Get 40% Off
🚨 Volatile Markets? Find Hidden Gems for Serious OutperformanceFind Stocks Now

Foamix IPO: Large Market, Good Trial Results, Neutral Rating

Published 09/18/2014, 12:59 AM
Updated 07/09/2023, 06:31 AM

Foamix Ltd. (FOMX) -- new IPO scheduled for Thursday, Sept. 18, 2014.  The full IPO calendar is available at IPOpremium.
 
Overview
FOMX is a clinical-stage specialty pharmaceutical company focused on developing and commercializing its proprietary minocycline foam for the treatment of acne, impetigo and other skin conditions. Based on clinical trials, FOMX believes that FMX101 has the potential to become the new standard of care for the moderate-to-severe acne market. The P/E ratio is -62, which indicates a low cash burn rate relative to the market cap.
 
Based in Rehovot, Israel, Foamix Ltd. (FOMX) scheduled a $65 million IPO on the NASDAQ with a market capitalization of $234 million at a price range midpoint of $11 for Thursday September 18, 2014.
 
SEC Documents   Manager, Co-Managers: Barclays, Cowen & Company
Joint Managers: Oppenheimer & Co., Maxim Group LLC
 
Conclusion:

  • The rating on FOMX is neutral
  • Large acne market, Encouraging clinical trial results
  • License agreements with Bayer AG (Intendis), Merz Pharmaceuticals, LLC and Actavis
  • Low cash burn rate relative to market cap

 
Valuation
Glossary
 
Valuation Ratios:
Mrkt Cap ($mm)  $220
Price /Sls  366.7
Price /Erngs  -62.1
Price /BkVlue  3.3
Price /TanBV  3.2
% offered in IPO  5%

 
To put the conclusions and observations in context, the following is reorganized, edited and summarized from the full S-1 referenced above.
 
Business
FOMX is a clinical-stage specialty pharmaceutical company focused on developing and commercializing its proprietary minocycline foam for the treatment of acne, impetigo and other skin conditions.
 
Market
According to the American Academy of Dermatology, acne affects approximately 40 to 50 million people in the U.S. alone, approximately 10 million of whom suffer from moderate-to-severe acne according to the Journal of Investigative Dermatology.
 
The U.S. market for branded prescription drugs for acne was estimated to be approximately $2.6 billion for the 12 months ended March 31, 2014, of which $1.0 billion was attributed to oral antibiotics such as Solodyn, the current standard of care for moderate-to-severe acne, and the remaining $1.6 billion was attributed to topical drugs such as Epiduo and Aczone, which are used to treat mild acne.
 
Technology platform
FOMX developed FMX101 and FMX102 using its proprietary technology, which includes its foam-based platforms.
 
This technology enables FOMX to formulate and stabilize a wide variety of drugs and deliver them directly to their target site.
 
FOMX’s foam platforms have significant advantages over alternative delivery options and are suitable for multiple application sites, creating a potential pipeline of products across a range of conditions to drive future growth.
 
Lead product candidates & clinical trials
FOMX’s lead product candidates, FMX101 for moderate-to-severe acne and FMX102 for impetigo, are novel topical foam formulations of the antibiotic minocycline. FOMX’s clinically and statistically significant Phase II clinical trial results demonstrate that FOMX’s minocycline foam, FMX101, provides a faster, more effective treatment than the reported results for oral minocycline, the current standard of care for moderate-to-severe acne, and does so with fewer side effects.
 
Based on these results, FOMX believes that FMX101 has the potential to become the new standard of care for the moderate-to-severe acne market.
 
FMX101 for moderate-to-severe acne.   
FMX101, a 4% minocycline foam formulation for moderate-to-severe acne, is its lead product candidate.
 
In 2013, FOMX completed a dose-ranging Phase II clinical trial of FMX101 in Israel, involving 150 patients aged 12 to 25 with moderate-to-severe acne.
 
This trial demonstrated both clinically and statistically significant efficacy versus the control placebo group, with FMX101 reducing inflammatory acne lesions by 71% in only six weeks and non-inflammatory lesions by 73% in 12 weeks. In addition, no drug-related systemic side effects were observed.
 
Phase II clinical trial for FMX102
FOMX has also completed a Phase II clinical trial for FMX102, and based on its efficacy and safety profile, FOMX believes it will present an attractive option for the treatment of impetigo, including impetigo caused by methicillin-resistant staphylococcus aureus, or MRSA.
 
FOMX expects to commence pivotal Phase III clinical trials for both product candidates in 2015.
 
License agreements
In addition, FOMX has entered into development and license agreements relating to its technology with various pharmaceutical companies such as Bayer AG NA (XETRA:BAYGN) (Intendis), Merz Pharmaceuticals, LLC and Actavis Inc (NYSE:ACT), which, from FOMX’s inception to June 30, 2014, have generated approximately $14.7 million in revenues.
 
