Evaluating this case, and seeing how stringent the pharmaceutical industry is, was eye opening experience, especially having had worked on it in a group.
Merck & co., inc. barclays final 3-10-2015Marcel Brussee
What does Merck's $10B buyback plan say about pharma M&A?
Adding $10 billion to its stock buyback program might mean Merck & Co. ($MRK) wants to keep investors happy as its sales continue to shrink. That would be the typical explanation. But The Wall Street Journal sees a different possibility--one the rest of the industry might want to pay attention to.
Source: http://www.fiercepharma.com/story/what-does-mercks-10b-buyback-plan-say-about-pharma-ma/2015-03-26?utm_campaign=SocialMedia
Merck & co., inc. barclays final 3-10-2015Marcel Brussee
What does Merck's $10B buyback plan say about pharma M&A?
Adding $10 billion to its stock buyback program might mean Merck & Co. ($MRK) wants to keep investors happy as its sales continue to shrink. That would be the typical explanation. But The Wall Street Journal sees a different possibility--one the rest of the industry might want to pay attention to.
Source: http://www.fiercepharma.com/story/what-does-mercks-10b-buyback-plan-say-about-pharma-ma/2015-03-26?utm_campaign=SocialMedia
A provider of contract pharma services in high potent manufacturing, Alkermes Contract Pharma Services, outlines here some of the elements that should be considered by a Sponsor/Donor Pharmaceutical company when outsourcing secondary processing (i.e. dosage form transfer, scale-up and commercial manufacture) of a highly potent product.
Application of Technology Acquisition for Corporate GrowthNile University
Technology acquisition is one of the strategies that may be adopted by firms to empower their market footprint and considered as a quick solution to adding competitive advantages to their profile.
Meanwhile, internal R&D attention is essential for market domination and growth.
How does the licensing process differ for in-licensing and out-licensing comp...daisyrmuzzio
PHARMA & BIOTECH LICENSING & PARTNERING:
Filling the Pipeline & Growing Market Share Through Strategic Deal-Making-- March 2-3- San Diego California
Technology is disrupting the process behind drug development. Growing realization that current clinical trial strategies are not sustainable or feasible means one thing - change. But, where do pharmaceutical companies go from here? An integrated clinical trial ecosystem will arise through leveraging emerging business technologies. But, are companies prepared to take advantage?
The Innovation Gap in Pharmaceutical Drug Discovery and New Models for R&D Su...Michael Hu
Whitepaper exploring the root causes behind Pharma Industry's widening Innovation Gap and discusses several R&D innovation models for addressing the productivity conundrum.
This paper aims to study various strategies adopted by pharmaceutical companies to boost innovation. These strategies are usually overlapping and must not be viewed as watertight initiatives.
The penetration of the aforesaid strategies may differ with each pharma. However, on a superficial level it is safe to say that pharmas will largely look outside its own company for drug innovation and early development requirements. This trend will also be enhanced by the fact that most of the late stage drug candidates have already been licensed, and hence the focus will shift to an early stage. The success of these strategies will depend on how many potential drugs will be approved after clinical trials for commercialization.
A provider of contract pharma services in high potent manufacturing, Alkermes Contract Pharma Services, outlines here some of the elements that should be considered by a Sponsor/Donor Pharmaceutical company when outsourcing secondary processing (i.e. dosage form transfer, scale-up and commercial manufacture) of a highly potent product.
Application of Technology Acquisition for Corporate GrowthNile University
Technology acquisition is one of the strategies that may be adopted by firms to empower their market footprint and considered as a quick solution to adding competitive advantages to their profile.
Meanwhile, internal R&D attention is essential for market domination and growth.
How does the licensing process differ for in-licensing and out-licensing comp...daisyrmuzzio
PHARMA & BIOTECH LICENSING & PARTNERING:
Filling the Pipeline & Growing Market Share Through Strategic Deal-Making-- March 2-3- San Diego California
Technology is disrupting the process behind drug development. Growing realization that current clinical trial strategies are not sustainable or feasible means one thing - change. But, where do pharmaceutical companies go from here? An integrated clinical trial ecosystem will arise through leveraging emerging business technologies. But, are companies prepared to take advantage?
