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In our opinion, Teva Pharmaceutical Industries' (
TEVA
) stock price seems to be significantly below intrinsic value, no
matter how conservatively this is calculated.
TEVA is an international pharmaceutical company headquartered in
Petah Tikva, Israel. It specializes in generic and proprietary
pharmaceuticals and active ingredients. It is the largest generic
drug manufacturer and one of the 15 largest pharmaceutical
companies worldwide, with sales of $18.3 billion, net income of
$560 million and a total staff of 40,000 as of December 31,
2011.
Company's History
Teva's DNA is in the generics business, where it focused during the
early part of its history scoring considerable success thanks to
its cost-conscious corporate culture, focus on efficient
operations, advanced technology and an understanding that gains in
scale eventually translate into a cost advantage in this
industry.
Teva expanded rapidly during the last 10 years through a
combination of conservative management and smart acquisitions and
achieved 27% earnings growth rate with return on invested capital
around 20% as of the last reporting period.
Besides generics, Teva increasingly built up its presence in
branded drugs. While not involved in discovery (the identification
of effective new compounds), Teva has acquired existing compounds
frequently taking advantage of its close relationship with top
Israeli scientific institutions, such as the Weitzman Institute. It
is from the latter facility that Teva acquired Copaxone, its top
selling drug for the treatment of multiple sclerosis or MS.
During the last 3 years Teva's stock has been under heavy
pressure due to a number of concerns. First, the regulatory and
competitive environment for the generics business is changing.
Second, Teva's Copaxone franchise is under threat by both generic
manufacturers and alternative new branded drugs. Third, a set of
operational difficulties involving two of Teva's plants has
temporarily reduced sales on certain product lines.
Industry Overview
Macroeconomic outlook
Teva operates in an industry blessed by generally favorable
long-term economic trends. The healthcare sector is expected to
continue to benefit from the aging of the world population (older
people need extra healthcare) and from increasing adoption rates of
western medicine by emerging countries.
The generics segment in particular is also poised to benefit
from tightening government healthcare budgets and from the advent
of biologics. To counter that, however, tightening budgets may also
create pricing pressure on branded drugs, especially in developed
countries undergoing a long deleveraging process.
Competitive Scenario
Teva operates and competes in several industry segments. In
generics, Teva is the market leader, according to [cite source],
followed by Novartis-owned Sandoz (NOVN), Mylan (
MYL
) and others. Thanks to efficient manufacturing, logistics and
scale, Teva is the low cost producer in its industry.
In my opinion, it is also in the best position within the
industry to capture a significant share of the upcoming biologics
market, given its technological leadership in generics and proven
track record to come out with advanced generics quickly.
In branded drugs, Teva is the #11th world's largest
pharmaceutical company. Teva focuses on CNS (central nervous
system), respiratory, women's health and other lines of business.
As customary in this industry, Teva's revenues are protected by
patents and moderately captive customers (more on this later).
A Porter 5-Forces analysis confirms that Teva tends to retain
most of the value generated in its lines of business as both
customers and suppliers have limited bargaining power, substitute
products are few and entry barriers are significant.
Lines of Business
Teva's sales are approximately divided 50/50 between generics
(faster growing at 7.8% expected CAGR) and branded (higher margin).
In 2012 sales are expected to reach $20.5 billion, according to
consensus estimates posted on Teva's website.
Sales originate 50% in the US, roughly 30% in Europe and 20% in
the rest of the world. There is an existing trend, consistent with
the management's stated strategy, to increase the share of sales
coming from emerging markets. About 4% of sales derive from the
over-the-counter market, thanks to a recent partnership with
Procter & Gamble (
PG
) (we expect this share to increase in the future).
Outstanding issues
Overview
Teva's share price has been recently hovering around $40,
approximately the price it was trading at in 2005. Considering that
between 2005 and 2012 net income tripled, it is clear that the
stock is being looked at with extreme skepticism by the market.
There are a number of reasons:
Management change
Mr. Shlomo Yannay, Teva's former CEO, has been replaced by
Jeremy Levin. The latter is an extremely experienced executive, but
has refused to confirm his predecessor's guidance pending a
thorough strategic review that will be made public in mid December.
