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

Details

Stereochemistry ABSOLUTE
Molecular Formula C28H31NO2
Molecular Weight 413.5512
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LASOFOXIFENE

SMILES

OC1=CC=C2[C@H]([C@H](CCC2=C1)C3=CC=CC=C3)C4=CC=C(OCCN5CCCC5)C=C4

InChI

InChIKey=GXESHMAMLJKROZ-IAPPQJPRSA-N
InChI=1S/C28H31NO2/c30-24-11-15-27-23(20-24)10-14-26(21-6-2-1-3-7-21)28(27)22-8-12-25(13-9-22)31-19-18-29-16-4-5-17-29/h1-3,6-9,11-13,15,20,26,28,30H,4-5,10,14,16-19H2/t26-,28+/m1/s1

HIDE SMILES / InChI
Lasofoxifene is an active component of Fablyn. Fablyn is used for the treatment of osteoporosis in postmenopausal women. Lasofoxifene is a nonsteroidal selective estrogen receptor modulator. Lasofoxifene has no effect on CYP2E1- or CYP2D6-mediated drug metabolism and should not affect drugs metabolized by other cytochrome P450 isoenzymes. Common adverse reactions considered to be related to Fablyn therapy were muscle spasms, hot flush and vaginal discharge. Lasofoxifene approved in the EU in 2009 is now withdrawn from use in the European Union.

Originator

Curator's Comment: # Ligand Pharmaceuticals; Pfizer

Approval Year

Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
0.218 μg/mL
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
0.09 ng/mL
0.01 mg 1 times / day steady-state, oral
dose: 0.01 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
0.25 ng/mL
0.03 mg 1 times / day steady-state, oral
dose: 0.03 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
0.74 ng/mL
0.1 mg 1 times / day steady-state, oral
dose: 0.1 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
2.08 ng/mL
0.3 mg 1 times / day steady-state, oral
dose: 0.3 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
6.43 ng/mL
1 mg 1 times / day steady-state, oral
dose: 1 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
0.169 ng/mL
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
0.173 ng/mL
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
0.214 ng/mL
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: MALE
food status: FASTED
0.25 ng/mL
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
0.5 ng/mL
0.5 mg single, oral
dose: 0.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
0.1 ng/mL
0.1 mg single, oral
dose: 0.1 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
0.24 ng/mL
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
0.44 ng/mL
0.5 mg single, oral
dose: 0.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
0.09 ng/mL
0.1 mg single, oral
dose: 0.1 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
52.7 ng × h/mL
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
1.67 ng × h/mL
0.01 mg 1 times / day steady-state, oral
dose: 0.01 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
5.14 ng × h/mL
0.03 mg 1 times / day steady-state, oral
dose: 0.03 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
15.7 ng × h/mL
0.1 mg 1 times / day steady-state, oral
dose: 0.1 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
43.2 ng × h/mL
0.3 mg 1 times / day steady-state, oral
dose: 0.3 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
137 ng × h/mL
1 mg 1 times / day steady-state, oral
dose: 1 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
38.1 ng × h/mL
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
37.1 ng × h/mL
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
52.6 ng × h/mL
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: MALE
food status: FASTED
45.8 ng × h/mL
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
85.5 ng × h/mL
0.5 mg single, oral
dose: 0.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
14.5 ng × h/mL
0.1 mg single, oral
dose: 0.1 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
45.6 ng × h/mL
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
77.5 ng × h/mL
0.5 mg single, oral
dose: 0.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
14.5 ng × h/mL
0.1 mg single, oral
dose: 0.1 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
196 h
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
182 h
0.03 mg 1 times / day steady-state, oral
dose: 0.03 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
171 h
0.1 mg 1 times / day steady-state, oral
dose: 0.1 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
147 h
0.3 mg 1 times / day steady-state, oral
dose: 0.3 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
134 h
1 mg 1 times / day steady-state, oral
dose: 1 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: FASTED
193 h
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
195 h
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
252 h
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: MALE
food status: FASTED
151.1 h
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
134.8 h
0.5 mg single, oral
dose: 0.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
164.3 h
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
146.3 h
0.5 mg single, oral
dose: 0.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
0.508%
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
0.717%
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
0.433%
0.25 mg single, oral
dose: 0.25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
LASOFOXIFENE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: MALE
food status: FASTED
Doses