The Innovation Gap in Pharmaceutical Drug Discovery and New Models for R&D Su...Michael Hu
Whitepaper exploring the root causes behind Pharma Industry's widening Innovation Gap and discusses several R&D innovation models for addressing the productivity conundrum.
This paper aims to study various strategies adopted by pharmaceutical companies to boost innovation. These strategies are usually overlapping and must not be viewed as watertight initiatives.
The penetration of the aforesaid strategies may differ with each pharma. However, on a superficial level it is safe to say that pharmas will largely look outside its own company for drug innovation and early development requirements. This trend will also be enhanced by the fact that most of the late stage drug candidates have already been licensed, and hence the focus will shift to an early stage. The success of these strategies will depend on how many potential drugs will be approved after clinical trials for commercialization.
Fledgling pharma companies are forging alliances with big pharma companies to develop symbiotic relationships and monetize patents for a win-win. Is this a new age of pharmaceutical innovation? Find out.
Fledgling pharma companies are forging alliances with big pharma companies to develop symbiotic relationships and monetize patents for a win-win. Is this a new age of pharmaceutical innovation? Find out.
12Week 6 Assignment 2In this essay I will discuss my.docxjesusamckone
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Week 6 Assignment 2
In this essay I will discuss my opinion of General Mills greatest strengths and weaknesses. I will choose a way of strategy that the corporation should take to maximize their strengths along with explaining the steps they should take. Two segments of the general environment that has a high influence within the company will be addressed on how it affects General Mills. This essay will also evaluate two forces of competition that is important to General Mills. You will see my evaluation of the greatest external threats and greatest opportunity and explain how they should address them as well.
General Environment
The political environment is significant to the operations of general mills. New regulations regulating food quality standards is a significant threat to company operations. The high standards required for food products by the USA regulations may lead to the company dropping some of its brands which cannot meet the desired standards. Other political issues include changes in tax policies that may lead to higher taxes and reduction in the company’s operating profits. Such regulations can lead to the closure of firms in the industry as many cannot meet high standards and generate enough profits to offset high taxes at the same time.
The economic environment in which the company operates is characterized by rapid changes majorly on the consumer’s incomes which destabilizes their purchasing power hence the company sales. Inflationary trends in the USA are a cause for worry as they lead to rising input prices that often increase the firms operating costs (Green, 2017. The higher interest rates on borrowed capital also increase the company’s operating expenses hence adversely affecting the firm’s cash flows. This is also the case for other firms in the industry as adverse economic situations lead to low sales, high operation cots and small profits to the firms with some tending to operate on losses.
Five Forces of Competition
Item 1
One significant force of completion threatening the general mill's success and continued existence in the industry is the new entrants into the food industry. There are new upcoming industries interested in food processing which often comes with new brands into the market. The new firm's brands threaten the already existing products in the market as they may have a new feature which may lead to general mills losing customers and a significant market share to the new firms. Existence of many substitutes in the market is a considerable threat to the company (Hill, Schilling, & Jones, 2016). Customers often shift to various alternatives in case there is inflation is selling prices of general mills products. It is, therefore, right to argue that the selling prices of general mills products are dictated by the forces of demand and supply. Firms which set lower prices for their products often threaten the general mill's sales as they compete for customers forcing general mills to operate.
The IOSR Journal of Pharmacy (IOSRPHR) is an open access online & offline peer reviewed international journal, which publishes innovative research papers, reviews, mini-reviews, short communications and notes dealing with Pharmaceutical Sciences( Pharmaceutical Technology, Pharmaceutics, Biopharmaceutics, Pharmacokinetics, Pharmaceutical/Medicinal Chemistry, Computational Chemistry and Molecular Drug Design, Pharmacognosy & Phytochemistry, Pharmacology, Pharmaceutical Analysis, Pharmacy Practice, Clinical and Hospital Pharmacy, Cell Biology, Genomics and Proteomics, Pharmacogenomics, Bioinformatics and Biotechnology of Pharmaceutical Interest........more details on Aim & Scope).
