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英文药名：Conbriza（Bazedoxifene Acetate filmcoated tablets） 中文药名：醋酸巴多昔芬片 生产厂家：辉瑞制药
*In the osteoporosis treatment trial in 7,492 evaluable subjects (mean age=66 years), the bazedoxifene-treated women had an increased risk of venous thromboembolism (deep vein thrombosis, pulmonary embolism and retinal vein thrombosis). The rate per 1,000 women-years through the 3-year study period was 2.86 in the bazedoxifene 20 mg group and 1.76 in the placebo group, and through the 5-year study period was 2.34 in the bazedoxifene 20 mg group and 1.56 in the placebo group. The rate per 1,000 women-years through the 7 year study period was 2.06 in the bazedoxifene 20 mg group and 1.36 in the placebo group. The rate of VTE was highest in the first year with a relative risk of 2.69. After 3 years the relative risk was 1.63 and after a 5 year study period the relative risk was 1.50. After 7 year study period the relative risk was 1.51 (see section 5.1). Other venous thromboembolic events could also occur. Post-marketing experience There have been post-marketing reports of ocular events other than retinal vein thrombosis. These reports include visual acuity reduced, blurred vision, photopsia, visual field defect, visual impairment, dry eye, eyelid oedema, blepharospasm, eye pain and eye swelling. The underlying nature of these events is uncertain. If ocular symptoms occur, patients should be advised to seek medical attention. Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via HPRA Pharmacovigilance, Earlsfort Terrace, IRL - Dublin 2, Tel: +353 1 6764971, Fax: +353 1 6762517, Website: www.hpra.ie E-mail: medsafety@hpra.ie 4.9 Overdose In the case of overdose, there is no specific antidote, and treatment should be symptomatic. 5. PHARMACOLOGICAL PROPERTIES 5.1 Pharmacodynamic properties Pharmacotherapeutic group: Selective estrogen receptor modulator, ATC code: G03XC02. Mechanism of action Bazedoxifene belongs to a class of compounds known as selective estrogen receptor modulators (SERMs). Bazedoxifene acts as both an oestrogen-receptor agonist and/or antagonist, depending upon the cell and tissue type and target genes. Bazedoxifene decreases bone resorption and reduces biochemical markers of bone turnover to the premenopausal range. These effects on bone remodeling lead to an increase in bone mineral density (BMD), which in turn contributes to a reduction in the risk of fractures. Bazedoxifene functions primarily as an oestrogen-receptor antagonist in uterine and breast tissues. Clinical efficacy The efficacy of bazedoxifene was established in two multicentre, double-blind, randomised, placebo- and active-control, Phase 3 trials: 3-year osteoporosis treatment trial and a 2-year osteoporosis prevention trial. Osteoporosis treatment trial In the osteoporosis treatment study, 7,492 postmenopausal women (mean age of 66 years; range 50 to 85 years and a mean time of 19.5 years since menopause) received bazedoxifene (20 or 40 mg daily), raloxifene (60 mg daily), or placebo to evaluate the incidence of new vertebral fractures over 3 years (3-year core study). The 3-year core study was extended twice, with two 2-year double-blind, placebo-controlled extensions, resulting in a total treatment duration of up to 7 years (7-year study). A total of 3,146 subjects continued into the first 2-year extension (bazedoxifene 20 mg: n=1,047, bazedoxifene 40/20 mg: n=1,041, placebo: n=1,058). The bazedoxifene 40 mg dose was decreased to a 20 mg dose after approximately 4 years. The raloxifene group was discontinued during the first 2-year extension. A total of 1,732 subjects continued into the second 2-year extension (bazedoxifene 20 mg: n=560, bazedoxifene 40/20 mg: n=582, and placebo: n=590). All subjects were to receive 1,200 mg of elemental calcium and 400 IU of vitamin D daily. This study included mostly Caucasian (87.3%) subjects