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Same-Day Analysis

What Would a Schering-Plough/BMS Merger Look Like?

Published: 19 September 2006
In light of recent rumours over a potential merger between U.S. drug firms Schering-Plough and Bristol-Myers Squibb (BMS), Global Insight takes this opportunity to examine what such a deal would look like.

Global Insight Perspective

 

Significance

While the merger may not (and, for a variety of reasons, probably will not) materialise, the potential for such a deal highlights major problems that do not just affect Schering-Plough and BMS, while revealing that there is still significant room for restructuring in the global pharmaceutical industry.

Implications

A merger would shepherd Schering-Plough straight into uncharted territory among the top five of Big Pharma, but—more importantly—it would fill gaping holes in the company's pipeline. BMS’s problems are more pressing, and Schering-Plough’s portfolio of growth-drivers would provide significant short-term relief, while cost-cutting would build its financial capacity.

Outlook

Global Insight remains guarded on the prospects for a Schering-Plough/BMS merger; we believe that BMS will wait for a better offer, which lacks the added complexities of Schering-Plough’s network of joint ventures (JVs). We also believe that the likelihood of such an offer being made soon is very high.

SchePloBMS?

As reported yesterday by Global Insight, New Jersey-based newspaper the Star Ledger is claiming that Schering-Plough is taking “serious” steps towards making a bid for fellow U.S. drug-maker Bristol-Myers Squibb (BMS). Speculation is rife in the global pharmaceutical industry over what this may mean for the market, although it is important to stress that BMS and Schering-Plough have neither commented on the Star Ledger report nor offered any general comment on merger negotiations (the newspaper itself notes that Schering-Plough has “yet to approach” BMS with a formal proposal). As a result, Global Insight is taking this opportunity to analyse the overall likelihood of a merger (which we consider small), while taking a look at what the speculation already says about an industry struggling under the weight of red tape and generic assaults.

The rumours stem from the early admittance, following the departure of CEO Peter Dolan, that BMS will consider any and all offers of a merger or takeover. The board is clearly looking to build shareholder value, after the company took a severe beating over its stumbled defence of the patent for blockbuster stroke drug Plavix (clopidogrel). At the opposite end, Schering-Plough has spent most of the last three years getting itself out of a conundrum not entirely dissimilar to that which BMS currently faces. An entirely new management team was put in place in 2003, largely consisting of former Pharmacia & Upjohn/Pharmacia Corporation officials who left after the takeover by Pfizer (U.S.). New CEO Fred Hassan immediately put in place a slow-burning turnaround strategy, centring on building critical mass and portfolio strength, partially at the expense of a promising pipeline.

Two major outcomes of this strategy included the joint ventures (JVs) with Johnson & Johnson (J&J, U.S.), relating to Remicade (infliximab) and Phase III follow-up candidate golimumab, and Merck & Co (U.S.), which involves cholesterol drugs Vytorin (ezetimibe/simvastatin) and Zetia (ezetimibe). It is these two partnerships that form the main impediments to a potential merger with BMS—or at least complicate matters significantly. In order to maintain these JVs without J&J or Merck purchasing Schering-Plough’s stake, Hassan’s company would need to maintain at least 40% control (according to the Merck agreement) or 50% (according to the J&J agreement) of the new company. This would put major pressure on the finances of a company that is considerably smaller than BMS. While Schering-Plough has built a strong cash flow to support such an initiative, it is clear that substantive debt would need to be created to finance a merger; however, it is important to remember the low overall levels of debt in the global pharmaceutical industry, and the risk-averse nature of shareholders who are already looking at the vagaries of pipeline development.

The Star Ledger commented that a complicated stock-for-stock “reverse merger” might be instigated, in order to maintain Schering-Plough's JVs. However, this would mean that BMS was paying a significant premium for Schering-Plough’s share, defying the basic point of a merger for BMS—the creation of shareholder value. Herein lies the major problem that we consider to be the major impediment to the merger. Therapeutically, there aren’t many problems, with Schering-Plough and BMS forming a fairly nice fit; Vytorin and Zetia provide a nice fold for Pravachol (pravastatin) and Plavix (clopidogrel) on the cardiovascular side, while BMS’s new drugs, particularly in the field of oncology, would reduce Schering-Plough’s reliance on the Merck JV and fit nicely with the Temodar (temozolimide) franchise. They also hold complementary focus on HIV/AIDS research. In terms of geographic reach, we do not believe that this would be a top-heavy company in the United States, given Schering-Plough’s relatively small presence there (US$2.4 billion in 2005, or 31% of net sales, compared to US$8.1 billion/70% of net sales at BMS).

