請輸入關鍵字:

熱門搜尋:

New ESMO Guidelines Include FOTIVDA®▼(tivozanib) Recommendation for Patients with Advanced Renal Cell Carcinoma

日期:2019年3月11日 上午10:06

HEMEL HEMPSTEAD, England -- (BUSINESS WIRE) --

EUSA Pharma (EUSA) welcomes the news that FOTIVDA®▼ (tivozanib) has been included in the new European Society of Medical Oncology (ESMO) clinical practice guidelines for renal cell carcinoma (RCC), published on 21st February 2019.1

In the new guidelines tivozanib is included as a first-line treatment recommendation for advanced RCC (aRCC) clear cell histology patients. The guidelines have also positioned tivozanib as a treatment standard for good (or favourable) risk patients and a treatment option for intermediate risk patients.1

Dr Bernard Escudier, Medical Oncologist and member of the Genitourinary Tumour Board of Gustave Roussy, France, commented “This is excellent news for patients with metastatic RCC. Outcomes in this disease have greatly improved with the introduction of targeted therapies, meaning that patients are living for longer, although currently available therapies can be associated with burdensome toxicities. We are still in need of effective and well tolerated new treatments in metastatic RCC and thus, tivozanib is a welcomed addition. We also look forward to continuing our investigations of potential combination approaches with other therapeutic agents.”

The inclusion of tivozanib in the new guidelines follows the grant of a European Commission (EC) licence in August 2017 for this oral, once-daily,a potent selective vascular endothelial growth factor receptor tyrosine kinase inhibitors (VEGFR-TKI) as first-line treatment of adult patients with aRCC.2

The authorisation within the European Union (EU) was based on evidence from the global, open-label, randomised, multi-centre Phase III trial TiVO-1,which showed that aRCC patients receiving tivozanib experienced improved progression free survival and lower rates of certain adverse events compared to those receiving another VEGFR-TKI, sorafenib.3

“I am pleased that the important European guidelines have been updated to include tivozanib as a recommendation for first line treatment for aRCC,” commented Lee Morley, Chief Executive Officer, EUSA Pharma. “With kidney cancer expected to be one of the fastest increasing cancers over the next ten years,4 we remain committed to ensuring the availability of tivozanib across the EU in line with the indication as a monotherapy in the first-line setting treatment of aRCC.”

Kidney cancer is the 12th most commonly occurring cancer5 worldwide – the 9th in men and the 14th in women, with over 400,000 new cases in 2018.6 RCC is the most common form of kidney cancer, accounting for approximately 80% of cases.1

a 1340 microgram capsule

-ENDS-

NOTES TO EDITORS

About tivozanib

Tivozanib is an oral, once-daily,b potent selective vascular endothelial growth factor receptor tyrosine kinase inhibitors (VEGFR-TKI). It is indicated for the first-line treatment of adult patients with advanced renal cell carcinoma (aRCC) and for adult patients who are VEGFR and mTOR pathway inhibitor-naïve following disease progression after one prior treatment with cytokine therapy for aRCC.2

An over-expression of VEGF protein, and a resulting increase in tumour blood supply (angiogenesis), is a common feature of RCC.3 VEGFR-TKIs reduce the supply of blood to the tumour and are the recommended first-line treatment for advanced RCC in Europe, however, patients often experience significant side effects including fatigue, diarrhoea, and hand-foot syndrome.

In the global Phase III trial (TiVO-1)3 of over 500 patients with advanced RCC, tivozanib demonstrated a significant progression free survival (PFS) benefit versus sorafenib (11.9 vs. 9.1 months in the overall patient population [HR, 0.797; 95% CI, 0.639 to 0.993; P =.042], and 12.7 vs. 9.1 months in treatment-naïve patients [HR, 0.756; 95% CI, 0.580 to 0.985; P =.037]).3 There was also an improved side-effect profile versus sorafenib, with significantly fewer patients on tivozanib (14% versus 43%) requiring a dose reduction due to AEs; and less than 5% of patients experiencing severe side effects (grade 3&4), such as diarrhoea, asthenia (physical weakness) and hand-foot syndrome. Hypertension (44%) and dysphonia (21%) were the most commonly reported AEs on tivozanib.3

Under EUSA Pharma’s license agreement with AVEO PHARMACEUTICALS, INC, announced in December 2015, the company holds exclusive commercialisation rights to tivozanib in RCC in Europe and in a number of other territories outside North America, including South America and South Africa. Under the terms of the agreement, EUSA Pharma will undertake and fund the commercialisation of the product in its territories, assuming licensing. AVEO PHARMACEUTICALS, INC retains the rights to commercialise the product in North America. Tivozanib was discovered by Kyowa Hakko Kirin.

b 1340 microgram capsule

About EUSA Pharma

Founded in March 2015, EUSA Pharma is a world-class biopharmaceutical company focused on oncology and rare disease. The company has commercial operations in the United States and Europe, and a wider distribution network in approximately 40 countries around the world. EUSA Pharma is led by an experienced management team with a strong record of building successful pharmaceutical companies, and is supported by significant funding raised from leading life science investor EW Healthcare Partners. For more information, please visit www.eusapharma.com.