who were either osteoporotic without baseline vertebral fracture (BMD T-score at lumbar spine [LS] or femoral neck [FN] between -2.5 and -4.0) or osteoporotic, with at least 1 mild baseline vertebral fracture. The mean LS and FN T-scores at baseline were -2.4 and -1.7, respectively. There was a significant reduction in the incidence of new vertebral fractures after 3 years of treatment with bazedoxifene 20 mg (42%), bazedoxifene 40mg (37%) and raloxifene 60 mg (42%) compared to placebo. The reduction in the incidence of vertebral fracture was similar among bazedoxifene and raloxifene treatment groups. The treatment effect was similar among those with and without prevalent vertebral fractures (Table 1).
b p-value=0.015 c p-value=0.22 d p-value=0.035 After 5 years of treatment, the incidence of new vertebral fractures remained lower in the bazedoxifene 20 mg group (4.49%) compared to placebo (6.82%) with a relative risk reduction of 36% (p=0.014). After 7 years of treatment, the incidence of new vertebral fractures remained lower in the bazedoxifene 20 mg group (7.64%) compared to placebo (9.90%) with a relative risk reduction of 30% (p=0.022). The incidence of non-vertebral osteoporosis-related fractures was similar among bazedoxifene 20 mg (5.68%), raloxifene 60 mg (5.87%), and placebo (6.26%) groups. In a post-hoc analysis, the 10-year fracture probability as an index of baseline fracture risk was determined. The mean 10-year fracture probability of a major osteoporotic fracture for the entire study population was 11%. In subjects treated with bazedoxifene, the incidence of fractures was related to the baseline fracture risk: the higher the fracture risk, the greater the benefit with bazedoxifene treatment. In subjects with 10-year fracture probabilities at or above 16%, bazedoxifene was associated with a significant decrease in the risk of all clinical fractures. In a post-hoc analysis, the relative risk of non-vertebral fractures in bazedoxifene-treated subjects decreased with increased fracture probability. In subjects with a fracture probability of 20% or greater (n = 618), the risk of non-vertebral fractures in bazedoxifene-treated subjects was decreased by 55% (95% CI: 18-76) compared to placebo-treated subjects. The increase in LS BMD compared with placebo with bazedoxifene 20 mg and raloxifene 60 mg was significant at 6 months (1.02% and 1.29%, respectively) and was maintained through 3 years (1.32% and 2.08%, respectively). The effect of bazedoxifene on BMD at other skeletal sites was similar. The increases in BMD relative to placebo remained statistically significant at all skeletal sites throughout the 5 years of treatment with bazedoxifene. After 7 years of treatment with bazedoxifene the increases in BMD relative to placebo remained statistically significant at the femoral neck, femoral trochanter, and total hip. The increase from baseline in lumbar spine BMD at 7 years in the bazedoxifene 20 mg group was not statistically greater than in the placebo group. Discontinuation from the study was required when excessive bone loss or incident vertebral fractures occurred. Such discontinuation was statistically significant more frequently in the placebo group (4.0%) than in the bazedoxifene 20 mg (2.8%) or raloxifene 60 mg (2.1%) groups. Osteoporosis prevention trial The prevention study (1,583 subjects; mean age, 58 years; mean years since menopause, 11) compared BMD effects of bazedoxifene (10, 20, or 40 mg daily), raloxifene (60 mg daily), and placebo. All subjects received calcium supplementation daily; most received 600 mg calcium (e.g., Caltrate™) daily, while some received up to 1,200 mg daily. This study included subjects who had a LS or FN neck BMD T-score no less than -2.5. The median T-score ranged from -0.6 to -1.4, depending on the skeletal site. BMD was preserved in bazedoxifene 20 mg and raloxifene 60 mg-treated