BMS and Schering-Plough: Combined Portfolio

Brand

API*

Company

Indication

2005 Sales (US$ mil.)

% Change, Y/Y

Plavix

Clopidogrel

BMS

Atherosclerosis

3,823

14.9

Pravachol

Pravastatin sodium

BMS

Cholesterol

2,256

-14.4

Avapro / Avalide

Irbesartan

BMS

Hypertension

982

5.6

Remicade

Infliximab

Schering-Plough

Arthritis

942

26.3

Abilify

Aripiprazole

BMS

Schizophrenia, Bipolar

912

53.8

PEG-Intron

Peginterferon alfa-2b

Schering-Plough

Hepatitis

751

33.4

Taxol

Paclitaxel

BMS

Breast cancer, NSCLC, Ovarian Cancer

747

-24.6

Nasonex

Mometasone furoate monohydrate

Schering-Plough

Allergy, Rhinitis

737

24.1

Sustiva

Efavirenz

BMS

HIV/AIDS

680

9.5

Clarinex/Aerius

Desloratidine

Schering-Plough

Allergy, Rhinitis

646

-6.6

Temodal / Temodar

Temozolomide

Schering-Plough

Brain cancer

588

28.1

Erbitux

Cetuximab

BMS

Colorectal cancer, Head & Neck Cancer

413

58.2

Claritin

Loratidine

Schering-Plough

Rhinitis

371

15.6

Cipro

Ciprofloxacin

Schering-Plough

Antibiotics

146

239.5

Zerit

Stavudine

BMS

HIV/AIDS

216

-20.6

* API: Active pharmaceutical ingredient

Outlook and Implications

The creation of synergies between the two companies would provide significant upside for the immediate prospects of the combined company; such cost reductions and cash creation usually amount to 11-15% in the drug industry. Based on 2005 sales, it would create a company with revenue of US$28.7 billion and an operating income of US$5.4 billion (Schering-Plough’s margins continue to be very poor, although they are improving slowly). Maximising efficiency in the R&D department would clearly play a critical role, with Schering-Plough maintaining a relatively high rate of R&D spending as a share of revenue, at nearly 20%; BMS's rate of 14.3% is more in line with the industry standard (Schering-Plough’s high R&D expenditure and selling, general and administrative (SGA) cost ratio are the main factors behind its depressed margins). The combined R&D budget would stand at US$4.6 billion—one of the largest in the industry—and would oversee a highly competitive pipeline.

The Schering-Plough/BMS speculation tells a story of unrest in the global pharmaceutical industry—both within companies themselves and among shareholders and analysts. For a long time, there has been widespread dissatisfaction with the manner in which some of Big Pharma’s former bright stars are performing. The fact that some of the old guard in pharma management at Pfizer, Merck and BMS have left within the space of a year reflects this dissatisfaction, and the acquisition of Schering-Plough’s management team would clearly form a critical part of BMS’s thinking if merger proceedings go ahead. The ascension of relatively unexpected leaders such as lawyer Jeff Kindler at Pfizer and manufacturing strategist Dick Clark at Merck shows that Big Pharma is looking for new ideas, in new ways.

However, we do not consider that the merger currently makes strategic sense; the leverage that Schering-Plough would need to finance the initiative would lay waste to several years of highly successful turnaround, while a reverse merger simply does not pay dividends for BMS. The uncertainties of Plavix litigation, as well as Schering-Plough’s JVs, provide other downsides. Instead, while companies such as Novartis (Switzerland) have quickly distanced themselves from interest in BMS, we consider such players as AstraZeneca (U.K.) and Sanofi-Aventis (France) to be more attractive propositions, unburdened by some of the risk factors that Schering-Plough carries. Watch this space.

BMS and Schering-Plough: Late-Stage Pipeline

Company

Brand

API

Indication

Status

Comments

Schering-Plough

 

Garenoxacin

Antibiotics

Filed

Licensed from Toyama;Astellas holds Japanese rights; filed in March 2006 in U.S.; clashes with Avelox

Schering-Plough

Remicade

Infliximab

IBD

Filed

 

Schering-Plough

Zetia

Ezetimibe

Cholesterol

Filed

Co-developed/marketed with Merck; Marketed in Japan by Bayer

Schering-Plough

Noxafil

Posaconazole

Anti-fungals

Filed

U.S./EU

Schering-Plough

Noxafil

Posaconazole

Anti-fungals

Filed

U.S.