Doses

DosePopulationAdverse events​
1 mg 1 times / day steady-state, oral
Highest studied dose
Dose: 1 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 1 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Other AEs: Hot flushes, Leg cramps...
Other AEs:
Hot flushes (18 patients)
Leg cramps (15 patients)
Leukorrhea (7 patients)
Vaginal bleeding (2 patients)
Fractures (5 patients)
Leg cramps (7%)
Leg cramps (2%)
Sources:
0.25 mg single, oral
Studied dose
Dose: 0.25 mg
Route: oral
Route: single
Dose: 0.25 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Other AEs: somnolence, Headache...
Other AEs:
somnolence (2 patients)
Headache (1 pt)
nausea (1 pt)
Sources:
0.25 mg 1 times / day steady-state, oral
Studied dose
Dose: 0.25 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 0.25 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Other AEs: Breast pain, Hot flushes...
Other AEs:
Breast pain (4 patients)
Hot flushes (24 patients)
Leg cramps (20 patients)
Leukorrhea (12 patients)
Vaginal bleeding (3 patients)
Fractures (3 patients)
hot flushes (4%)
Sources:
20 mg single, oral
Studied dose
Dose: 20 mg
Route: oral
Route: single
Dose: 20 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M
Food Status: UNKNOWN
Sources:
AEs