subjects, while significant loss in BMD was observed in patients receiving placebo. The increase in LS BMD with bazedoxifene 20 mg and raloxifene 60 mg, compared with placebo, was significant at 6 months (1.14% and 1.26%, respectively) and was maintained through 2 years (1.41% and 1.49%, respectively). The effect of bazedoxifene on BMD at other skeletal sites was similar. Clinical safety Assessment of bone histomorphometry and bone turnover In the osteoporosis treatment study in 7,492 postmenopausal women (mean age = 66 years), 121 bone biopsies were obtained from iliac crest after the administration of fluorochrome label from the subjects in bazedoxifene, raloxifene and placebo groups (bazedoxifene 20 mg = 28; bazedoxifene 40 mg = 29, raloxifene 60 mg = 32, placebo = 32) after approximately 2 or 3 years of treatment. Histological assessment of bone biopsies from all treatment groups revealed formation of normal lamellar bone in all treated subjects. There was no evidence of osteomalacia, peritrabecular or marrow fibrosis, cellular toxicity or woven bone in any of the bone-biopsy specimens in any of the treatment groups. Histomorphometric assessment revealed normal mineralisation, as evidenced by the presence of normal osteoid thickness, normal mineralisation lag time, and mineral apposition rate. In the osteoporosis treatment study, bazedoxifene 20 mg and raloxifene 60 mg therapy resulted in a significant reduction of serum markers of bone resorption (C-telopeptide) and bone formation (osteocalcin), when compared to placebo, indicating a reduction in bone turnover. Median reductions from baseline over 25% for C-telopeptide and osteocalcin were observed with bazedoxifene therapy. Similar reductions in the rate of bone turnover have been observed in the osteoporosis prevention study. Effects on lipid metabolism and cardiovascular system In the osteoporosis treatment study after 3 years of treatment, bazedoxifene 20 mg and raloxifene 60 mg exhibited significant reductions in serum total cholesterol, low-density lipoprotein (LDL) cholesterol and a significant increase in high-density lipoprotein (HDL) cholesterol compared to placebo. The median percent change from baseline of total cholesterol, LDL cholesterol and HDL cholesterol with bazedoxifene 20 mg were –3.75%, –5.36% and 5.10%, respectively, and were similar to that observed with raloxifene 60 mg. The effect on triglycerides in the bazedoxifene 20 mg and raloxifene 60 mg groups was similar to placebo. This lipid profile was maintained throughout the 7 years of treatment. The treatment effect on lipids was similar in the osteoporosis prevention study. The clinical relevance of these changes has not been established. In the osteoporosis treatment trial in 7,492 subjects (mean age = 66 years), the bazedoxifene-treated women had an increased risk of VTE (deep vein thrombosis, pulmonary embolism and retinal vein thrombosis) (see section 4.8). The highest rate of VTE per 1,000 women-years of follow up was observed during the first year: 4.64 in the bazedoxifene 20 mg group and 1.73 in the placebo group (relative risk 2.69).The rate per 1,000 women-years at 3 years was 2.86 in the bazedoxifene 20 mg group and 1.76 in the placebo group (relative risk 1.63). The rate per 1,000 women-years at 5 years was 2.34 in the bazedoxifene 20 mg group and 1.56 in the placebo group (relative risk 1.50). After 7 years the rate per 1,000 women-years was 2.06 in the bazedoxifene 20 mg group and 1.36 in the placebo group (relative risk 1.51). Cerebrovascular effects In the 3 year core study the rate per 1,000 women-years for ischaemic strokes was similar between the 20 mg bazedoxifene (1.98) and placebo (2.2) groups and higher in the 40 mg bazedoxifene (2.72) group. The rate per 1,000 women years for transient ischaemic attacks (TIA) was similar between the 20 mg bazedoxifene (1.1) and placebo (0.88) groups