The USFDA has approved Navidea Biopharmaceuticals’ Supplemental New Drug Application (sNDA) for the expanded use of Lymphoseek (technetium Tc 99m tilmanocept) Injection « New Drug Approvals:
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Tracks information on drugs on worldwide basis by Dr Anthony Melvin Crasto, helping millions with websites, 9 million hits on google, 2.5 lakh connections worldwide, P.S. : The views expressed are my personal and in no-way suggest the views of the professional body or the company that I represent.
Wednesday, 18 June 2014
The USFDA has approved Navidea Biopharmaceuticals’ Supplemental New Drug Application (sNDA) for the expanded use of Lymphoseek (technetium Tc 99m tilmanocept) Injection « New Drug Approvals
Tuesday, 17 June 2014
Pharmaceutical co-crystals – are we there yet?
In the pharmaceutical arena it is agreed that co-crystals form a vital part of the solid-state toolbox, allowing the progression of novel compounds through the development pathway to patients and improving properties in older medicines. Sadly though, few co-crystals have made it to the market in the form of a new licensed product. This displays a disconnect between research effort and end product. For some time now it has been possible to determine the formation of co-crystals, by a variety of screening and analytical means; although it is recognised that there will always be phases that sit in the ‘greyer’ area of the salt-co-crystal continuum. It is also possible, with limitations, to predict the formation of co-crystals in silico via energetic and structural considerations. So what are the major hurdles and missing links, and what are the key structural properties we need to study to improve the success rate? This highlight hopes to address these.
http://pubs.rsc.org/en/Content/ArticleLanding/2014/CE/C4CE00127C?utm_medium=email&utm_campaign=pub-CE-vol-16-issue-26&utm_source=toc-alert#!divAbstract
Pharmaceutical co-crystals – are we there yet?
Show Affiliations
H
*Corresponding authors
a School of Pharmacy, University of Lincoln, Brayford Pool, Lincolnshire, Lincoln, UK
bChemistry, University of Southampton, Highfield, Southampton, UK
cSchool of Medicine, Pharmacy and Health (Pharmacy), Durham University, Wolfson Building, F111, Queen's Campus, Stockton on Tees, UK
E-mail: d.J.berry@durham.ac.uk
E-mail: d.J.berry@durham.ac.uk
CrystEngComm, 2014,16, 5753-5761
DOI: 10.1039/C4CE00127C
Monday, 16 June 2014
Thursday, 12 June 2014
R&D productivity: Drug approvals don’t tell the whole story
By Zachary Brennan, 28-May-2014
As the number of drug approvals declined
between 2012 and 2013 by more than 30%, the value of new therapeutic
agent approvals seems to indicate a stronger year than initially
thought.
New method for uncovering side effects before a drug hits the market
New method for uncovering side effects before a drug hits the market
http://www.sciencedaily.com/releases/2013/01/130102140516.htm
Side
effects are a major reason that drugs are taken off the market and a
major reason why patients stop taking their medications, but scientists
are now reporting the development of a new way to predict those adverse
reactions ahead of time. The report on the method, which could save
patients from severe side effects and save drug companies time and
money, appears in ACS' Journal of Chemical Information and Modeling.
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