The World’s First-in-Class Intrauterine Drug-Eluting System
SHANGHAI, Aug. 23, 2024 /PRNewswire/ — Corina Intrauterine Drug-Eluting System (“Corina”), developed by Yipurun (Shanghai) Biotechnology Co., Ltd. (“YPR”), has received approval in China (G.X.Z.Z. 20243181461) for use in patients with moderate-to-severe intrauterine adhesions (IUA) who undergo transcervical resection of adhesions (TCRA). The approval for this indication is based on a randomized controlled clinical trial that demonstrated Corina’s superior efficacy compared to the standard-of-care. Corina is a first-in-class treatment focused on promoting female reproductive health through the prevention of intrauterine re-adhesion risk post TCRA, and the improvement of endometrial growth.
Intrauterine adhesions (IUA) are the formation of scar tissues in the endometrial cavity as a result of damages to the endometrial basal layer of the uterus, which leads to the partial or complete occlusion of the cervical canal and uterine cavity. Clinically, IUA can cause a range of symptoms such as reduced menstrual flow, amenorrhea, infertility and recurrent miscarriage – thereby posing a serious threat to the reproductive health of women of childbearing age. Currently, the incidence rate of IUA in China remains high, and continues to grow due to an increased number of intrauterine interventions. Research in this field show the incidence rate of IUA in China to be as high as 25% in women who have had prior abortion or curettage procedures [1] — this has become a key driver of reduced menstrual flow and secondary infertility in women of childbearing age. As a standard surgical procedure to treat IUA, TCRA separates the adherent tissues and restores the anatomical shape of the uterine cavity. Surveys show 1.6 to 1.8 million patients in China undergo TCRA every year, but the recurrence rate of IUA after surgery is still as high as 62.5% [2]; and the pregnancy success rate of patients after TCRA surgery is only 22.5%~33.3% [3-4]. Over the years, a variety of adjuvant therapies, such as uterine cavity isolation barriers and hormonal treatments, have emerged with limited efficacy.
Corina is an innovative drug-device-combination therapy made from non-degradable, medical grade material, carrying the active ingredient estradiol. Designed to conform to the shape of the female uterus, Corina acts as a physical barrier upon insertion, and enables targeted delivery of estradiol to the endometrium. With YPR’s proprietary controlled-release technology, Corina can continuously release the active substance up to 60 days post procedure to promote endometrium growth.
The registration study results of Corina have demonstrated statistically significant and clinically meaningful reduction in intrauterine adhesion at 60 days post procedure, compared to standard-of-care therapy. Corina has also shown meaningful improvement in endometrial thickness from baseline at 60 days post procedure, compared to standard-of-care therapy.
About Puyi Biotech
Located in the Zhangjiang Hi-Tech Park in Shanghai, Yipurun (Shanghai) Biotechnology Co., Ltd. (‘YPR’) is a wholly-owned subsidiary of Puyi (Shanghai) Biotechnology Co., Ltd. (“Puyi Biotech” or “Group”). Leveraging its knowhow in biomedical material science and its proprietary drug-eluting technology, Puyi Biotech and YPR have developed an innovative R&D pipeline of high-end implantable therapeutics. Since its founding in 2012, Puyi Biotech has focused on providing innovative solutions to address unmet clinical needs across women’s health, ENT (ear, nose and throat), and medical aesthetics categories. The Group has a number of renowned institutions as investors including Goldman Sachs Alternatives, Legend Capital and Northern Light VC.
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References |
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[1] 2015 Chinese expert consensus on the clinical diagnosis and treatment of intrauterine adhesions |
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[2] Yu D , Wong YM , Cheong Y ,et al. Asherman syndrome: one century later[J]. Fertil Steril, 2008,89(4):759–779. |
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[3] Yu D , Li TC , Xia E ,et al. Factors affecting reproductive outcome of hysteroscopic adhesiolysis for Asherman’s syndrome[J]. Fertil Steril, 2008,89(3):715–722. |
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[4] Roy KK , Baruah J , Sharma JB ,et al. Reproductive outcome following hysteroscopic adhesiolysis in patients with infertility due to Asherman’s syndrome[J]. Arch Gynecol Obstet, 2010,281(2):355–361. |
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