and higher in the 40 mg bazedoxifene (1.59) group. After 5 years of treatment the rate per 1,000 women-years for ischaemic strokes was similar between the 20 mg bazedoxifene (1.87) and the placebo (2.02) groups. The rate per 1,000 women years for TIA was higher for the 20 mg bazedoxifene group (0.94) compared to placebo (0.62). After 7 years of treatment, the rate per 1,000 women-years for ischaemic strokes was the same for the 20 mg bazedoxifene (1.78) and the placebo (1.78) groups. The rate per 1,000 women years for TIA was higher for the bazedoxifene 20 mg group (0.96) compared to placebo (0.55). Effects on the uterus In the osteoporosis treatment study, transvaginal ultrasonography (TVU) showed minimal changes in endometrial thickness in placebo (-0.08 mm, n=131), bazedoxifene 20 mg (-0.07 mm, n=129), and raloxifene 60 mg (0.16 mm, n=110) treated groups after 2 years. At 3 years, there were no cases of endometrial cancer and 1 case (0.1%) of endometrial hyperplasia in the bazedoxifene 20 mg-treated subjects. There was 1 case (0.1%) of endometrial cancer, 1 case of sarcoma (0.1%), and 1 case (0.1%) of endometrial hyperplasia in the raloxifene 60 mg-treated subjects. There were 3 cases (0.2%) of endometrial cancer and 1 case (0.1%) of endometrial hyperplasia in the placebo group. Endometrial polyps were diagnosed in 10 subjects in the bazedoxifene 20 mg, 17 subjects in the raloxifene 60 mg, and 11 subjects in the placebo treatment groups through month 36. After 5 years of treatment, the endometrial thickness in the bazedoxifene 20 mg group did not change and remained similar to placebo; there were no cases of endometrial cancer in the bazedoxifene 20 mg group compared to 6 cases in the placebo group (p<0.05). After 7 years of treatment, the endometrial thickness in the bazedoxifene 20 mg group did not change and remained similar to placebo; there were no cases of endometrial cancer in the bazedoxifene 20 mg group compared to 7 cases in the placebo group (p<0.008). In the osteoporosis prevention study, TVU showed minimal changes from baseline in endometrial thickness in placebo (-0.24 mm, n=154), bazedoxifene 20 mg (-0.06 mm, n=158) and raloxifene 60 mg (0.01 mm, n=154) treated groups after 2 years. No cases of hyperplasia or endometrial malignancy were identified in any bazedoxifene- or raloxifene-treated subjects. Effects on the breast In the osteoporosis treatment study, the incidence of breast-related adverse events in the bazedoxifene group was similar to placebo at 3 years. There were 5 cases of breast cancer per 4,591 person-years of follow-up in the bazedoxifene 20 mg group (1.09 per 1,000), 7 cases of breast cancer per 4,526 person-years of follow-up in the raloxifene 60 mg group (1.55 per 1,000), and 8 cases of breast cancer per 4,604 person-years of follow-up in the placebo group (1.74 per 1,000). After 5 years of treatment, there were 9 cases of breast cancer in the bazedoxifene 20 mg group (1.40 per 1,000 women-years) and 10 cases in the placebo group (1.56 per 1,000 women-years). After 7 years of treatment, there were 13 cases of breast cancer in the bazedoxifene 20 mg group (1.78 per 1,000 women-years) and 11 cases in the placebo group (1.50 per 1,000 women-years). In the osteoporosis prevention study, the incidence of breast-related adverse events (breast tenderness, pain, breast cancer, benign breast neoplasm) in the bazedoxifene 20 mg and raloxifene 60 mg groups was similar to placebo. In the breast-density study, an ancillary study of the osteoporosis treatment study, 444 postmenopausal women (mean age = 59 years) with osteoporosis from all 4 treatment groups, were evaluated for mammographic breast density changes at 24 months. Mean changes in mammographic breast density in the bazedoxifene 20 mg group were significantly reduced from baseline (-1.45 percentage points, p<0.05) while no changes were observed in the placebo