Foundation Medicine Inc. (NASDAQ:FMI)

Michael Scally MD

Doctor of Medicine
10+ Year Member
Foundation Medicine Inc. (NASDAQ:FMI)
Foundation Medicine
https://www.google.com/finance?q=NASDAQ:FMI
https://finance.yahoo.com/q?s=FMI


Cancer diagnostics company Foundation Medicine files for a $86 million IPO
7/29/13

Foundation Medicine, which develops diagnostic systems that assess genomic alterations in cancer cells and match patients with targeted therapies, filed on Monday with the SEC to raise up to $86 million in an initial public offering. The Cambridge, MA-based company, which was founded in 2009 and booked $15 million in sales for the 12 months ended March 31, 2013, plans to list on the NASDAQ under the symbol FMI. Foundation Medicine initially filed confidentially on June 24, 2013. Goldman Sachs, J.P. Morgan, Leerink Swann and Sanford Bernstein are the joint bookrunners on the deal. No pricing terms were disclosed.

http://www.renaissancecapital.com/ipohome/news/Cancer-diagnostics-company-Foundation-Medicine-files-for-a-$86-million-IPO-15373.html


Foundation Medicine seeks $86.3M IPO amid chase for reimbursement
UPDATED: Foundation Medicine seeks $86.3M IPO amid chase for reimbursement - FierceBiotech

S-1... Form S-1


Report... Foundation Medicine – 2012 Fierce 15
Foundation Medicine – 2012 Fierce 15 - FierceBiotech


Celgene-backed Agios and Foundation partner in breakthrough cancer strategy
Celgene-backed Agios and Foundation partner in breakthrough cancer strategy - FierceBiotech

July 29, 2013 | By Ryan McBride

Foundation Medicine has bought a ticket to ride the IPO train. The Cambridge, MA-based company, which provides genomic tests for cancer patients and drug researchers, has proposed an $86.3 million initial public offering. There have been nearly 30 maiden public offerings in biotech, and the company follows several cancer-focused startups that have completed successful deals.

Foundation operates on the cutting edge of personalized cancer treatment, but sometimes being way ahead of the curve comes with costs. As the company's filing on Monday states, the company has not yet begun to seek reimbursement for its clinical FoundationOne tests for cancer patients on Medicare. And the company indicated some uncertainties about gaining reimbursement for the test in the SEC filing for the public debut.

In fact, the venture-backed company has made most of its money from a growing list of drug developers that use its testing services to advance targeted treatments against tumors. There are 18 biopharma companies on Foundation's list of research partners, including industry giants such as Johnson & Johnson ($JNJ), Novartis ($NVS) and Sanofi ($SNY). In 2012 the company scored $8 million of its $10.6 million in revenue from biotech and pharma groups, compared with $2.6 million from FoundationOne sales.

The company, a 2012 Fierce 15 winner, is growing rapidly this year. It pulled in revenue of $5.2 million and a net loss of $7.3 million in the first quarter of 2013 compared with revenue of $612,000 and a $5.4 million net loss in the same three-month period a year earlier. The surge in revenue follows the June 2012 launch of FoundationOne, a next-generation sequencing test that assesses 236 cancer-related genes in cancer patients, helping to match them with appropriate treatments.

More than 1,500 doctors have ordered the test since its market debut, the company said. And Foundation boasts a lineup of big-named investors such as Microsoft ($MSFT) Chairman Bill Gates, Google Ventures, Kleiner Perkins Caufield & Byers and founding backer Third Rock Ventures. Foundation, formed in 2009, could be the third company from Third Rock to pull off an IPO this year after the Boston-based venture firm's portfolio companies bluebird bio ($BLUE) and Agios Pharmaceuticals ($AGIO) both went public within the last several weeks. (Agios CEO David Schenkein is also on the board of Foundation, which lists Agios among its biopharma partners.)

If Foundation can overcome reimbursement hurdles, the company could become a major player in the global diagnostics market. Yet the SEC filing indicates that so far the company owes most of its commercial success to biopharma companies.
 
