unhealthy, 62 years (range: 20 - 70 years)
n = 12
Health Status: unhealthy
Condition: type 2 diabetes mellitus
Age Group: 62 years (range: 20 - 70 years)
Sex: M
Population Size: 12
Sources:
Other AEs: Protein urine present...
Other AEs:
Protein urine present (2 patients)
Sources:
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 139
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 139
Sources:
Other AEs: Coronary artery disease, Gastritis...
Other AEs:
Coronary artery disease (serious, 1 patient)
Gastritis (serious, 1 patient)
Lung infection (serious, 1 patient)
Acidosis (serious, 1 patient)
Osteoarthritis (serious, 1 patient)
Colorectal cancer (serious, 1 patient)
Syncope (serious, 1 patient)
Ectopic pregnancy (serious, 1 patient)
Calculus ureteric (serious, 1 patient)
Hydronephrosis (serious, 1 patient)
Hyperlipidaemia (below serious, 31 patient)
Sources:
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 12
Health Status: unhealthy
Condition: Metabolic Syndrome
Population Size: 12
Sources:
Other AEs: Urinary infection...
Other AEs:
Urinary infection (below serious, 1 patient)
Sources:
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 18
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 18
Sources:
Other AEs: Muscle soreness...
Other AEs:
Muscle soreness (below serious, 8 patients)
Sources:
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 22
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 22
Sources:
Other AEs: Increased urinary frequency, Vaginal itching...
Other AEs:
Increased urinary frequency (below serious, 3 patients)
Vaginal itching (below serious, 2 patients)
Nausea (below serious, 1 patient)
Dry mouth (below serious, 2 patients)
Urinary tract infection (below serious, 1 patient)
Sources:
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 12
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 12
Sources:
Other AEs: Urinary tract infection, Low back pain...
Other AEs:
Urinary tract infection (below serious, 2 patients)
Low back pain (below serious, 1 patient)
Sources:
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 15
Health Status: unhealthy
Condition: PreDiabetes
Population Size: 15
Sources:
Other AEs: Vaginal infection, Urinary tract infections...
Other AEs:
Vaginal infection (below serious, 3 patients)
Urinary tract infections (below serious, 2 patients)
Sources:
2.5 mg 1 times / day steady, oral
Dose: 2.5 mg, 1 times / day
Route: oral
Route: steady
Dose: 2.5 mg, 1 times / day
Sources:
unhealthy
n = 74
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 74
Sources:
Other AEs: Uterine leiomyoma, Pneumonia...
Other AEs:
Uterine leiomyoma (serious, 1 patient)
Pneumonia (serious, 1 patient)
Pharyngitis (below serious, 4 patients)
Dizziness (below serious, 5 patients)
Sources:
AEs

AEs

AESignificanceDosePopulation
Abdominal pain upper 12.5%
10 mg single, oral
Highest studied dose
Dose: 10 mg
Route: oral
Route: single
Dose: 10 mg
Sources:
unhealthy, 14.6 years (range: 11–17)
n = 8
Health Status: unhealthy
Condition: type 2 diabetes mellitus
Age Group: 14.6 years (range: 11–17)
Sex: M+F
Population Size: 8
Sources:
Back pain 12.5%
10 mg single, oral
Highest studied dose
Dose: 10 mg
Route: oral
Route: single
Dose: 10 mg
Sources:
unhealthy, 14.6 years (range: 11–17)
n = 8
Health Status: unhealthy
Condition: type 2 diabetes mellitus
Age Group: 14.6 years (range: 11–17)
Sex: M+F
Population Size: 8
Sources:
Nausea 12.5%
10 mg single, oral
Highest studied dose
Dose: 10 mg
Route: oral
Route: single
Dose: 10 mg
Sources:
unhealthy, 14.6 years (range: 11–17)
n = 8
Health Status: unhealthy
Condition: type 2 diabetes mellitus
Age Group: 14.6 years (range: 11–17)
Sex: M+F
Population Size: 8
Sources:
Ketoacidosis 1 patient
Disc. AE
10 mg 1 times / day steady, oral
Recommended
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy, 23 years
n = 1
Health Status: unhealthy
Condition: type 2 diabetes mellitus
Age Group: 23 years
Sex: F
Population Size: 1
Sources:
Protein urine present 2 patients
20 mg 1 times / day steady, oral
Highest studied dose
Dose: 20 mg, 1 times / day
Route: oral
Route: steady
Dose: 20 mg, 1 times / day
Sources:
unhealthy, 62 years (range: 20 - 70 years)
n = 12
Health Status: unhealthy
Condition: type 2 diabetes mellitus
Age Group: 62 years (range: 20 - 70 years)
Sex: M
Population Size: 12
Sources:
Hyperlipidaemia below serious, 31 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 139
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 139
Sources:
Acidosis serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 139
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 139
Sources:
Calculus ureteric serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 139
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 139
Sources:
Colorectal cancer serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 139
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 139
Sources:
Coronary artery disease serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 139
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 139
Sources:
Ectopic pregnancy serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 139
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 139
Sources:
Gastritis serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 139
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 139
Sources:
Hydronephrosis serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 139
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 139
Sources:
Lung infection serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 139
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 139
Sources:
Osteoarthritis serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 139
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 139
Sources:
Syncope serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 139
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 139
Sources:
Urinary infection below serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 12
Health Status: unhealthy
Condition: Metabolic Syndrome
Population Size: 12
Sources:
Muscle soreness below serious, 8 patients
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 18
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 18
Sources:
Nausea below serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 22
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 22
Sources:
Urinary tract infection below serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 22
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 22
Sources:
Dry mouth below serious, 2 patients
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 22
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 22
Sources:
Vaginal itching below serious, 2 patients
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 22
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 22
Sources:
Increased urinary frequency below serious, 3 patients
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 22
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 22
Sources:
Low back pain below serious, 1 patient
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 12
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 12
Sources:
Urinary tract infection below serious, 2 patients
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 12
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 12
Sources:
Urinary tract infections below serious, 2 patients
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 15
Health Status: unhealthy
Condition: PreDiabetes
Population Size: 15
Sources:
Vaginal infection below serious, 3 patients
10 mg 1 times / day steady, oral
Dose: 10 mg, 1 times / day
Route: oral
Route: steady
Dose: 10 mg, 1 times / day
Sources:
unhealthy
n = 15
Health Status: unhealthy
Condition: PreDiabetes
Population Size: 15
Sources:
Pharyngitis below serious, 4 patients
2.5 mg 1 times / day steady, oral
Dose: 2.5 mg, 1 times / day
Route: oral
Route: steady
Dose: 2.5 mg, 1 times / day
Sources:
unhealthy
n = 74
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 74
Sources:
Dizziness below serious, 5 patients
2.5 mg 1 times / day steady, oral
Dose: 2.5 mg, 1 times / day
Route: oral
Route: steady
Dose: 2.5 mg, 1 times / day
Sources:
unhealthy
n = 74
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 74
Sources:
Pneumonia serious, 1 patient
2.5 mg 1 times / day steady, oral
Dose: 2.5 mg, 1 times / day
Route: oral
Route: steady
Dose: 2.5 mg, 1 times / day
Sources:
unhealthy
n = 74
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 74
Sources:
Uterine leiomyoma serious, 1 patient
2.5 mg 1 times / day steady, oral
Dose: 2.5 mg, 1 times / day
Route: oral
Route: steady
Dose: 2.5 mg, 1 times / day