group (-0.15 percentage points). Effects on thyroid and ovarian malignancies In the osteoporosis treatment study in 7,492 postmenopausal women (mean age, 66 years), among 1,886 subjects treated with bazedoxifene (20 mg), there were 5 cases of thyroid cancer (0.69 per 1,000) and among 1,885 subjects treated with placebo, there was 1 case of thyroid cancer (0.14 per 1,000) after 7 years of treatment. There were no cases on thyroid cancer in the 40 mg treatment group up to 5 years. In the osteoporosis treatment study in 7,492 postmenopausal women (mean age, 66 years), among 1,886 subjects treated with bazedoxifene (20 mg), there were 5 cases of ovarian cancer (0.69 per 1,000) and among 1,885 subjects treated with placebo, there were 0 cases of ovarian cancer after 7 years of treatment. There was one case of ovarian cancer in the 40 mg treatment group up to 5 years. 5.2 Pharmacokinetic properties The mean pharmacokinetic parameters of bazedoxifene after multiple doses in healthy postmenopausal ambulatory women who were naturally postmenopausal or who had undergone bilateral oophorectomy are summarized in Table 2.
Bazedoxifene is rapidly absorbed with a tmax of approximately 2 hours and exhibits a linear increase in plasma concentrations for single doses from 0.5 mg up to 120 mg and multiple daily doses from 1 mg to 80 mg. The absolute bioavailability of bazedoxifene is approximately 6%. When single doses of 20 mg bazedoxifene were administered with a high-fat meal, Cmax and AUC increased by 28% and 22%, respectively. An additional study evaluating the effects of a standardized medium-fat meal on the pharmacokinetics of bazedoxifene at steady-state showed a 42% and 35% increase in Cmax and AUC, respectively, when 20 mg bazedoxifene was administered with food. Because these changes are not considered clinically relevant, bazedoxifene can be administered without regard to meals. Distribution Following intravenous administration of a 3 mg dose of bazedoxifene, the volume of distribution is 14.7 ± 3.9 l/kg. Bazedoxifene is highly bound (98% - 99%) to plasma proteins in vitro. Biotransformation The metabolic disposition of bazedoxifene in postmenopausal women has been determined following oral administration of 20 mg of radio-labelled bazedoxifene. Bazedoxifene is extensively metabolised in women. Glucuronidation is the major metabolic pathway. Little or no cytochrome P450-mediated metabolism is evident. Bazedoxifene-5-glucuronide is the major circulating metabolite. The concentrations of this glucuronide are approximately 10-fold higher than those of unchanged active substance in plasma. Elimination Bazedoxifene is eliminated with a half-life of approximately 30 hours. Steady-state concentrations are achieved by the second week of once-daily administration. The apparent oral clearance of bazedoxifene is approximately 4 to 5 l/h/kg. The major route of excretion of radio-labelled bazedoxifene is the faeces, and less than 1% of the dose is eliminated in urine. Special populations Hepatic impairment The disposition of a single 20 mg dose of bazedoxifene was compared in patients with hepatic impairment [Child-Pugh Class A (n=6), B (n=6), and C (n=6)] and subjects with normal hepatic function (n=18). On average, patients with hepatic impairment showed a 4.3-fold increase in AUC compared with controls. Safety and efficacy have not been evaluated further in patients with hepatic insufficiency. Use in this patient population is not recommended (see sections 4.2 and 4.4). Renal impairment Limited clinical data (n=5) are available in subjects with moderate renal impairment (CrCl < 50 ml/min). A single 20 mg dose of bazedoxifene was administered to these subjects. Negligible amounts of bazedoxifene were eliminated in urine. Impaired renal function showed little or no influence on bazedoxifene pharmacokinetics, and no dosing adjustment is required. Elderly