INSIDE INDUSTRY

2013 ◽  
Vol 17 (04) ◽  
pp. 63-71

Concert Pharmaceuticals announces completion of enrollment in Phase II CTP-499 clinical trial for the treatment of diabetic kidney disease. NanoLogix bacteria detection plates break longevity records using Anthrax. AngioLight lands strategic partnership with Medical Technologies Innovation Asia. BioScience Managers expands Asia Pacific presence. Simbionix signs an agreement with the Laparoscopic Surgical Skills Foundation. The Institute for Systems Biology and AB SCIEX partner to help make medical care more predictive and personalized. Alchemia appoints Charles Walker as Chief Executive Officer. Anergis expands management team. Novozymes acquires enzyme business from Canadian Iogen Corporation.

2021 ◽  
Vol 10 (6) ◽  
pp. 1254
Author(s):  
Warren W. Pan ◽  
Thomas W. Gardner ◽  
Jennifer L. Harder

Diabetic retinal disease (DRD) remains the most common cause of vision loss in adults of working age. Progress on the development of new therapies for DRD has been limited by the complexity of the human eye, which constrains the utility of traditional research techniques, including animal and tissue culture models—a problem shared by those in the field of kidney disease research. By contrast, significant progress in the study of diabetic kidney disease (DKD) has resulted from the successful employment of systems biology approaches. Systems biology is widely used to comprehensively understand complex human diseases through the unbiased integration of genetic, environmental, and phenotypic aspects of the disease with the functional and structural manifestations of the disease. The application of a systems biology approach to DRD may help to clarify the molecular basis of the disease and its progression. Acquiring this type of information might enable the development of personalized treatment approaches, with the goal of discovering new therapies targeted to an individual’s specific DRD pathophysiology and phenotype. Furthermore, recent efforts have revealed shared and distinct pathways and molecular targets of DRD and DKD, highlighting the complex pathophysiology of these diseases and raising the possibility of therapeutics beneficial to both organs. The objective of this review is to survey the current understanding of DRD pathophysiology and to demonstrate the investigative approaches currently applied to DKD that could promote a more thorough understanding of the structure, function, and progression of DRD.


2018 ◽  
Vol 33 (11) ◽  
pp. 1950-1959 ◽  
Author(s):  
Katherine R Tuttle ◽  
Frank C Brosius ◽  
Sharon G Adler ◽  
Matthias Kretzler ◽  
Ravindra L Mehta ◽  
...  

2018 ◽  
Vol 20 ◽  
pp. 6-13 ◽  
Author(s):  
Skander Mulder ◽  
Habib Hamidi ◽  
Matthias Kretzler ◽  
Wenjun Ju

2010 ◽  
Vol 5 (1) ◽  
pp. 127-135
Author(s):  
Satish P RamachandraRao ◽  
Priti Talwar ◽  
Timothy Ravasi ◽  
Kumar Sharma

BMJ Open ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. e042686
Author(s):  
Kam Wa Chan ◽  
Alfred Siu Kei Kwong ◽  
Pun Nang Tsui ◽  
Simon Chi Yuen Cheung ◽  
Gary Chi Wang Chan ◽  
...  

IntroductionDiabetic kidney disease (DKD) is a prevalent and costly complication of diabetes with limited therapeutic options, being the leading cause of end-stage kidney disease in most developed regions. Recent big data studies showed that add-on Chinese medicine (CM) led to a reduced risk of end-stage kidney disease and mortality among patients with chronic kidney disease (CKD) and diabetes. Astragalus, commonly known as huang-qi, is the most prescribed CM or used dietary herb in China for diabetes and DKD. In vivo and in vitro studies showed that astragalus ameliorated podocyte apoptosis, foot process effacement, mesangial expansion, glomerulosclerosis and interstitial fibrosis. Nevertheless, the clinical effect of astragalus remains uncharacterised. This pragmatic clinical trial aims to evaluate the effectiveness of add-on astragalus in patients with type 2 diabetes, stage 2–3 CKD and macroalbuminuria, and to identify related response predictors.Methods and analysisThis is an add-on, assessor-blind, parallel, pragmatic randomised controlled clinical trial. 118 patients diagnosed with DKD will be recruited and randomised 1:1 to receive 48 weeks of add-on astragalus or standard medical care. Primary endpoints are the changes in estimated glomerular filtration rate and urine albumin-to-creatinine ratio between baseline and treatment endpoint. Secondary endpoints include adverse events, fasting blood glucose, glycated haemoglobin, lipids and other biomarkers. Adverse events are monitored through self-complete questionnaire and clinical visits. Outcomes will be analysed by regression models. Subgroup and sensitivity analyses will be conducted for different epidemiological subgroups and statistical analyses. Enrolment started in July 2018.Ethics and disseminationThis study was approved by the Institutional Review Board of the University of Hong Kong/Hospital Authority Hong Kong West/East/Kowloon Central clusters (UW 16-553/HKEC-2019-026/REC (KC/KE)-19-0049/ER-4). We will report the findings in medical journals and conferences. The dataset will be available on reasonable request.Trial registration numberNCT03535935


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