Bank of America Merrill Lynch 2014 Healthcare Conference
http://www.veracast.com/webcasts/baml/healthcare2014/id34108152516.cfm
http://www.veracast.com/webcasts/baml/healthcare2014/events/1091_founda/pdf/Foundation_Medicine_Inc.pdf
 
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Are you front running Doc[:o)] seriously this is a pick up nice nice pick up here. Short interest peaked in march At just above 3 mil now coming back down to around 2.1 mill as 4/30 and I am guessing with the recent sell off it is now lower. It has to be close to a cover and any sort of rally we will see a quick cover in here and a nice bounce to roll with it. ASCO could be the excuse to cover????? Thanks for the show doc wasn't on my radar.
 
Closed out half my position yesterday. I can't help it I am a trader/manager and the trader part of me negotiated with the manager part and I sold half.
 
Option trading is my hobby and has been since the old Wade B Cook days... Made a lot and lost a lot (thanks to the Brazilian currency floating that year and the last week of my options expirations)... Loved the days Amazon could do 100 dollar day swings lol and how you could trade AOL every time it did a stock split and you could bank on it... oh man wish I had a lot of investment cash then as I would have retired that year lmao... Kinda hard to trade when your in the military though lmao...

FMI trading at the 24 dollar range all day, very nice... But being an option man I cant make any money here right now but those that have the money to trade the stock you could do nice watching this stock... Now I just speculate and do paper trades since Im back home just to get my knack back... I did paper trade 1500.00 to 15k in 3 months though and now I could kick myself for not pulling the trigger lol....

VolTrader,

I would like to hear more from you... I do like your style... Remember I don't have the cash to trade many of the stocks but I will be trading options most definitely so please keep us (being selfish, at least keep me up lol) on what I need to be looking at when you here (edit not here but hear lol) it....

BBB
 
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Also wanted to thank you Michael for the information and make sure you too keep us informed on great news like this... Just wished I could have invested like Voltrader did I was so excited about this one and still am just wish the options had a bit more interests...

Oh and again Voltrader I am by no means even remotely comparable to your knowledge so Im sure others and myself would love to keep hearing from you!!!!

BBB
 
Ha I have just been around for a while BBB. FMI options market you can dive a truck through so no it is not a good option candidate because of the illiquid nature. I play options all the time but I stick to QQQ and the SPY for that. Been on vacay so I will be back in the groove mañana.
Yes the good Dr. has in incredible resources and tools for research in the Biotech arena all public info he just has ways to filter. So believe or not I always keep up with his posts in here sometimes he awakens me to a gem. As always thanks Doc.
 
FMI—Leading academic centers ask FDA not to regulate laboratory-developed tests:
http://www.aruplab.com/AboutARUP/PressRoom/PressRelease/2014/Letter%20to%20OMD%20from%20Lab%20Leaders.pdf
 
F.D.A. Moves to Regulate Lab-Developed Tests
http://www.nytimes.com/2014/08/01/business/fda-to-regulate-lab-developed-test-kits.html


Today, the U.S. Food and Drug Administration took important steps to ensure that certain tests used by health care professionals to help diagnose and treat patients provide accurate, consistent and reliable results.

First, the FDA is issuing a final guidance on the development, review and approval or clearance of companion diagnostics, which are tests used to identify patients who will benefit from or be harmed by treatment with a certain drug. Companion diagnostic tests are intended to aid physicians in selecting appropriate therapies for individual patients. These tests are commonly used to detect certain types of gene-based cancers.

Second, consistent with the requirements of the Food and Drug Administration Safety and Innovation Act of 2012 (FDASIA), the agency is notifying Congress of its intention to publish a proposed risk-based oversight framework for laboratory developed tests (LDTs), which are designed, manufactured and used within a single laboratory. They include some genetic tests and tests that are used by health care professionals to guide medical treatment for their patients.


 
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