patients The pharmacokinetics of a 20 mg single-dose of bazedoxifene were evaluated in a study in 26 healthy postmenopausal women. On average, compared to women 51 to 64 years of age (n=8), women 65 to 74 years of age (n=8) showed a 1.5-fold increase in AUC, and women >75 years of age (n=8) showed a 2.3-fold increase in AUC. This increase was most likely attributed to age-related changes in hepatic function. No dose adjustment is necessary based on age. Paediatric population The pharmacokinetics of bazedoxifene have not been studied in the paediatric population. Race No pharmacokinetic differences based on ethnic group were observed. 5.3 Preclinical safety data In rabbit studies, abortion and an increased incidence of heart (ventricular septal defect) and skeletal system (ossification delays, misshapen or misaligned bones, primarily of the spine and skull) anomalies in the foetuses were present at maternally toxic doses of ≥0.5 mg/kg/day (1.5 times the human exposure). Treatment of rats at maternally toxic doses ≥1 mg/kg/day (≥0.3 times the human exposure) resulted in reduced numbers of live foetuses and/or reductions in foetal body weights. No foetal developmental anomalies were observed. Female rats were administered daily doses of 0.3 to 30 mg/kg (0.03 to 8 times the human exposure) prior to and during mating with untreated males. Oestrous cycles and fertility were adversely affected in all bazedoxifene-treated female groups. The effects of bazedoxifene treatment on bone, uterus, and mammary gland were assessed in ovariectomized rats (0.15 to 1.5 mg/kg/day) and non-human primates [Cynomolgus macaques] (0.2 to 25.0 mg/kg/day). In rats, treatment with bazedoxifene for approximately one year partially prevented the effects of ovariectomy on numerous skeletal parameters (bone mineral content, bone mineral density, and architecture). Additionally, uterine wet weights were reduced compared with untreated animals and histologic evaluation demonstrated little to no difference from the untreated controls. In monkeys, treatment with bazedoxifene for 18 months resulted in the partial preservation of cortical and cancellous bone mass as determined by BMD measurements. The partial preservation of bone mass was achieved by reductions in the ovariectomy-induced increases in bone turnover, evaluated by biochemical markers of bone turnover and histomorphometric indices measured in cancellous and cortical bone. Importantly, in both species, the administration of bazedoxifene had no deleterious effects on bone quality. Like the rodent results, bazedoxifene treatment in non-human primates resulted in uterine and mammary gland atrophy without other histological differentiation from untreated animals. Repeated-dose studies in normally cycling rodents and cynomolgus monkeys revealed a marked stimulation of ovarian follicle growth without ovulation, leading to partly haemorrhagic-ovarian cysts and markedly elevated estradiol levels. This pharmacological effect of bazedoxifene can also be expected in pre-menopausal women, but is considered clinically irrelevant in post-menopausal women. In 6-month carcinogenicity studies in transgenic mice, there was an increased incidence of benign, ovarian granulosa-cell tumours in female mice given 150 or 500 mg/kg/day. Systemic exposure (AUC) to bazedoxifene in these groups was 35 and 69 times that in postmenopausal women administered 20 mg/day for 14 days. In a 2-year carcinogenicity study in rats, an increased incidence of benign, ovarian granulosa-cell tumours was observed in female rats at dietary concentrations of 0.03 and 0.1%. Systemic exposure (AUC) of bazedoxifene in these groups was 2.6 and 6.6 times that observed in postmenopausal women administered 20 mg/day for 14 days. The observation of benign, ovarian granulosa-cell tumours in female mice and rats administered bazedoxifene is a class effect of SERMs, related