Exercise and Nutritional Rehabilitation in Patients With Cancer, Randomised (1:1) Unblinded Feasibility Trial of a Rehabilitation Programme (Exercise and Nutrition) Versus Waiting List Control, in Patients With Advanced Cancer
In patients with incurable cancer, general deterioration in their ability to walk, exercise and care for themselves is often regarded as an inevitable consequence of this. In 2015, Hospice UK published a report advocating "Rehabilitative Palliative Care".
However there is limited robust evidence on which to base this approach. Reviews of the literature show limited study numbers but do suggest that rehabilitation may be feasible for advanced cancer patients. However key components were not clear and no recommendations could be given.
This trial is designed primarily to test the feasibility of a rehabilitation programme (exercise and nutritional supplementation) in advanced cancer patients. Feasibility will be the primary outcome measure including rates of recruitment and compliance. Secondary outcome measures include impact on physical function, nutritional status, quality of life for patients and their carers. We will also assess the health economic impact by assessing patient health facility use throughout the trial.
40 patients with advanced cancer living in the community will be recruited from two hospice palliative care teams in Edinburgh. These patients will be randomised in to either the treatment arm: the rehabilitation programme plus standard care, or the control arm: standard care alone. The treatment arm will consist of an 8 week rehabilitation programme, supervised at weekly clinics by a physiotherapist and dietician.
To minimise contamination the control group will be offered the treatment at the end of the 8 weeks (waiting list control).
Measurements will be made for both groups and compared at baseline (week 0), midpoint (week 5) and endpoint (week 9). Recommendations for a larger UK wide trial will be made from the findings of this study.
100 项与 Accord Clinical Research 相关的临床结果
0 项与 Accord Clinical Research 相关的专利(医药)
复宏汉霖宣布,该公司合作伙伴Accord公司(Intas美国子公司)于近日收到美国FDA通知,由复宏汉霖自主研发、生产的曲妥珠单抗生物类似药(HLX02,中国商品名为汉曲优)获美国批准上市,用于辅助治疗人表皮生长因子受体-2(HER2)过表达的乳腺癌、HER2过表达的转移性乳腺癌,以及HER2过表达的转移性胃腺癌或胃食管交界腺癌。至此,该单抗生物类似药产品已在中国、欧盟、美国获批。
根据复宏汉霖新闻稿介绍,曲妥珠单抗是治疗HER2阳性乳腺癌和胃癌的基石类药物。自2020年7月及8月先后于欧盟和中国获批上市以来,汉曲优目前已于英国、法国、德国、瑞士、澳大利亚、芬兰、西班牙、阿根廷、沙特阿拉伯、泰国等超过40个国家和地区获批上市。
此次获FDA批准主要基于复宏汉霖递交的全面的分析结果、临床前及临床研究数据。自2015年以来,复宏汉霖针对汉曲优开展了一系列的头对头比对研究,包括质量对比研究、临床1期和国际多中心临床3期研究等。这些数据充分证明了汉曲优与原研曲妥珠单抗在质量、安全性和有效性方面高度相似。
参考资料:[1]汉霖头条 | 复宏汉霖曲妥珠单抗获美国FDA批准上市. Retrieved Apr 26, 2024, from https://mp.weixin.qq.com/s/jm_fpFCLVsH4VAzZ1EoLUw
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100 项与 Accord Clinical Research 相关的药物交易
100 项与 Accord Clinical Research 相关的转化医学