All manuscripts are subject to rapid peer review. Those of high quality (not previously published and not under consideration for publication in another journal) will be published without delay.
As part of a class focus on the business side of architecture, me and three other teammates got to research, select, and role play as active members of the DIMELLA SHAFFER company, and present our RFP response.
In this project we used the concepts we had learned throughout the quarter, and developed a creative (video advertisement) in addition to the paper, which was fun.
We designed a model that would take input of a person's specifications, and then based on that would give a meal plan for the person for a week; great for busy people to stay healthy as well.
Read| The latest issue of The Challenger is here! We are thrilled to announce that our school paper has qualified for the NATIONAL SCHOOLS PRESS CONFERENCE (NSPC) 2024. Thank you for your unwavering support and trust. Dive into the stories that made us stand out!
Synthetic Fiber Construction in lab .pptxPavel ( NSTU)
Synthetic fiber production is a fascinating and complex field that blends chemistry, engineering, and environmental science. By understanding these aspects, students can gain a comprehensive view of synthetic fiber production, its impact on society and the environment, and the potential for future innovations. Synthetic fibers play a crucial role in modern society, impacting various aspects of daily life, industry, and the environment. ynthetic fibers are integral to modern life, offering a range of benefits from cost-effectiveness and versatility to innovative applications and performance characteristics. While they pose environmental challenges, ongoing research and development aim to create more sustainable and eco-friendly alternatives. Understanding the importance of synthetic fibers helps in appreciating their role in the economy, industry, and daily life, while also emphasizing the need for sustainable practices and innovation.
Model Attribute Check Company Auto PropertyCeline George
In Odoo, the multi-company feature allows you to manage multiple companies within a single Odoo database instance. Each company can have its own configurations while still sharing common resources such as products, customers, and suppliers.
Palestine last event orientationfvgnh .pptxRaedMohamed3
An EFL lesson about the current events in Palestine. It is intended to be for intermediate students who wish to increase their listening skills through a short lesson in power point.
Unit 8 - Information and Communication Technology (Paper I).pdfThiyagu K
This slides describes the basic concepts of ICT, basics of Email, Emerging Technology and Digital Initiatives in Education. This presentations aligns with the UGC Paper I syllabus.
June 3, 2024 Anti-Semitism Letter Sent to MIT President Kornbluth and MIT Cor...Levi Shapiro
Letter from the Congress of the United States regarding Anti-Semitism sent June 3rd to MIT President Sally Kornbluth, MIT Corp Chair, Mark Gorenberg
Dear Dr. Kornbluth and Mr. Gorenberg,
The US House of Representatives is deeply concerned by ongoing and pervasive acts of antisemitic
harassment and intimidation at the Massachusetts Institute of Technology (MIT). Failing to act decisively to ensure a safe learning environment for all students would be a grave dereliction of your responsibilities as President of MIT and Chair of the MIT Corporation.
This Congress will not stand idly by and allow an environment hostile to Jewish students to persist. The House believes that your institution is in violation of Title VI of the Civil Rights Act, and the inability or
unwillingness to rectify this violation through action requires accountability.
Postsecondary education is a unique opportunity for students to learn and have their ideas and beliefs challenged. However, universities receiving hundreds of millions of federal funds annually have denied
students that opportunity and have been hijacked to become venues for the promotion of terrorism, antisemitic harassment and intimidation, unlawful encampments, and in some cases, assaults and riots.
The House of Representatives will not countenance the use of federal funds to indoctrinate students into hateful, antisemitic, anti-American supporters of terrorism. Investigations into campus antisemitism by the Committee on Education and the Workforce and the Committee on Ways and Means have been expanded into a Congress-wide probe across all relevant jurisdictions to address this national crisis. The undersigned Committees will conduct oversight into the use of federal funds at MIT and its learning environment under authorities granted to each Committee.
• The Committee on Education and the Workforce has been investigating your institution since December 7, 2023. The Committee has broad jurisdiction over postsecondary education, including its compliance with Title VI of the Civil Rights Act, campus safety concerns over disruptions to the learning environment, and the awarding of federal student aid under the Higher Education Act.