The market is clearly uneasy for what it perceives as uncertainty
and lack of clarity. We believe there will be no big surprises, but
following our "investigative" activity we believe the new strategy
will focus on the following points, which we think make sense:
Developing its existing pipeline
Divesting non-core businesses
Rationalizing and centralizing R&D, with focus on CNS
Avoiding larger M&A in favor of smaller transactions
Focusing on biologics and emerging markets
Changes in the generics industry
The generics industry is going through a period of transition.
Volume growth continues to be attractive (high single digit), but a
number of adverse changes means that past levels of profitability
are unlikely to be maintained for the following reasons:
First-to-file (and its 180-day exclusivity period) are becoming
rarer, mostly due to…
…authorized generics becoming more frequent
Competition ahead from low cost producers in emerging
countries
European economic downturn
Therefore, we believe that generics sales will continue to grow,
but there will be some pricing and margin pressure at some point.
The trend could be reversed with the arrival of biosimilars, but
the exact timing is uncertain.
Teva experienced some problems in its production facilities in
California and Jerusalem, causing a temporary shutdown and
consequent decrease in production and sales. According to Teva's
management, those issues have been resolved.
Uncertainty about Teva's Copaxone franchise probably lies at the
core of the stock's recent underperformance.
Teva's brand leader is currently the top selling drug for the
treatment of multiple sclerosis, with 2011 sales of $3,570 billion
or 20% of Teva's sales. This remunerative franchise is threatened
by a number of elements:
Immediate generic threat due to patent challenges
Medium-term generic threat following patent expiration in
2015
Immediate threat from recently-launched competing branded
drugs
Because Copaxone clearly represents such a significant share of
Teva's revenue and profit, it is important to quantify the
magnitude of these threats and its impact on the bottom line.
1) Immediate generic threat due to patent challenges:
This threat is no longer relevant. For several years now, Teva
has engaged in a legal battle against Sandoz, which tried to
circumvent Teva's patents challenging their validity. The issue has
been definitively resolved in court with a clear victory for Teva:
no generic version of Copaxone will be authorized before 2015.
2) Medium-term generic threat following patent expiration in
2015.
In 2015, Teva's Copaxone patent will indeed expire. However, it
is not yet clear whether this would lead immediately to a generic
version. It turns out that, due to the very specific chemical
properties of this molecule, any generic version might well need
separate clinical trials before receiving approval, thereby sharply
increasing time-to-market and costs for competitors. This thesis,
repeatedly reiterated by Teva's management, seems to have found
some degree of confirmation by the FDA, according to some of their
past statements.
3) Immediate threat from recently-launched competing branded
drugs
Novartis and Biogen have both recently come up with their own
competing drugs for MS, Gylenia and BG12 respectively, which,
unlike Copaxone, are both oral drugs.
Gylenia has recently been put to market and clinical trials
indicate it is an effective drug, however, there are serious
concerns about its safety profile: Gylenia may impact the heart and
in some cases be fatal. (For details, check out this report.)
4) BG-12 too seems to be very effective and appears to be
initially safer than Gylenia. However, its FDA approval to market
was recently delayed for a further three months.
Copaxone's main disadvantage vis-à-vis its new competitors is
its need to be administered by daily injection. This creates
discomfort for the patient and cosmetic concerns since it may cause
a rash. Gylenia and BG-12 are both oral drugs. While this
difference is indeed important, there are a number of factors that
overwhelmingly suggest that any shift away from Copaxone, while
unavoidable, is likely to be gradual and moderate, rather than
massive and immediate.
Copaxone is currently being approved for a higher dose that can
be administered three times a week, rather than daily.
Copaxone has a very long history of effectiveness and safety.
Its competitors are new to market and only have clinical trials,
which are not error-proof.
Copaxone is a so-called "first line drug". Its competitors, at
least for the moment, are still "second line". That means that
patients receive the drugs of the latter type if, and only if, they
did not respond to any of the first line drugs. This has to do both
with therapeutic history and costs for health insurance
companies.
Most importantly, doctors are extremely reluctant to switch a
stable patient to a new drug. This last point is paramount and has
been hinted at, a few times by Teva's management. We have made our
own inquiries with neurologists in several countries. It turns out
that MS is not just a normal disease, but it is characterized by
acute episodes that may strike at any time.