Sources:
unhealthy
n = 74
Health Status: unhealthy
Condition: Type 2 Diabetes
Population Size: 74
Sources:
OverviewDrug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
no [IC50 >45 uM]
no [IC50 >45 uM]
no [IC50 >45 uM]
no [IC50 >45 uM]
no [IC50 >45 uM]
no [IC50 >45 uM]
no (co-administration study)
Comment: no clinically meaningful drug-drug interaction observed in the all the DDI studies conducted
Page: 63, 67
no [IC50 >45 uM]
no (co-administration study)
Comment: no clinically meaningful drug-drug interaction observed in the all the DDI studies conducted
Page: 63, 67
no [IC50 >45 uM]
no (co-administration study)
Comment: no clinically meaningful drug-drug interaction observed in the all the DDI studies conducted
Page: 63, 67
no [IC50 >57.6 uM]
no (co-administration study)
Comment: dapagliflozin does not demonstrate any ability to inhibit P-gp mediated efflux of digoxin
Page: 64, 67
no
no
no
no
no
no
no (co-administration study)
Comment: no clinically meaningful drug-drug interaction observed in the all the DDI studies conducted
Page: 64, 67
weak [IC50 >45 uM]
yes [IC50 33 uM]
no (co-administration study)
Comment: no clinically meaningful drug-drug interaction observed in the all the DDI studies conducted
Page: 64, 67
yes [IC50 69 uM]
yes [IC50 8 uM]
Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
minor
no
no
no
no
no (co-administration study)
Comment: no clinically meaningful drug-drug interaction observed in the all the DDI studies conducted from clinical pharmacology review p67
Page: 29.0
weak
yes
yes
yes
yes
yes
yes
no (co-administration study)
Comment: no clinically meaningful drug-drug interaction observed in the all the DDI studies conducted
Page: 63, 65
yes
no (co-administration study)
Comment: no clinically meaningful drug-drug interaction observed in the all the DDI studies conducted
Page: 63, 65
yes
no (co-administration study)
Comment: no clinically meaningful drug-drug interaction observed in the all the DDI studies conducted
Page: 63, 65
yes
no (co-administration study)
Comment: no clinically meaningful drug-drug interaction observed in the all the DDI studies conducted from clinical pharmacology review p67
Page: 29.0
yes
unlikely (co-administration study)
Comment: coadministration of mefenamic acid showed slight increase in dapagliflozin exposure; the increase in exposure does not warrant any dose adjustment
Page: 65.0
PubMed

PubMed

TitleDatePubMed
Dapagliflozin, a selective SGLT2 inhibitor, improves glucose homeostasis in normal and diabetic rats.
2008 Jun
Dapagliflozin, an oral sodium glucose cotransporter type 2 inhibitor for the treatment of type 2 diabetes mellitus.
2009 Dec
Dapagliflozin for the treatment of type 2 diabetes.
2009 Jul
Renal sodium-glucose transport: role in diabetes mellitus and potential clinical implications.
2009 Jun
Gateways to clinical trials.
2009 Mar
Diabetes treatment.
2009 Mar
Dapagliflozin: an emerging treatment option in type 2 diabetes.
2009 Mar
Dapagliflozin, a novel, selective SGLT2 inhibitor, improved glycemic control over 2 weeks in patients with type 2 diabetes mellitus.
2009 May
Dapagliflozin, a novel SGLT2 inhibitor, induces dose-dependent glucosuria in healthy subjects.
2009 May
Gateways to clinical trials.
2009 Oct
Dapagliflozin: where does it fit in the treatment of type 2 diabetes?
2009 Oct
A study of dapagliflozin in patients with type 2 diabetes receiving high doses of insulin plus insulin sensitizers: applicability of a novel insulin-independent treatment.
2009 Sep
Dapagliflozin: BMS 512148; BMS-512148.
2010
Synthesis of pyridazine and thiazole analogs as SGLT2 inhibitors.
2010 Aug 15
A novel strategy for the treatment of diabetes mellitus - sodium glucose co-transport inhibitors.
2010 Dec
Quantitative PCR tissue expression profiling of the human SGLT2 gene and related family members.
2010 Dec
Dapagliflozin: a sodium glucose cotransporter 2 inhibitor in development for type 2 diabetes.
2010 Dec
Effect of dapagliflozin in patients with type 2 diabetes who have inadequate glycaemic control with metformin: a randomised, double-blind, placebo-controlled trial.
2010 Jun 26
Dapagliflozin, an SGLT2 inhibitor, for diabetes.
2010 Jun 26
Dapagliflozin monotherapy in type 2 diabetic patients with inadequate glycemic control by diet and exercise: a randomized, double-blind, placebo-controlled, phase 3 trial.