Schering-Plough

Temodal / Temodar

Temozolomide

Brain cancer

Filed

Japan

Schering-Plough

Zetia

Ezetimibe

Cholesterol

Filed

Japan

BMS

Pargluva

Muraglitazar

Diabetes

Filed

Co-development with Merck; approvable; development and agreement terminated

BMS

Sprycel

Dasatinib

Leukaemia

Filed

Approved

Schering-Plough

Integrilin

Eptifibatide

ACS

Phase III

Marketing rights from Millennium Pharmaceuticals

Schering-Plough

Nasonex

Mometasone furoate monohydrate

Allergy, rhinitis

Phase III

 

Schering-Plough

Peg-Intron

Peginterferon alfa-2b

Melanoma

Phase III

 

Schering-Plough

Asmanex

Mometasone furoate

Asthma

Phase III

Japan

Schering-Plough

 

Loratidine / montekulast

Rhinitis

Phase III

JV with Merck; combination of Claritin and Singulair

Schering-Plough

Remicade

Infliximab

IBD, arthritis

Phase III

 

Schering-Plough

Sarasar (SCH-663366)

Lonafarnib

Myelodysplastic syndrome

Phase III

 

Schering-Plough

Suboxone / Subutex

Buprenorphine

Addiction (smoking, alcohol, opiates)

Phase III

US marketing rights are with Reckitt Benckiser

Schering-Plough

Temodal / Temodar

Temozolomide

Melanoma

Phase III

 

Schering-Plough

Vytorin

Simvastatin/ezetimibe

Cholesterol, ACS, renal disease

Phase III

Joint Venture with Merck

Bristol-Myers Squibb (BMS)

 

Edifoligide

Transplant

Phase III

Co-development with Corgentech; failed to meet primary endpoints in March 2005, BMS terminated agreement

BMS

MDX-010

Ipilmumab

Melanoma

Phase III

Co-development with Medarex

BMS

 

Ixabepilone

Breast cancer

Phase III

Studied as monotherapy and with capecitabine combination

BMS

Javlor

Vinflunine

Bladder cancer, NSCLC

Phase III

Co-development with Pierre Fabre Excluding Europe

BMS

 

Saxagliptin

Diabetes

Phase III

DPP-IV inhibitor

BMS

LEA-29Y

Belatacept

Transplant

Phase III

 

Schering-Plough

 

Vicriviroc

HIV/AIDS

Phase II

Co-development with ViroLogic

Schering-Plough

PDE-5 Inhibitor

 

Sexual/erectile dysfunction

Phase II

 

Schering-Plough

Sarasar (SCH-663366)

Lonafarnib

Breast cancer, unspecified

Phase II

 

Schering-Plough

 

Pleconaril

Asthma

Phase II

 

Schering-Plough

Adenosine 2a Receptor Antgaonist

 

Parkinson's

Phase II

 

Schering-Plough

CNTO-148

Golimumab

Arthritis

Phase II

in-licensed from Centocor

Schering-Plough

Thrombin receptor antagonist

 

Thrombosis

Phase II

 

Schering-Plough

SCH-503034

 

Hepatitis

Phase II

 

Schering-Plough

 

Mometasone / formoterol

Asthma

Phase II

Joint development with Novartis; combination of Singulair and Foradil

Schering-Plough

Temodal / Temodar

Temozolomide

Brain cancer, unspecified solid tumours

Phase II

 

BMS

Javlor

Vinflunine

Breast/ovarian cancer

Phase II

Co-development with Pierre Fabre Excluding Europe

BMS

 

Razaxaban

Thrombosis

Phase II

 

BMS

DPC-083

 

HIV/AIDS

Phase II

 

BMS

BMS-214662

 

Unspecified

Phase II

Nonthiol farnesyl transferase inhibitor

BMS

CRF1 antagonist

 

Depression

Phase II

 

BMS

Attach Inhibitor

 

HIV/AIDS

Phase II

 

BMS

LFA-1 Antagonist

 

Psoriasis

Phase II

 

Source: Companies/Global Insight

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