
Тearly 75 million Americans suffer from seasonal allergies, including those related to trees and tree pollen. Tree allergies can be difficult to combat since trees emit a large amount of pollen over a wide area. They typically start to produce pollen as early as January in the southern United States or as late as May in the northern part of the country.
Friday, August 28, 2015
Cancer CD Antigens Inhibitors Therapy Market & Pipeline Insight 2015
DUBLIN--(BUSINESS WIRE)--Research and Markets (.researchandmarkets.com/research/tb22l6/cancer_cd)
has announced the addition of the "Cancer
CD Antigens Inhibitors Therapy Market & Pipeline Insight 2015"
report to their offering.
Pharmaceutical companies are continuously looking for better therapeutic
options to effectively cure and prevent various malignancies. Buy Skelaxin (Metaxalone Mr) with free prescription Several
options for cancer treatment are available belonging to various classes
of molecules. About Diflucan (Fluconazole) with free prescription Different types of cancer have different
pathophysiological characteristics due to which distinctive approach is
required for effective treatment. About Sumycin (Tetracycline) Several molecules have been discovered
out of which CD antigens have been found to play an important role in
cancer progression and proliferation. Enapril without prescription Investigators are trying to assign
different functions to CD antigens by doing extensive research and
development. Prograf (Tacrolimus) with no prescription Their role in cancer development has been noted due to
which lots of progress would be observed in this segment. Buy Bacopin online Most of the
work has been done in cancer segment and pharmacological profiles are
expected to be improved in coming years.
CD antigen cancer therapeutics have diverse design and target due to
which they could be used for several malignancies. http://anti-infectives-opinion.blogspot.com Presence of BiTEs,
ADC, monoclonal antibodies and tri-functional antibodies for targeting
different CD antigens has been commercialized. Next step is assumed to
be the improvement in design as complexity at molecular levels makes it
difficult to manufacture them in large quantities. This issue not only
decreases the productivity but also increases the cost of production.
Higher cost of end products limits the number of cancer patients
choosing them as a part of their regular therapeutic regime. With the
use of advanced technology it is expected that this issue would be
overcome in coming years. Some of the progress could be observed in case
of monoclonal antibodies and same scenario could be observed for other
CD antigen cancer therapeutics in coming years.
Clinical trials are being instigated across the globe in order to extend
their utilities in different malignancies. They are versatile in nature
due to which they could be used as a part of combinatorial therapy along
with monoclonal antibodies. Their utilities in different malignancies
are also being studied but results of such clinical trials remains
elusive. They have strong clinical pipeline due to which several
products would be introduced in coming years. However, these products
are at different stages of clinical pipeline and they may take long
winding times as lots of experiments proving their safety and efficacy
has to be done. With time more CD antigens are expected to be discovered
and they would help in the increased market size. Commercial success of
marketed CD antigen cancer therapeutics shows that they would be
generating significant revenues in coming years.
CD antigen cancer market is expected to witness introduction of several
products which will help the pharmaceutical companies to generate
significant revenues. Increasing demand for better therapeutics, large
unmet medical necessities and large numbers of cancer patient s patient
are expected to be responsible for the growth of this market segment.
Increased funding in research and development along with utilization of
advanced technology will also help in increasing their market shares
across the globe. Numerous innovative CD antigen cancer therapeutics are
at different stages of clinical trials which would increase their market
shares. Despite these facts they have higher prices and their
manufacturing is difficult but utilization of advanced technology along
with streamlining of various processes are expected to overcome this
barrier. In this way, future of CD antigen cancer therapeutics looks
optimistic due to their superior pharmacological profiles.