to its pharmacology in rodents when treated during their reproductive lives, when their ovaries are functional and responsive to hormonal stimulation. Bazedoxifene was not genotoxic or mutagenic in a battery of tests, including in vitro bacterial reverse mutation assay, in vitro mammalian cell forward mutation assay at the thymidine kinase (TK±) locus in L5178Y mouse lymphoma cells, in vitro chromosome aberration assay in Chinese hamster ovary (CHO) cells, and in vivo mouse micronucleus assay. Bazedoxifene caused corticomedullar nephrocalcinosis and enhanced spontaneous chronic progressive nephropathy (CPN) in male rats. Urine parameters were pathologically changed. In long-term studies renal tumours (adenomas and carcinomas) were observed at all doses tested, most likely as a consequence of this chronic renal damage. In the 2-year carcinogenicity study, bazedoxifene, administered orally in the diet to rats at dosages of 0, 0.003%, 0.01%, 0.03%, or 0.1%, resulted in exposures, based on surface area (mg/m2) of approximately 0.6 to 23 times and 0.9 to 31 times in males and females, respectively, the clinical dose of 20 mg. Since chronic progressive nephropathy and corticomedullar nephrocalcinosis are most likely rat-specific nephropathies, these findings are presumably not relevant for humans. In an 18-month bone efficacy study in aged ovariectomized cynomolgus monkeys, bazedoxifene, administered orally to monkeys at dosages of 0, 0.2, 0.5, 1, 5, or 25 mg/kg/day, resulted in exposures, based on surface area (mg/m2) of approximately 0.2 to 24 times the clinical dose of 20 mg. Renal cell carcinomas were observed in this study. These tumours are considered as spontaneous renal cell carcinomas that are known to occur in nonhuman primates and are unlikely to be relevant to humans. 6. PHARMACEUTICAL PARTICULARS 6.1 List of excipient(s) Tablet core: Lactose monohydrate Microcrystalline cellulose Pregelatinised starch (maize) Sodium starch glycolate Sodium lauryl sulfate Colloidal anhydrous silica Magnesium stearate Ascorbic acid Film coating: Hypromellose Titanium dioxide (E171) Macrogol 400 6.2 Incompatibilities Not applicable. 6.3 Shelf life 18 months. 6.4 Special precautions for storage Do not store above 25°C. 6.5 Nature and contents of container PVC/Aclar blister packs of 7, 28, 30, 84, and 90 film-coated tablets. Not all pack sizes may be marketed. 6.6 Special precautions for disposal and other handling No special requirements. 7. MARKETING AUTHORISATION HOLDER Pfizer Limited Ramsgate Road Sandwich Kent CT13 9NJ United Kingdom 8. MARKETING AUTHORISATION NUMBER(S) EU/1/09/511/001 EU/1/09/511/002 EU/1/09/511/003 EU/1/09/511/004 EU/1/09/511/005 9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION Date of first authorisation: 17 April 2009 Date of latest renewal: 17 April 2014 10. DATE OF REVISION OF THE TEXT 05/2015 Detailed information on this medicinal product is available on the website of the European Medicines Agency http://www.ema.europa.eu/. 研究前景： 绝经后骨质疏松症（postmenopausal osteoporosis，POP）是一种与衰老有关的常见病，主要发生在绝经后妇女，由于雌激素缺乏导致骨量减少及骨组织结构变化，使骨脆性增多易于骨折，以及由骨折引起的疼痛、骨骼变形、出现合并症，乃至死亡等问题，严重地影响老年人的身体健康及生活质量，甚至缩短寿命，增加国家及家庭财力与人力负担。与绝经相关的骨质疏松症已是不可忽视的重要保健课题。 妇女绝经后骨质疏松发病率显著高于男性。美国妇女因骨质疏松发生骨折的危险性为17％，而男性为6％。 澳大利亚60岁以上的妇女骨质疏松发病率为58％，男性为28％。我国北京、上海等地流行病学调查显示，60岁以上老年人骨质疏松患病率女性为40％～50％，男性约为20％。巴多昔芬主要适应证为预防和治疗绝经期后骨质疏松症。目前进行的多中心，III期临床研究显示，巴多昔芬联合雌激素可预防骨质丢失，且不会刺激乳腺或子宫。 对于具有正常或低BMD的健康绝经后妇女，SERM（选择性雌激素受体调节剂）能在不刺激子宫内膜的情况下预防骨丢失和降低骨转换。在一项拥有了6847名绝经后骨质疏松症妇女的3年的RCT中（平均年龄66岁），每天20mg或40mg的巴多昔芬能分别使椎骨骨折的发生率降低42%和37%。但对非椎骨骨折无效。巴多昔芬治疗的耐受性与雷洛昔芬相似。与安慰剂组相比能使血管舒缩症状、VET和腿痛性痉挛的发生率增加。 根据骨密度数据，巴多昔芬在骨骼中显示雌激素激动剂活性，能改善脊椎和髋部的骨密度，并显著降低患骨质疏松症的绝经妇女的椎骨骨折风险。这说明巴多昔芬对于子宫内膜有独特的作用。 临床前各模型均未表明巴多昔芬对子宫有雌激素样刺激作用，例如皮下注射巴多昔芬(O．2和2．0mg/kg)并不使未成熟雌性大鼠子宫重量增加或子宫内膜上皮细胞肥大或增生，而雌二醇及RX均有此不良反应。不仅如此，巴多昔芬还能逆转RX对子宫的这种刺激作用。这些结果提示，用巴多昔芬对绝经期后的妇女进行治疗时不会刺激子宫及乳腺细胞。 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