The patient typically recovers after each episode, but never to
the original level of functioning. In other words, after each acute
episode the patient slides one step further down the disability
scale. It is therefore of paramount importance to keep patients
from experiencing acute episodes. Copaxone reduces the number of
acute episodes experienced by patients. Therefore, it would be a
bad idea to switch a patient away from Copaxone into a new drug
simply because the new drug is oral: if a previously-stable patient
does not respond to the new drug, he might well experience a new
acute episode and slide irreversibly into a lower level of
functioning. Besides, the patient might have adverse reactions to
the new drug. This line of reasoning has been strongly confirmed by
each and every neurologist we have interviewed.
In light of the three arguments above, we believe that Copaxone
is not likely to experience a sharp, sudden decline. It is instead
expected to decline gracefully over the years. We expect the bulk
of the decline to come from pricing pressures, rather than volume
drop.
Copaxone economic impact
Like most other pharma companies, Teva does not disclose the EBITDA
margin of its branded drugs (presumably for competitive reasons).
Our industry interviews however, suggest that the operating margin
on a multi-billion dollar blockbuster like Copaxone should be in
the neighborhood of 70%. In addition to this, the company can
probably save significant amounts of cash reducing marketing
expenses as Copaxone sales begin to ease. Therefore, excluding any
savings in marketing, the complete annihilation of Copaxone sales
could be worth $2.45bn of Ebitda impact.
Valuation
EV/Ebitda Multiples
It may be difficult to assign a precise value to Teva shares at
this moment of uncertainty. However, it would be easy to calculate
a minimum floor for the company's present earnings power, giving
the limited information we have.
We have normalized (excluding cyclicality and one-off items)
Teva's EBITDA at approximately $7.5 billion. Main contributors to
Ebitda are: generics sale, Copaxone, and branded drugs (excluding
Copaxone). We believe that Ebitda from generics should not
materially decrease in the foreseeable future. Any margin drop due
to new competition and decreasing first-to-file should be more than
compensated by gains in volume (industry growing at 8% CAGR) and,
eventually, the introduction of biosimilars.
Likewise, branded drugs (excl. Copaxone) should not decrease
either. There are no upcoming major patent expirations and, on the
contrary, there is a significant pipeline of new drugs about to be
launched.
Therefore, we can safely use TTM normalized Ebitda and subtract
the expected loss from Copaxone. As we saw earlier, Copaxone Ebitda
contribution is roughly $2.5 billion. If we assume that Teva loses
approximately half of that contribution over time, normalized
Ebitda decreases to 6,250.
Teva EV is $47.9 billion so its EV/Ebitda(norm) is equal
to: 7.6X. Teva's close competitors' multiples range from 7.9X to
9.88X and average 8.8X, which suggest an undervaluation of 14%.
Present Earnings Power Calculation
Using our normalized Ebitda, subtracting taxes and maintenance
CAPEX, we reach a net operating profit after tax (NOPAT) of $4.9.
Capitalized at 8%, Teva's operations are worth approximately $61
billion. Subtracting net debt we reach $48.7 billion or $54 per
share, suggesting a 26% margin of safety to current pricing,
according to our analysis..
Of course, the above valuation excludes any growth. It is
likely, however, that Teva will keep growing considerably in the
long term, given its rapidly growing industry and its inherent
competitive advantages (low cost production, patent protection).
Earnings have been growing at 27% CAGR during the last 7 years.
Future growth rates are likely to moderate given Teva's intention
to avoid large acquisitions, Copaxone's slowdown, and generics
uncertainty, but we would expect Teva's earnings to maintain at
least a low double-digit pace for the next 5-10 years.
Risks
We are of the opinion that an investment in Teva at this price
represents a moderate-risk opportunity. Teva operates in a stable
and growing industry, which is relatively insulated by cyclical and
macroeconomic factors. The balance sheet is reasonably strong and
management seems experienced enough.
The biggest risk remains a larger-than-expected drop in Copaxone
sales due to generic and/or branded competition. However, given our
analysis above, we believe that risk to be remote. This is probably
the market's greatest misunderstanding about this company. In
addition to this, the generics industry is also undergoing changes
and the full impact on Teva's income statement is hard to forecast
with precision.
Finally, investors in Teva must be patient, as it might take
time for the market to return valuing Teva at the multiples it
deserves. At this point, there seems to be an adequate margin of
safety to protect investors entering at this level from crippling
losses.
Conclusion
While the overall market is still not overvalued in my opinion,
there are very few deep value opportunities available with an
acceptable risk: this might be one of them.
Disclosure: The author is long Teva stock.
The investments discussed are held in client accounts as of
October 31 , 2012. These investments may or may not be currently
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