The agreements may entitle FOMX to an additional aggregate amount of up to approximately $30 million in contingent payments if certain conditions are met.
 
FOMX is further entitled to royalties from net sales of the licensed products (or, in certain cases, from net profits generated by them) if they are approved for marketing by the relevant regulatory authorities and commercialized by the licensees.
 
Dividend Policy
No dividends are planned.
 
Intellectual Property
FOMX’s most important patent is its U.S. patent relating to its lead product candidates, FMX101, FMX102 and FDX104, which is expected to remain in effect until 2030.
 
This patent comprises a claim to a formulation of a tetracycline antibiotic which can include minocycline or doxycycline.
 
FOMX’s other patents granted in the U.S. have claims relating to certain formulations of its foam platforms and other technology, including emulsion foams, hydrophobic foams and aqueous foams.
 
As of August 31, 2014, FOMX’s continuous effort in protecting and fortifying its unique intellectual property has yielded a patent portfolio of 70 granted patents in certain countries worldwide, including 31 granted patents in the U.S.
 
Additionally, as of August 31, 2014, FOMX had 114 pending patent applications worldwide, of which 60 are pending in the U.S. describing and claiming its multiple foam based platforms and other technology.
 
FOMX has several composition of matter patent applications pending in relation to FMX101, FMX102 and FDX104 in the U.S. as well as one pending in each of the following international markets, Australia, Brazil, Canada, China, the European Union, India, Israel and Mexico. FOMX’s other pending applications relate to various foam platforms such as emulsion foam, hydrophobic foam, hydro-alcoholic foam and water-free foams, as well as specialty foams (such as potent solvent foams) and FOMX’s recently-developed ‘metered dose dispenser’ for controllable dosing.
 
Competition
As more companies develop new intellectual property in FOMX’s markets, the possibility of a competitor acquiring patent or other rights that may limit FOMX’s products or potential products increases, which could lead to litigation.
 
In addition, FOMX faces competition from the current standard of care.
 
The current standard of care for moderate-to-severe acne includes oral antibiotic drugs such as Solodyn, Doryx, Dynacin and Minocin, in which minocycline or doxycycline are the active ingredients, occasionally in combination with topical anti-acne drugs such as Acanya, Aczone, Ziana, Epiduo, Benzaclin and Differin.
 
The current standard of care for impetigo is the topical agent Bactroban, with Altabax being the most recently approved topical agent for such indication.
 
The active ingredients in Bactroban and Altabax are the antibiotics mupirocin and retapamulin, respectively.
 
The standard of care for moderate-to-severe rosacea are oral minocycline and doxycycline drugs such as Oracea, the most recently approved oral doxycycline drug for rosacea.
 
The standard of care for milder cases of rosacea are topical drugs such as MetroGel and Finacea.
 
However, based on its clinical trials, FOMX believes that FMX101 and FMX102 have competitive advantages over the current alternatives and have significantly less adverse side effects.
 
5% stockholders
Tamarkin Medical Innovation Ltd. 21.1%
Meir Eini Holdings Ltd. 21.5%
Amos and Daughters Investments and Properties Ltd. 12.1%
Benny Shabtai  9.4%
Rosa Alba Commerce & Investments Ltd. 7.4%
Amiram Bornstein 6.7%
Doron Freidman 5.7%
                       
Use of proceeds
FOMX intends to use the $58 million in proceeds from its IPO as follows:
 
$20&ndash%

3rd party Ad. Not an offer or recommendation by Investing.com. See disclosure here or remove ads .

Latest comments

Risk Disclosure: Trading in financial instruments and/or cryptocurrencies involves high risks including the risk of losing some, or all, of your investment amount, and may not be suitable for all investors. Prices of cryptocurrencies are extremely volatile and may be affected by external factors such as financial, regulatory or political events. Trading on margin increases the financial risks.
Before deciding to trade in financial instrument or cryptocurrencies you should be fully informed of the risks and costs associated with trading the financial markets, carefully consider your investment objectives, level of experience, and risk appetite, and seek professional advice where needed.
Fusion Media would like to remind you that the data contained in this website is not necessarily real-time nor accurate. The data and prices on the website are not necessarily provided by any market or exchange, but may be provided by market makers, and so prices may not be accurate and may differ from the actual price at any given market, meaning prices are indicative and not appropriate for trading purposes. Fusion Media and any provider of the data contained in this website will not accept liability for any loss or damage as a result of your trading, or your reliance on the information contained within this website.
It is prohibited to use, store, reproduce, display, modify, transmit or distribute the data contained in this website without the explicit prior written permission of Fusion Media and/or the data provider. All intellectual property rights are reserved by the providers and/or the exchange providing the data contained in this website.
Fusion Media may be compensated by the advertisers that appear on the website, based on your interaction with the advertisements or advertisers.
© 2007-2024 - Fusion Media Limited. All Rights Reserved.