Tuesday, December 31, 2013

Zhyve Belarus!!!


Happy New Year! Good luck in 2014!!!

Сталин

Happy new year! LoL


Saturday, December 28, 2013

Top 2012 pharmaceuticals

Targeted failure of the week. Post No 129. AXL1717

Axelar AB (Solna, Sweden) said twice-daily oral AXL1717 missed the primary endpoint of improving the 12-week progression-free survival (PFS) rate vs. docetaxel in the Phase II AXL-003 trial to treat non-small cell lung cancer (NSCLC) (25.9% vs. 39%, p=0.19). AXL1717 also missed the secondary endpoints of improving median overall survival (OS) (7.52 vs. 9.41 months, p=0.91) and PFS (2.83 vs. 2.85 months, p=0.32) vs. docetaxel. Axelar said some early episodes of neutropenia in the AXL1717 arm developed into serious events, some of which were fatal.
In April, Axelar reported interim data from the trial showing that AXL1717 led to a "similar" 12-week PFS rate as docetaxel, but the company declined to disclose details. The open-label, international trial enrolled 99 evaluable patients with previously treated, locally advanced or metastatic NSCLC.
On a conference call to discuss the data, the company said a "rational way forward" would be to evaluate AXL1717 as third-line treatment of NSCLC. Axelar said it is "planning future studies in parallel with ongoing partner discussions," but could not be reached for details. AXL1717 is an oral small molecule insulin-like growth factor-1 (IGF-1) receptor (IGF1R; CD221) inhibitor, though the company said there is evidence that AXL1717 also suppresses tumor cell division by arresting cells in mitosis.
 

Wednesday, December 25, 2013

Drop in UK death rates from cancer

http://www.pharmatimes.com/Article/13-12-24/Research_is_key_to_big_drop_in_UK_cancer_deaths.aspxResearch is the key cause behind the 22% drop in UK death rates from cancer reported between 1990 and 2011, says new research.
In 1990, 220 in every 100,000 people died of cancer ,but this figure fell to 170 per 100,000 in 2011, due to improved knowledge about preventing the disease, surgical techniques, precisely-targeted radiotherapy and more effective drugs all boosting the outcome for patients
 
 
 

Big Pharma's Top 10 Settlements of Shame for 2013

Friday, December 13, 2013

Your Vote Counts: Who Is the Worst Biotech CEO of 2013?

What a nice approach! The next to come should be:

- the worst targeted drug
- the worst Big Pharma Company
- the worst indication (just like bent penis or painful sex)
 

Avastin - bad news again

 
Patients treated with chemotherapy plus trastuzumab (Herceptin) had 92% iDFS with or without the bevacizumab. Subgroup analysis did not identify any group of patients that benefited from the addition of the angiogenesis inhibitor.
 

Saturday, December 7, 2013

Depeche again


Bent penis? 5%of U.S. men are affected! Not a problem anymore!

Post-modern Health problems - not a joke!!!
 
WASHINGTON (AP) -- The Food and Drug Administration on Friday approved the first drug to treat an unusual condition that causes painful, curved erections in men.
The agency said it approved the biotech drug Xiaflex to treat Peyronie's disease, which causes an abnormal bend in the penis during erection. The disease is caused by scar tissue and can lead to pain and other difficulties during sex.
FDA says the injectable drug is the first non-surgical treatment for the disease.
Drugmaker Auxilium Pharmaceuticals estimates 5 percent of U.S. men are affected.  - It sounds like an epidemic!
Xiaflex was previously approved in 2010 to treat a hand disease that interferes with patients' ability to straighten their fingers. The FDA said in its release that Xiaflex is believed to treat Peyronie's disease by breaking down collagen plaque that builds up in the penis and causes the deformity.
The FDA said it is limiting distribution of the drug to certified physicians and health care centers due to serious potential side effects, including injury of the penis. Health care professionals must enroll and complete a training program before prescribing the drug.
The FDA approved Xiaflex for its new use based on two studies of 832 men with Peyronie's disease. Patients received up to eight injections of the drug and were then followed for a year to see if their condition improved. Patients who received the drug reported significantly fewer problems than those who received a dummy injection.
The drug was developed by BioSpecifics Technologies Corp. of Lynbrook, N.Y., and submitted to the FDA by Chesterbrook, Pa.-based Auxilium Pharmaceuticals Inc.
Shares of Auxilium rose $1.80, or 9.3 percent, to $21.13 in afternoon trading. 

Wednesday, December 4, 2013

Ukraine (and Belarus) will be free! The sober point of view!


Authorship For Sale. Why not?

Very interesting Reading:

"There are some authors who don't have much use for their papers after they're published, and they can be transferred to you," a sales agent for a company called Wanfang Huizhi told a Science reporter posing as a scientist. Wanfang Huizhi, the agent explained, acts as an intermediary between researchers with forthcoming papers in good journals and scientists needing to snag publications. The company would sell the title of co–first author on the cancer paper for 90,000 yuan ($14,800). Adding two names—co–first author and co–corresponding author—would run $26,300, with a deposit due upon acceptance and the rest on publication. A purported sales document from Wanfang Huizhi obtained by Science touts the convenience of this kind of arrangement: "You only need to pay attention to your academic research. The heavy labor can be left to us. Our service can help you make progress in your academic path!"

And the $14,800 is not a big deal for serious researchers!