CD Antigens Segments in Report:
CD3, CD4, CD9, CD11, CD19, CD20, CD22, CD26, CD27, CD28, CD29, CD33,
CD37, CD40, CD44, CD45, CD47, CD52, CD55, CD56, CD66, CD70, CD74, CD80,
CD95, CD98, CD100, CD117, CD135, CD137, CD152, CD200, CD223, CD227,
CD246, CD248, CD274, CD276, CD279
Cancer CD Antigens Inhibitors Therapy Market & Pipeline Insight 2015
Report Highlight:
- Nomenclature & Classification of CD Antigens
- Mechanism of CD Antigen Cancer Therapeutics
- Cancer CD Antigen Therapy Market Overview
- Cancer CD Antigen Inhibitors Clinical Pipeline by Company, Indication
& Phase
- Cancer CD Antigen Inhibitors Clinical Pipeline: 207 Drugs
- Marketed Cancer CD Antigen Inhibitors: 27 Drugs
- Majority of Cancer CD Antigen Inhibitors in Preclinical Phase: 70 Drugs
- Cancer CD Antigens Clinical Pipeline Dominated by CD20 Antigen: 44
Drugs
- Cancer CD Antigens Clinical Pipeline is Represented in 52 Graphs &
Charts
Companies Mentioned
- ARIAD Pharmaceuticals
- AXXO
- Alexion Pharmaceuticals
- AryoGen Biopharma
- Bayer HealthCare
- Biocad
- Biogen
- Biotecnol Inc.
- Bristol-Myers Squibb
- Chugai Pharmaceutical
- Dr Reddy s Laboratories
- Eisai Co Ltd
- Emergent BioSolutions
- Genmab
- ImmunoGen
- Intas Biopharmaceuticals
- MacroGenics
- MedImmune
- Merck
- Novartis
- Ono Pharmaceutical
- Onyx Pharmaceuticals
- PROBIOMED
- Pfizer
- Roche
- UCB
- Xencor
For more information visit .researchandmarkets.com/research/tb22l6/cancer_cd

Wednesday, August 19, 2015
CHMP recommends label update for Giotrif® with addition of data demonstrating overall survival benefit for patients with EGFR mutation-positive lung cancer
INGELHEIM, Germany--(BUSINESS WIRE)--Boehringer Ingelheim today announced that the Committee for Medicinal
Products for Human Use (CHMP) of the European Medicines Agency (EMA) has
issued a positive opinion for an update to the European label for Giotrif®
(afatinib*), strengthening and broadening the efficacy profile based on
additional Phase III data. About Rheumatrex (Methotrexate) with free prescription The CHMP recommendation includes data from
the LUX-Lung 3 and 6 trials which showed patients whose tumours have the
most common EGFR mutation (deletion in exon 19; del19) lived more than
one year longer when treated with first-line Giotrif®
compared to standard chemotherapy (overall survival; OS = secondary
endpoint, progression-free survival; PFS = primary endpoint).
Dr. Elocon (Mometasone) without prescription Mehdi Shahidi, Medical Head, Solid Tumour Oncology, Boehringer
Ingelheim commented, “This update to the European label reinforces the
importance of Giotrif® as a targeted treatment for patients
with EGFR mutation-positive NSCLC, especially for those whose tumours
harbor the most common mutation, del19. About Macrobid (nitrofurantoin monohydrate) with no Rx Giotrif® is the first
and only targeted agent to date to have shown an overall survival
benefit for these patients in the first-line setting.”
Following CHMP positive opinion, the European prescribing information
will now be updated to include additional data from LUX-Lung 3 and
LUX-Lung 6. Eldepryl with no Rx Both studies met the primary endpoint of PFS for patients
whose tumours have common EGFR mutations receiving first-line Giotrif®. Retin-A (Tretinoin) with free prescription
In addition to new OS data, updated PFS data from the two trials will
also be reflected in the updated European label, as will the significant
improvements in lung cancer-related symptoms (cough, shortness of
breath, pain) and quality of life observed with Giotrif®
compared to chemotherapy.
Adverse events for Giotrif® in the LUX-Lung 3 and 6 trials
were as expected with EGFR inhibition and were predictable, manageable
and reversible. Buy Appetite Suppressants online Diarrhoea and rash/acne were the most
frequently reported side effects with Giotrif® therapy.
