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中國生物製藥(01177.HK):業績符合預期,腫瘤板塊繼續擴張,維持“買入”評級
格隆匯 11-28 09:37

機構:西南證券

評級:買入

事件:公司2019]年前三季度實現收入193.2億元(+22.8%),其中新產品收入佔比為20.6%;歸母淨利潤22.6億元(+2.5%),調整後歸母淨利潤26億元(+15.7%),總體現金流61.4億元(-2.7%),總體符合預期。

業績符合預期,抗腫瘤板塊持續發力。從收入端看:2019前三季度肝病、抗腫瘤和心腦血管板塊產品依舊佔據主導地位,收入分別為49.7、42和25億元,收入佔比分別為25.7%、21.8%以及12.9%。1)其中肝病品種受帶量採購影響,收入佔比同比降低6.1pp(即增速為-1%),預計將來還會持續萎縮。2)腫瘤板塊增速達到83.4%,收入佔比同比提升7.2pp,一躍成為公司第二大核心板塊;其中安羅替尼收入估計21億元,全年有望衝刺30億,即增速可達到134%;雷替曲塞銷售額達5.4億元(+40%),預計全年超7億元;達沙替尼和硼替佐米收入分別為1.8億元(+47.6%)和1.3億元(211.6%),長勢喜人;從研發管線中豐富的重磅抗腫瘤仿製藥/生物類似藥以及1類新藥儲備來看,該板塊未來將會成為公司最核心的增長動力。從盈利能力看:2019年前三季度公司毛利率、銷售費用率與上年同期基本持平,較為穩定。

研發投入持續創新高,重磅品種已進入收穫期:2019年前三季度公司研發費用為20.5億元(+20.6%),持續創新高。2019年7月至今,公司共收穫8項批件,其中安羅替尼新增軟組織肉瘤以及小細胞肺癌兩個適應症,加上非小細胞肺癌,預計已獲批適應症峯值銷售將達到60億元;此外託法替布以及阿比特龍均為重磅品種,原研藥峯值銷售額分別達到22億美元(預計今年達到峯值)以及35億美元;抗血栓藥替格瑞洛獲得FDA的暫定批准,表明公司的生產和管理能力達到國際先進水平;公司侖伐替尼的上市申請獲CDE受理,或成為首仿品種,原研藥預計2021年專利到期,若2020年公司專利挑戰成功有望超預期上市;PD-1品種預計今年底以cHL適應症2期數據提交上市申請,有望於2020年獲批上市;呼吸系統重磅品種布地奈德預計2020年上市,有望衝刺7億元銷售額;阿達木單抗、凝血因子VIII等大品種均有望於2020年上市。

盈利預測與評級:預計公司19-21年收入及歸母淨利潤複合增速分別為20%、22%,EPS分別為人民幣0.28/0.34/0.42元,對應PE為36X/30X/25X。維持“買入”評級。

風險提示:藥品大幅降價的風險,研發進度不及預期的風險,新產品上市進度或不及預期。

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