AEs

AESignificanceDosePopulation
Leg cramps 15 patients
1 mg 1 times / day steady-state, oral
Highest studied dose
Dose: 1 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 1 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Hot flushes 18 patients
1 mg 1 times / day steady-state, oral
Highest studied dose
Dose: 1 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 1 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Vaginal bleeding 2 patients
1 mg 1 times / day steady-state, oral
Highest studied dose
Dose: 1 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 1 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Leg cramps 2%
1 mg 1 times / day steady-state, oral
Highest studied dose
Dose: 1 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 1 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Fractures 5 patients
1 mg 1 times / day steady-state, oral
Highest studied dose
Dose: 1 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 1 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Leukorrhea 7 patients
1 mg 1 times / day steady-state, oral
Highest studied dose
Dose: 1 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 1 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Leg cramps 7%
1 mg 1 times / day steady-state, oral
Highest studied dose
Dose: 1 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 1 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Headache 1 pt
0.25 mg single, oral
Studied dose
Dose: 0.25 mg
Route: oral
Route: single
Dose: 0.25 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
nausea 1 pt
0.25 mg single, oral
Studied dose
Dose: 0.25 mg
Route: oral
Route: single
Dose: 0.25 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
somnolence 2 patients
0.25 mg single, oral
Studied dose
Dose: 0.25 mg
Route: oral
Route: single
Dose: 0.25 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Leukorrhea 12 patients
0.25 mg 1 times / day steady-state, oral
Studied dose
Dose: 0.25 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 0.25 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Leg cramps 20 patients
0.25 mg 1 times / day steady-state, oral
Studied dose
Dose: 0.25 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 0.25 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Hot flushes 24 patients
0.25 mg 1 times / day steady-state, oral
Studied dose
Dose: 0.25 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 0.25 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Fractures 3 patients
0.25 mg 1 times / day steady-state, oral
Studied dose
Dose: 0.25 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 0.25 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Vaginal bleeding 3 patients
0.25 mg 1 times / day steady-state, oral
Studied dose
Dose: 0.25 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 0.25 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
Breast pain 4 patients
0.25 mg 1 times / day steady-state, oral
Studied dose
Dose: 0.25 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 0.25 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
hot flushes 4%
0.25 mg 1 times / day steady-state, oral
Studied dose
Dose: 0.25 mg, 1 times / day
Route: oral
Route: steady-state
Dose: 0.25 mg, 1 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: F
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
Selective estrogen receptor modulator (SERM) lasofoxifene forms reactive quinones similar to estradiol.
2012-07-16
Lasofoxifene in osteoporosis and its place in therapy.
2010-12
Third-generation SERMs may face uphill battle.
2010-11-17
Tipping the balance for the primary prevention of breast cancer.
2010-11-17
Breast cancer incidence in the randomized PEARL trial of lasofoxifene in postmenopausal osteoporotic women.
2010-11-17
What is the best balance of benefits and risks among anti-resorptive therapies for postmenopausal osteoporosis?
2010-11
Lasofoxifene and cardiovascular events in postmenopausal women with osteoporosis: Five-year results from the Postmenopausal Evaluation and Risk Reduction with Lasofoxifene (PEARL) trial.
2010-10-26
Evidence-based guidelines for the pharmacological treatment of postmenopausal osteoporosis: a consensus document by the Belgian Bone Club.
2010-10
New selective estrogen receptor modulators (SERMs) in development.
2010-09
Long-term safety and efficacy of raloxifene in the prevention and treatment of postmenopausal osteoporosis: an update.
2010-08-09
Therapeutics. Lasofoxifene reduced vertebral fractures in postmenopausal women with osteoporosis.
2010-07-20
Interest of lasofoxifene in the treatment of osteoporosis. Evaluation of "Lasofoxifene in postmenopausal women with osteoporosis". N Engl J Med 2010;362:686-96.
2010-07
Safety of bazedoxifene in a randomized, double-blind, placebo- and active-controlled Phase 3 study of postmenopausal women with osteoporosis.
2010-06-22
Lasofoxifene: Evidence of its therapeutic value in osteoporosis.
2010-06-15
Lasofoxifene for postmenopausal women with osteoporosis.
2010-06-10
Lasofoxifene for postmenopausal women with osteoporosis.
2010-06-10
Lasofoxifene for postmenopausal women with osteoporosis.
2010-06-10
An innovative method to classify SERMs based on the dynamics of estrogen receptor transcriptional activity in living animals.
2010-04
SERMs in the prevention and treatment of postmenopausal osteoporosis: an update.
2010-03
Another selective estrogen-receptor modulator for osteoporosis.
2010-02-25
Lasofoxifene in postmenopausal women with osteoporosis.
2010-02-25
Selective estrogen receptor modulator (SERM) for the treatment of osteoporosis in postmenopausal women: focus on lasofoxifene.
2010-02-02
Endometrial safety: a key hurdle for selective estrogen receptor modulators in development.
2010-01-29
Gene expression profiling studies of three SERMs and their conjugated estrogen combinations in human breast cancer cells: insights into the unique antagonistic effects of bazedoxifene on conjugated estrogens.
2010-01
Modulators of androgen and estrogen receptor activity.
2010
Recent advances in managing osteoporosis.
2009-12-15
Lasofoxifene: new drug. Osteoporosis: no better than raloxifene.
2009-12
A randomised, double-blinded, placebo-controlled, trial to determine the individual response in bone turnover markers to lasofoxifene therapy.
2009-12
Current and emerging pharmacologic therapies for the management of postmenopausal osteoporosis.
2009-10
Lasofoxifene, a new selective estrogen receptor modulator for the treatment of osteoporosis and vaginal atrophy.
2009-09
Thresholds for therapies: highlights of the St Gallen International Expert Consensus on the primary therapy of early breast cancer 2009.
2009-08
New selective estrogen and androgen receptor modulators.
2009-07
Treatment of osteoporosis with annual iv zoledronic acid: effects on hip fracture.
2009-04
Effects of various selective estrogen receptor modulators with or without conjugated estrogens on mouse mammary gland.
2009-04
Designing the ideal selective estrogen receptor modulator--an achievable goal?
2009-02-03
Lasofoxifene for the prevention and treatment of postmenopausal osteoporosis.
2009
Progress in osteoporosis and fracture prevention: focus on postmenopausal women.
2009
Clinical issues regarding cardiovascular disease and selective estrogen receptor modulators in postmenopausal women.
2009
Docking study of triphenylphosphonium cations as estrogen receptor alpha modulators.
2009
Bazedoxifene for the prevention of postmenopausal osteoporosis.
2008-12
Effects of selective oestrogen receptor modulators on proliferation in tissue cultures of pre- and postmenopausal human endometrium.
2008-11
Metabolism, distribution, and excretion of a next generation selective estrogen receptor modulator, lasofoxifene, in rats and monkeys.
2008-09
Effects of lasofoxifene on the uterus, vagina, and breast in ovariectomized cynomolgus monkeys (Macaca fascicularis).
2008-08
Disposition of lasofoxifene, a next-generation selective estrogen receptor modulator, in healthy male subjects.
2008-07
Hormone-dependent aging problems in women.
2008-06-30
Activity of three selective estrogen receptor modulators on hormone-dependent responses in the mouse uterus and mammary gland.
2008-06-11
Selective estrogen receptor modulators: an update on recent clinical findings.
2008-03
Bazedoxifene: bazedoxifene acetate, TSE 424, TSE-424, WAY 140424.
2008
[Status of novel bone-targeting SERMs in development].
2007-11-28
Management of age-related osteoporosis and prevention of associated fractures.
2006-09
Patents