2010 Oct
Patents

Sample Use Guides

The recommended starting dose is 5 mg once daily, taken in the morning, with or without food. Dose can be increased to 10 mg once daily in patients tolerating FARXIGA who require additional glycemic control.
Route of Administration: Oral
In Vitro Use Guide
Curator's Comment: A non-radioactive cell-based method for the screening of SGLT inhibitors using COS-7 cells transiently expressing human SGLT1 (hSGLT1), CHO-K1 cells stably expressing human SGLT2 (hSGLT2), and a novel fluorescent d-glucose analogue 1-NBDG as a substrate was used.
The IC50 values of dapagliflozin for hSGLT2 and hSGLT1 determined using 1-NBDG were 1.86 nM and 880 nM
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:28:40 GMT 2023
Edited
by admin
on Fri Dec 15 15:28:40 GMT 2023
Record UNII
887K2391VH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DAPAGLIFLOZIN PROPANEDIOL
USAN  
USAN  
Official Name English
DAPAGLIFLOZIN COMPOUND WITH (2S)-1,2-PROPANEDIOL HYDRATE
MI  
Common Name English
FARXIGA
Brand Name English
XIGDUO COMPONENT DAPAGLIFLOZIN PROPANEDIOL
Brand Name English
DAPAGLIFLOZIN PROPYLENE GLYCOLATE HYDRATE
JAN  
Common Name English
DAPAGLIFLOZIN PROPANEDIOL MONOHYDRATE [EMA EPAR]
Common Name English
DAPAGLIFLOZIN PROPANEDIOL COMPONENT OF XIGDUO
Brand Name English
BMS-512148-05
Code English
(2S,3R,4R,5S,6R)-2-(4-CHLORO-3-(4-ETHOXYBENZYL)PHENYL)-6-(HYDROXYMETHYL)TETRAHYDRO- 2H-PYRAN-3,4,5-TRIOL, (2S)-PROPANE-1,2-DIOL (1:1) MONOHYDRATE
Common Name English
DAPAGLIFLOZIN PROPANEDIOL MONOHYDRATE
EMA EPAR   WHO-DD  
Common Name English
DAPAGLIFLOZIN PROPYLENE GLYCOLATE HYDRATE [JAN]
Common Name English
DAPAGLIFLOZIN S-PROPYLENE GLYCOL MONOHYDRATE
Common Name English
DAPAGLIFLOZIN COMPOUND WITH (2S)-1,2-PROPANEDIOL HYDRATE [MI]
Common Name English
Dapagliflozin propanediol monohydrate [WHO-DD]
Common Name English
DAPAGLIFLOZIN PROPANEDIOL [USAN]
Common Name English
D-GLUCITOL, 1,5-ANHYDRO-1-C-(4-CHLORO-3-((4-ETHOXYPHENYL)METHYL)PHENYL)-, (1S)-, COMPD. WITH (2S)-1,2-PROPANEDIOL, HYDRATE (1:1:1)
Common Name English
FORXIGA
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C98083
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
Code System Code Type Description
CAS
1700615-13-9
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
NON-SPECIFIC STEREOCHEMISTRY
RXCUI
1486966
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY RxNorm
MERCK INDEX
m4086
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY Merck Index
DAILYMED
887K2391VH
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY
ChEMBL
CHEMBL429910
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY
EVMPD
SUB90205
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY
DRUG BANK
DBSALT001101
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY
PUBCHEM
24906252
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID00914678
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY
NCI_THESAURUS
C154296
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY
FDA UNII
887K2391VH
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY
CHEBI
85079
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY
CAS
960404-48-2
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY
RS_ITEM_NUM
1163253
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY
JAPANESE REVIEW
FORXIGA
Created by admin on Fri Dec 15 15:28:40 GMT 2023 , Edited by admin on Fri Dec 15 15:28:40 GMT 2023
PRIMARY APPROVED MARCH 2014
Related Record Type Details
PARENT -> SALT/SOLVATE
ANHYDROUS->SOLVATE
Related Record Type Details
METABOLITE INACTIVE -> PARENT
Related Record Type Details
ACTIVE MOIETY