• The Committee on Oversight and Accountability is investigating the sources of funding and other support flowing to groups espousing pro-Hamas propaganda and engaged in antisemitic harassment and intimidation of students. The Committee on Oversight and Accountability is the principal oversight committee of the US House of Representatives and has broad authority to investigate “any matter” at “any time” under House Rule X.
• The Committee on Ways and Means has been investigating several universities since November 15, 2023, when the Committee held a hearing entitled From Ivory Towers to Dark Corners: Investigating the Nexus Between Antisemitism, Tax-Exempt Universities, and Terror Financing. The Committee followed the hearing with letters to those institutions on January 10, 202
Acetabularia Information For Class 9 .docxvaibhavrinwa19
Acetabularia acetabulum is a single-celled green alga that in its vegetative state is morphologically differentiated into a basal rhizoid and an axially elongated stalk, which bears whorls of branching hairs. The single diploid nucleus resides in the rhizoid.
Welcome to TechSoup New Member Orientation and Q&A (May 2024).pdfTechSoup
In this webinar you will learn how your organization can access TechSoup's wide variety of product discount and donation programs. From hardware to software, we'll give you a tour of the tools available to help your nonprofit with productivity, collaboration, financial management, donor tracking, security, and more.
Welcome to TechSoup New Member Orientation and Q&A (May 2024).pdf
Elly Lilly, a Pharmecuetical company, group case analysis
1. TEAM CASE
Professor Christopher Myers
MGMT 201
Group members: Pedram Keyvani; Michael Martinez; Tilda Yildirim; Harsh Bhathal; Vraj
Vyas; Peniel Onyukwu
Eli Lilly and Company: Drug Development Strategy(A)
Eli Lilly, a leading pharmaceutical company specializing in treatment of diseases like
depression, diabetes, infections, osteoporosis among others, has a main issue expiring of key
patent, Prozac, an anti-depression drug, which on some aspects could be because of the
controlled operating structure that did not allow room for failure. In a highly competitive and
constantly changing market, it has become a major challenge for the leading pharmaceutical
companies to manage their development costs and generate profitable returns, while funding for
their R&D departments in order to develop new drugs, which is an important part of staying in
business for these types of companies.
Certain critical changes have been taking place in the pharmaceutical industry that have
increased competition and narrowed room for revenue stream. Some of these included,
encouragement of generic prescriptions, enablement of bulk discount rate, and price controls.
These changes forced the pharmaceutical manufacturers to reduce the price of their drugs.
However, the cost of developing a new drug has been increasing drastically since the 1980’s
and 1990’s, as a result of the increased time required to conduct the pre-clinical trials per new
drug application.
All these facts have led to reduced profits, increased costs, higher risks, and increased
competition for the pharmaceutical firms. As a result, Eli Lilly knew that improvements had to
be made in its abilities to develop and introduce new drugs both efficiently and effectively.
Hence, pondering on the best strategy to launch the new Migraine drug they have been
developing. Among the three proposed options, despite having a higher standard deviation,
higher risk, and minimal increased chances in passing clinical trials (as shown in Exhibit 10),
we would recommend Eli Lilly to wait and spend some more time working on the drug to
ensure that the drug successfully passes through its clinicals and is brought into the market.
Scenario 2 must be incorporated to have less time delay (compared to Scenario 3) and finish the
2. process in time before Prozac Patent finishes in 2003 (Exhibit 11) to ensure that the drug
successfully passes through its clinicals and is brought into the market.
In our process on deciding which of the three options is most suitable we evaluated the
pros and cons (tradeoffs) for each; either take the lead migraine compound directly into clinicals
and bring it to market as quickly as possible, Spend more time to refine the current lead migraine
compound [using combinatorial chemistry], or go back to basic research and spend significantly
more time to search for a new migraine drug platform [using combinatorial chemistry]. The
choice between each course of action came down to three baseline issues: Time to market,
Diversity of leads, and Method of chemistry used. Each choice would mean sacrificing focus on
different aspects of the key issues.