Sample Use Guides

500 ug daily. The tablet may be taken any time of day without regard to food and beverage intake.
Route of Administration: Oral
In Vitro Use Guide
Lasofoxifene was determined to be an extremely potent antagonist to the growth of estrogen-dependent MCF-7 breast cancer cell line (IC50 =0.05 nM).
Name Type Language
LASOFOXIFENE
EMA EPAR   INN   MART.   MI   WHO-DD  
INN  
Official Name English
LASOFOXIFENE [EMA EPAR]
Preferred Name English
Lasofoxifene [WHO-DD]
Common Name English
LASOFOXIFENE [MI]
Common Name English
LASOFOXIFENE [MART.]
Common Name English
(-)-CIS-5,6,7,8-TETRAHYDRO-6-PHENYL-5-(P-(2-(1-PYRROLIDINYL)ETHOXY)PHENYL)-2-NAPHTHOL
Common Name English
lasofoxifene [INN]
Common Name English
Classification Tree Code System Code
WHO-VATC QG03XC03
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NCI_THESAURUS C1821
Created by admin on Mon Mar 31 18:17:56 GMT 2025 , Edited by admin on Mon Mar 31 18:17:56 GMT 2025
WHO-ATC G03XC03
Created by admin on Mon Mar 31 18:17:56 GMT 2025 , Edited by admin on Mon Mar 31 18:17:56 GMT 2025
Code System Code Type Description
CHEBI
135938
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PRIMARY
SMS_ID
100000092767
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PRIMARY
PUBCHEM
216416
Created by admin on Mon Mar 31 18:17:56 GMT 2025 , Edited by admin on Mon Mar 31 18:17:56 GMT 2025
PRIMARY
DRUG CENTRAL
4308
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PRIMARY
EPA CompTox
DTXSID50171037
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PRIMARY
DRUG BANK
DB06202
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PRIMARY
CAS
180916-16-9
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PRIMARY
NCI_THESAURUS
C80679
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PRIMARY
FDA UNII
337G83N988
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PRIMARY
MERCK INDEX
m6700
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PRIMARY Merck Index
WIKIPEDIA
Lasofoxifene
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PRIMARY
EVMPD
SUB27754
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PRIMARY
INN
7875
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PRIMARY
ChEMBL
CHEMBL328190
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PRIMARY