References

1 Escudier B, Porta C, Schmidinger M et al. Renal Cell Carcinoma: ESMO Clinical Practice Guidelines For Diagnosis and Treatment Follow Up. Available at: https://www.esmo.org/Guidelines/Genitourinary-Cancers/Renal-Cell-Carcinoma. Last accessed March 2019.

2 European Medicines Agency. Fotivda. Available at: https://www.ema.europa.eu/medicines/human/EPAR/fotivda. Last accessed March 2019.

3 Motzer R J, Nosov D et al. Tivozanib Versus Sorafenib As Initial Targeted Therapy for Patients With Metastatic Renal Cell Carcinoma: Results From a Phase III Trial. Journal of Clinical Oncology. Volume 31. 2013: 30:3791

4 Cancer Research UK. Kidney cancer rates are increasing, so what’s fuelling the surge? Available at: http://scienceblog.cancerresearchuk.org/2017/04/24/kidney-cancer-rates-are-increasing-so-whats-fuelling-the-surge/. Last accessed March 2019.

5 World Cancer Research Fund, Kidney cancer. Available at: https://www.wcrf.org/dietandcancer/kidney-cancer. Last accessed March 2019.

6 World Cancer Research Fund, Kidney cancer statistics. Available at: https://www.wcrf.org/dietandcancer/cancer-trends/kidney-cancer-statistics. Last accessed March 2019.

View source version on businesswire.com: https://www.businesswire.com/news/home/20190308005271/en/

CONTACT:

Simon Goldsborough
Open Health Patient & Brand Communications
Tel +44 (0)207 861 2808

財華網所刊載內容之知識產權為財華網及相關權利人專屬所有或持有。未經許可,禁止進行轉載、摘編、複製及建立鏡像等任何使用。

如有意願轉載,請發郵件至content@finet.com.hk,獲得書面確認及授權後,方可轉載。

下載財華財經APP,把握投資先機
https://www.finet.com.cn/app

更多精彩内容,請點擊:
財華網(https://www.finet.hk/)
財華智庫網(https://www.finet.com.cn)
現代電視FINTV(https://www.fintv.hk)

相關文章

3月8日
上海宣泰醫藥開發成功的鹽酸普羅帕酮緩釋膠囊由VITRUVIAS THERAPEUTICS INC. 代理於美國上市
3月8日
Impossible Foods在新加坡繼續亞洲擴張之旅
3月8日
CSC提醒企業注意日益增加的DNS劫持
3月8日
SecurDPS Enterprise榮獲SC Media的30週年大獎
3月8日
邁瑞簽署病人安全運動「開放資料承諾」,成為第90家加入改善病人安全的公司
3月8日
第14屆沙迦雙年展啟動,主題為「走出同溫層」
3月8日
AI硬件峰會:在美國大獲成功之後來到北京
3月8日
Carestream Health將其醫療保健IT業務售予飛利浦
3月8日
Impossible Foods在新加坡繼續其亞洲擴張之旅
3月8日
瑞思邁收購HB Healthcare,以幫助韓國數百萬名睡眠呼吸中止症及其他呼吸疾病患者

視頻

快訊

08:42
三花智控(02050.HK)料年度歸屬股東淨利潤同比增長25%-50%
08:13
「國產GPU」集齊了!通用GPU芯片公司「天數智芯」通過港交所聆訊
17:41
滴普科技(01384.HK)與沐曦股份簽訂戰略合作協議
17:34
中廣核電力(01816.HK)調整惠州1號及2號機組預計投入運行時間
17:25
許正宇:香港黃金中央清算系統計劃於2026年試營運
17:13
香港2025年第三季錄得1365億元國際收支赤字
17:02
香港11月份整體消費物價指數同比上升1.2%
16:56
和譽-B(02256.HK)附屬和譽醫藥CSF-1R抑制劑貝捷邁獲國家藥監局批准
16:48
【港股收評】三大指數集體走高!光通訊、黃金股漲勢突出
16:44
悅安新材:公司羰基鐵粉食品添加劑產品目前處於市場導入階段