Assessing Youth Risk Behavior in a Clinical Trial Setting: Lessons From the Infant Health and Development Program

2010 ◽  
Vol 46 (5) ◽  
pp. 429-436 ◽  
Author(s):  
Elizabeth R. Woods ◽  
Stephen L. Buka ◽  
Camilia R. Martin ◽  
Mikhail Salganik ◽  
Mary Beth Howard ◽  
...  
2011 ◽  
Vol 7 ◽  
pp. S713-S713
Author(s):  
Luc Bracoud ◽  
Angelika Caputo ◽  
Chahin Pachai ◽  
Boubakeur Belaroussi ◽  
Ana Graf ◽  
...  

PEDIATRICS ◽  
1993 ◽  
Vol 92 (1) ◽  
pp. 190-190

"Risk Factors and Outcomes for Failure to Thrive in Low Birth Weight Preterm Infants," by Kelleher et al, was published in the May issue of Pediatrics (1993;91:941-948). The acknowledgments that follow should have appeared at the end of that text: The Infant Health and Development Program is supported by grants to the Department of Pediatrics, Stanford University; The Frank Porter Graham Child Development Center, University of North Carolina; and the eight participating universities by the Robert Wood Johnson Foundation. Additional support was provided to the Department of Pediatrics, Stanford University, from the Pew Charitable Trusts; the Bureau of Maternal and Child Health and Resources Development, Health Resources Services Administration, United States Public Health Service, Department of Health and Human Services (grant MCJ-060515); and the Stanford Center for the Study of Families, Children and Youth.


Author(s):  
Marta de-Melo-Diogo ◽  
Jorge Tavares ◽  
Ângelo Nunes Luís

Blockchain technology in a clinical trial setting is a valuable asset due to decentralization, immutability, transparency, and traceability features. For this chapter, a literature review was conducted to map the current utilization of blockchain systems in clinical trials, particularly data security managing systems and their characteristics, such as applicability, interests of use, limitations, and issues. The advantages of data security are producing a more transparent and tamper-proof clinical trial by providing accurate, validated data, therefore producing a more reliable and credible clinical trial. On the other hand, data integrity is a critical issue since data obtained from trials are not instantly made public to all participants. Work needs to be done to establish the significant implications in security data when applying blockchain technology in a real-world clinical trial setting and generalized conditions of use to establish its security.


2019 ◽  
Vol 188 (3) ◽  
pp. 394-403 ◽  
Author(s):  
Jithma P. Abeykoon ◽  
Saurabh Zanwar ◽  
Stephen M. Ansell ◽  
Morie A. Gertz ◽  
Shaji Kumar ◽  
...  

2017 ◽  
Vol 1 (Suppl) ◽  
pp. 23-25
Author(s):  
Najibah A. Galadanci ◽  
Shehu U. Abdullahi ◽  
Leah D. Vance ◽  
Musa A. Tabari ◽  
Shehi Abubakar ◽  
...  

2012 ◽  
Vol 30 (4_suppl) ◽  
pp. 313-313 ◽  
Author(s):  
Jason Edward Faris ◽  
Theodore S. Hong ◽  
Shaunagh McDermott ◽  
Alexander R Guimaraes ◽  
Dushyant Sahani ◽  
...  

313 Background: The recently published Phase III trial of 5-FU, leucovorin, irinotecan, and oxaliplatin (FOLFIRINOX) demonstrated improved survival compared to gemcitabine in good performance status (PS) patients with metastatic pancreatic cancer (Conroy et al, NEJM 2011). Less is known about the efficacy and tolerability with FOLFIRINOX in the non-clinical trial setting. In this retrospective analysis, we report our institutional experience with FOLFIRINOX. Methods: 29 patients with locally advanced or metastatic pancreatic cancer treated with FOLFIRINOX between July 2010 and April 2011 were used for this analysis. Clinical characteristics, and gradeable toxicities were tabulated, and formal radiographic review performed to determine best overall response rates (ORR). Results: 17 patients received FOLFIRINOX for metastatic disease and 12 patients for locally advanced disease. The median age of patients was 60 (range 39-76). 22/29 patients were men. 18/29 patients had received no prior chemotherapy. There was one patient with PS 2; all others had PS 0 or 1. 8/29 patients had biliary stents. Overall, 11 partial responses (PR) were observed (ORR 38%); 10/11 partial responses were in chemo-naïve patients, who had an ORR of 56%. In the metastatic setting, there were 6 PR, for an ORR of 35%, and 7 patients with stable disease (SD). In the locally advanced setting, there were 5 PR (ORR 42%), and 7 patients with SD. Following treatment with FOLFIRINOX, one patient with locally advanced disease has subsequently undergone R0 resection. The median number of cycles performed was 8 in both the locally advanced and metastatic settings. 12/29 patients required an ED visit or hospitalization during treatment. Grade 3/4 neutropenia was observed in 10 patients; 7/10 had not received prophylactic growth factor treatment from the start of FOLFIRINOX. 4 patients developed febrile neutropenia, 4 patients developed grade 3/4 thrombocytopenia, and 1 patient developed grade 4 anemia. Conclusions: In a non-clinical trial setting, FOLFIRINOX demonstrated activity in both the metastatic and locally-advanced settings. FOLFIRINOX appears to be associated with manageable, but significant toxicities, with over 40% of patients requiring hospitalization.


2009 ◽  
Vol 22 (3) ◽  
pp. 263-266 ◽  
Author(s):  
Yong Ma ◽  
Marinella Temprosa ◽  
Sarah Fowler ◽  
Ronald J. Prineas ◽  
Maria G. Montez ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document