NSCLC is the most common form of lung cancer comprising over 85% of lung
cancer cases. http://cardiobloodreview.wordpress.com EGFR mutation-positive NSCLC is a subtype of
lung cancer. EGFR mutations are found in 10-15% of Caucasian and 40% of
Asian patients with NSCLC. There are different types of EGFR mutations;
the most common, which account for 90% of all EGFR mutations being del19
(approx. 50%) and L858R (approx. 40%). Afatinib, an oral,
once daily ErbB family blocker, is currently
approved in more than 60 countries for the first-line treatment of
specific types of EGFR mutation-positive NSCLC (under brand names:
Giotrif® / Gilotrif®).
*Afatinib is approved in a number of markets, including the EU, Japan,
Taiwan and Canada under the brand name GIOTRIF® and in the US
under the brand name GILOTRIF® for use in patients with
specific types of EGFR mutation-positive NSCLC. Registration conditions
differ internationally, please refer to locally approved prescribing
information. Afatinib is under regulatory review by health authorities
in other countries worldwide. Afatinib is not approved in other
indications.
For notes to editors and references, please visit:
.boehringer-ingelheim.com/news/news_releases/press_releases/2015/19_august_2015_oncology.html
Intended audiences:
This press release is issued from our Corporate Headquarters in
Ingelheim, Germany and is intended to provide information about our
global business. Please be aware that information relating to the
approval status and labels of approved products may vary from country to
country, and a country-specific press release on this topic may have
been issued in the countries where we do business.
Further Media Channels
.facebook.com/boehringeringelheim
.twitter.com/Boehringer
.youtube.com/user/boehringeringelheim

Monday, August 17, 2015
China Ribonucleic Acid II (RNAII) for Injection Market Investigation Report 2010-2019
. About Suprax (Cefixime) without Rx DUBLIN--(BUSINESS WIRE)--Research and Markets (.researchandmarkets.com/research/bxl5pl/investigation)
has announced the addition of the "Investigation
Report on China s ribonucleic acid II (RNAII) for Injection, 2010-2019"
report to their offering.
RNAII for injection, one kind of immunomodulator, can improve body
immunity and inhibit tumor by causing vacuolar degeneration and
colliquative necrosis in tumor cells as well as generating large amounts
of hyperplastic fibroblasts, macrophages, lymphocytes or even connective
tissue to substitute tumor tissue. Buy Weight Loss online About Noroxin (Norfloxacin) with no prescription And it is used for the adjuvant
treatment of pancreatic cancer, liver cancer, stomach cancer, breast
cancer, soft tissue sarcoma and other cancers especially hepatitis B. http://allegra-opinion.blogspot.com About Isordil Sublingual (Isosorbide Dinitrate) with no Rx
RNAII for injection can also be used for the treatment of various
diseases caused by low immune function.
According to the market survey, RNAII for injection develops fast in
China with sales value rising from less than CNY 60 million in 2005 to
about CNY 500 million in 2014 and CAGR during this period reaching 80%.
With the lifestyle changes brought about by economic development as well
as the serious environmental pollution, the incidence of cancer keeps
increasing with the number of new cases exceeding 3 million each year in
China. Cycrin (Medroxyprogesterone ) with no prescription Meanwhile, there are over 90 million hepatitis B patients in
China too. Dovonex without prescription Therefore, the market size of RNAII for injection is expected
to keep growing in the next few years in China.
Key Topics Covered:
1 Related Concepts of RNAII for Injection
2 Market Profile of RNAII for Injection in China
3 Survey on Sales Status of RNAII for Injection in China, 2010-2014
4 Survey on Market Share of Major Manufacturers of RNAII for Injection
in China, 2010-2014
5 Survey on Dosage Forms of RNAII for Injection in China, 2010-2014
6 Reference Price of RNAII for Injection in Chinese Hospitals in 2014
7 Major Manufacturers of RNAII for Injection in Chinese Market, 2010-2014
8 Market Outlook of RNAII for Injection in China, 2015-2019
Companies Mentioned
- Jilin Aodong Pharmaceutical Industry Group Yanji Co., Ltd
- Nanjing Xinbai Pharmaceutical Co., Ltd
- Xinxiang Dongsheng Pharmaceutical Co., Ltd
For more information visit .researchandmarkets.com/research/bxl5pl/investigation

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