This month has been quite hectic month for me, at the initial week of the month I had been to Kumbh Mela (A festival which is celebrated after every 12 years in Hindu religion) and then had been to Kolkata (City of Joy) for my birthday and Bengali happy new year celebrations, then came back and had to finish my client project and now I have got time to blog something and I am feeling good about it.
This month there were many updates Abbott billion dollar acquisition and day before yesterday the news was Charles river laboratories is planning to acquire Wuxiapptech, this collaboration will help Charles river penetrate more into the emerging markets thus helping it to develop capabilities in both preclinical and clinical stage services for varied industries which will range from diagnostics, markers, devices, biologics, chemicals and small molecules…..and sometime back while I was analyzing the list of fast developing CRO’s in Asia, Wuxi was contending in the Top 3 slot…………
Thursday, April 29, 2010
Wednesday, April 07, 2010
Pharmaceitical M&A Report- Last 10 years
Today morning was reading a report on Mergers and Acquisitions and in the report it was mentioned that during these last 10 years there were 1, 717 M&A in pharma sector with the disclosed amount of $295 Billion and the biggest players includes
Roche - $46.8 Billion acquisition of Genentech
Astra Zeneca- $15.2 Billion deal for Med Immune
And also included in the list were GlaxoSmithKline, Amgen, Eli lily and company, Genzyme Corporation but the big fish which was missing from the list was our old patron in M&A Pfizer which last year went for the highest M&A deal ever.
Among Top 25 Biotechnology M&A four companies announced multiple acquisitions which includes Glaxo Smith Kline, Amgen Inc., Eli Lilly & Co and Genzyme Corporation and the report stated that most of the acquisitions were from publically traded sellers and buyers
Biotechnology Mergers and Acquisitions, 2000 to 2009
Year Dollars Committed Number Of Deals
2009 $47,523,349,040 193
2008 $93,879,257,347 148
2007 $42,105,127,700 145
2006 $36,407,170,500 115
2005 $23,196,902,050 113
2004 $6,764,873,000 96
2003 $16,681,231,200 128
2002 $3,274,727,708 96
2001 $20,150,840,000 85
2000 $5,076,797,094 52
Totals $295,060,275,639 1,171
In this report they mentioned that only about 18% of the biotechnology companies which were targeted in mergers and acquisitions announced in the span of 10 years ended December 31, 2009 were disclosing their revenues at the time of the M&A announcements.
Out of the top 25 largest biotechnology M&A announced during the 10-year period ended December 31, 2009 most of them were United States-based concern and some were European companies. In Year 2008 -2009 major M&A activity happened in United States preceded by Europe, Canada and Japan
This report also gave information related to Top states in United states with largest M&A activity they include California, New York, Massachusetts, New Jersey, Maryland, Pennsylvania, North Carolina, Washington and Texas.
Outside the U.S., the countries included in the list were Switzerland, Germany, England, Netherlands, Japan, Canada, France, Australia and Denmark.
Seller side point of view it gave additional information about various states with United states having highest number of M&A they include California, Massachusetts, Maryland, New York, New Jersey, Washington, Pennsylvania, North Carolina and Texas.
Link:http://www.kerentech.com/?p=4504
Thursday, April 01, 2010
Biosimilar Market
Some days back I received an email from some lady and she asked me some question related to biosimilars so I thought of jotting them down in my blog
I. What is some of the current challenges you are experiencing in your industry?
•Manufacturing part: Large investment required due to expensive and sensitive manufacturing process with difficulty in reproducibility of results.
•Huge clinical trial development cost
•Regulatory process till now not clearly defined in regulatory market Europe (EMEA) and United states (FDA)
II. What are the top 3 things that should improve?
According to me the following things should improve for dissimilar in Indian scenario they include
•Better clinical studies prioritization and development with expertise in filing in regulated market
•Comprehensive competitive intelligence or due diligence for the product portfolio with establishment of state of the art manufacturing process
•Consistent portfolio strategy with effective branding and marketing skills.
III.What is upcoming future opportunities that you see in the field of biosimilars?
In accordance to indian scenario the oppurtunities associated with biosimilars include
•Cost saving
•Higher margins and better profitability structure as blockbuster drugs are coming off patent.
PS: The 12 years exclusivity for biopharmaceutical drug in United States I don’t see a good market potential of bio similar in United States in the coming decade as compared to European bio similar approvals.
I. What is some of the current challenges you are experiencing in your industry?
•Manufacturing part: Large investment required due to expensive and sensitive manufacturing process with difficulty in reproducibility of results.
•Huge clinical trial development cost
•Regulatory process till now not clearly defined in regulatory market Europe (EMEA) and United states (FDA)
II. What are the top 3 things that should improve?
According to me the following things should improve for dissimilar in Indian scenario they include
•Better clinical studies prioritization and development with expertise in filing in regulated market
•Comprehensive competitive intelligence or due diligence for the product portfolio with establishment of state of the art manufacturing process
•Consistent portfolio strategy with effective branding and marketing skills.
III.What is upcoming future opportunities that you see in the field of biosimilars?
In accordance to indian scenario the oppurtunities associated with biosimilars include
•Cost saving
•Higher margins and better profitability structure as blockbuster drugs are coming off patent.
PS: The 12 years exclusivity for biopharmaceutical drug in United States I don’t see a good market potential of bio similar in United States in the coming decade as compared to European bio similar approvals.
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