If we were to opt for the first course of action — Take the lead migraine compound
directly into clinical and bring it to market as quickly as possible — Lilly would reduce risk of
revenue loss associated with additional months delay as well as losses to opportunity cost
associated with allowing additional time for competitors to take advantage of the market. In a
highly competitive market, every additional month increases risk exponentially. To a different
tone, taking the compound directly to trials runs a higher risk of not passing. While there is
potential to save time and increase revenue, pushing a compound through too quickly in its
development cycle could result in the product failing before it makes it to market. This option
also eliminates the possibility to find alternative leads that may be more successful in clinical
trials than the existing compound.
If we were to opt for the second course of action — Spend more time to refine the current
lead migraine compound [using combinatorial chemistry] — Lilly increases risk of revenue loss
and competitor entry to the market. With Lilly’s team of experts assuming an additional
development time of about nine months, we would run a sizable risk of competitor consolidation
and market entry which could hinder our potential earnings. However, allowing more time to
refine the compound would decrease risk of failure in resource intensive clinical trials, and
increase chance to move product to market. Additionally, using the emerging technology,
combinatorial chemistry, as the refinement and research method would further its own
development and contribute to Lilly’s ability to deploy the technology throughout its business.
As the method has the opportunity to shave significant time off of the development cycle, this
could give Lilly a significant competitive edge down the road.
3. Lastly, if we were to opt for the third course of action — Go back to basic research and
spend significantly more time to search for a new migraine drug platform [using combinatorial
chemistry] — we would see a significant increase in the probability that we find a compound that
is successful in clinical trials and makes it to market. With clinical trials having such a low
likelihood of successful performance, the more time a company spends on development,
diversifying leads and patent opportunity, the better off the compound and competitive edge will
be. Additionally, the added development time will also lead to more time spent working with the
combinatorial chemistry method, furthering Lilly’s ability to use it on a greater scale. On the flip
side, the added months of research could lead to a large loss in revenue and allow significant
time for competitors to take advantage of the market with similar products. This risk could push
Lilly out of the market completely.
All of the trade offs considered, we decided to go with the second course of action: to
spend more time to refine the current lead migraine compound, using combinatorial chemistry.
We encourage Eli Lilly to maintain in developing the platform they formed already instead of
searching for a new platform due to various reasons.
Firstly, as seen in Exhibit 1, the Central Nervous System market share was projected to
increase by 63% in 2000 amounting to $13.1 billion. If this estimate is correct, it indicates that
there is real value in exploring to confirm the correct method for developing the drug to tackle
migraines. This will improve Eli Lilly’s chances of taking over this new market. Also drug
development process is a long and highly costly process to deal with. As stated in the Exhibit 2,
pharmaceutical companies spend approximately $230 million and 14.8 years on developing a
new compound for a single drug.If Eli Lilly decides to invest in another drug making process
they would acknowledge to spend millions and years on an idea that doesn’t exist. Instead of
doing this, spending that time and money on something they already have will be more profitable
in long term.
One drawback they might face would be in terms of money. Although spending more
would mean that the company would lose money and may have to pay out-of-pocket, it would
be in their benefit if Eli Lilly waited for a little bit longer and continued to refine the migraine
compound they already have. A company does not need to always reinvent the wheel, but
instead refine the wheel. Renovating the migraine compound could take out chances of
possible flaws/error, and continue time in research/development. This would save the company
4. time and resources when they release the product to market. In the current time period, it is
difficult to reach the number one position if one was not the first to release it. However, as an
established pharmaceutical company, the chances are better. Taking Apple as an example, we
can approach the same problem from the technology industry. Apple was not the first to
market in the smartwatch category, in fact it was one of the later contenders, coming out three
years after some of the first big smartwatches came out. Today, Apple dominates the
smartwatch category by a whopping 59% in the cellular connectivity category. Additionally,
the Apple Watch was the 4th best selling gadget of 2017. We can take this information from
the technology industry and position it for the pharmaceutical industry. At the end of the day,
it is the consumer market, where most industries have similar consumer logic.
All in all, after considering the progress that has been made thus far, using combinatorial
chemistry, we believe that a few additional months of development will best position Eli Lilly to
introduce a successful compound to clinical trials, further develop the emerging technology, and
handle marginal risk associated with added time.