From Breakthrough to Blockbuster

From Breakthrough to Blockbuster
Author: Donald L. Drakeman
Publisher: Oxford University Press
Total Pages: 241
Release: 2022-02-14
Genre: Science
ISBN: 0197626300

Financial Times Business Top Title March 2022 How could a large collection of small companies, most with fewer than 50 employees, rise to compete with Big Pharma, one of the world's most breathtakingly expensive and highly regulated industries? Beginning in the 1970s, several scientific breakthroughs promised to transform the creation of new medicines. As investors sought to capitalize on these Nobel Prize-winning discoveries, the biotech industry grew to thousands of small companies around the world. Each sought to emulate what the major pharmaceutical companies had been doing for a century or more, but without the advantages of scale, scope, experience, and massive resources. Biotech companies have met the challenge by creating nearly 40% more of the most important treatments for previously unmet medical needs. Moreover, they have done so with much lower overall costs. From Breakthrough to Blockbuster: The Business of Biotechnology focuses on both the companies themselves and the broader biotech ecosystem that supports them. It paints a portrait of the crucial roles played by academic research, venture capital, contract research organizations, the capital markets, and pharmaceutical companies, demonstrating how a supportive environment enabled the entrepreneurial biotech industry to create novel medicines with unprecedented efficiency. In doing so, it also offers insights for any industry seeking to innovate in uncertain and ambiguous conditions.

Economics and Management in the Biopharmaceutical Industry in the USA

Economics and Management in the Biopharmaceutical Industry in the USA
Author: Rachel Kim
Publisher: Routledge
Total Pages: 212
Release: 2018-12-07
Genre: Business & Economics
ISBN: 135101269X

From a managerial perspective, the biopharmaceutical industry represents a competitive, fast-changing, intellectually-powered, innovation-driven sector. Many management scholars have studied this discontinuous era to make sense of strategic behavior and the cognition of firms and top managers. A past look at the biopharmaceutical industry provides answers to questions that most managers have. For example, what options do you have and what actions do you take when new firms enter your industry? In the 1970s, new biotechnology firms, funded by venture capitalists, appeared in the pharmaceutical industry with new knowledge. Successful pharmaceutical firms decided to collaborate with the new entrants and forge relationships to develop and create new, biotechnology engineered drugs. Thus, the addition of new biotechnology firms ushered in a new business model based on strategic alliances. Strategic alliances have now become an industrial norm called open innovation. The author looks at the historical path of the biopharmaceutical industry, particularly in the United States. While the pharmaceutical industry’s main contributions to society are substantial, there are pressing challenges the industry must face, such as an increase in infectious disease outbreaks or the global aging population, which require new types of care, additionally, mental health care and prescription painkiller addiction are persistent issues with economic repercussions to both federal and local governments. This book presents a holistic view of the biopharmaceutical industry, putting it in a historical context. It will best serve those who are eager to learn about this dynamic, fast-evolving industry and who would like to tackle current biopharmaceutical industry issues in the United States and be prepared for future industry challenges.

Early-stage Strategic Alliance Formation in the Life Science Industry

Early-stage Strategic Alliance Formation in the Life Science Industry
Author: Vedant Bharat
Publisher:
Total Pages: 204
Release: 2019
Genre: Pharmaceutical industry
ISBN:

The life sciences industry spectrum consists of the big pharmaceutical companies ("big pharma") on one side and small to medium biotech companies (SMEs) on the other. Burdened by a multitude of challenges and the need to mitigate them encouraged the SMEs and big pharma to engage in open innovation activities, such as forming strategic alliances. The success of these alliances depends on the SME and big pharma understanding each other’s business strategies, i.e. the perspectives and drivers that motivate them to form alliances. However, SMEs often develop assets without a complete understanding of what drives big pharma’s interest and therefore, fail to meet their criteria for partner selection and alliance formation. Additionally, the literature highlights a recent trend that big pharma is prioritising their focus on inbound open innovation for assets at early-stages in the drug development pathway. This change in big pharma focus towards early-stage assets and specific criteria used for partner selection forms the basis of this study. A qualitative and explorative case study research design informed by a review of secondary resources, field notes/observations and conducting five semi-structured interviews on senior big pharma managers was done to delve deeper into the research topic of early-stage strategic alliance formation. At early stages of asset development and initial interactions with SMEs, big pharma considers four criteria and their associated sub-criteria; trust (benevolence and competence), complementarity (skill and resources based), commitment (goal alignment) and financial pay-off (IP position, geographic proximity, novelty, competitive differentiation, reimbursement), to determine strategic fit. The interactions/interplay between these criteria was considered throughout the decision-making processes of big pharma (from pre-selection to deeper/full evaluation) by multiple team members. This thesis outlines the factors that influence the initial stages of alliance formation and provides a framework that depicts the interplay between the key SME-related criteria that big pharma consider while forming early-stage strategic alliances. By considering this framework, SMEs can strategize their initial interactions with the big pharma to overcome the barriers to early-stage of alliance formation.

Strategic Alliances in Biotechnology and Pharmaceuticals

Strategic Alliances in Biotechnology and Pharmaceuticals
Author: Hans-Werner Gottinger
Publisher:
Total Pages: 0
Release: 2010
Genre: Alliances stratégiques (Affaires).
ISBN: 9781608769971

This book covers a strategic industry analysis of a globally operating pharmaceutical and biotechnology industry. Both biotechnology and large pharmaceutical firms compete in a network industry characterised by rapid technological change which leads to industry change and market structure. In particular, these firms depend on the creation of new knowledge. New knowledge presents particular issues regarding transferability. Innovation potentials and alliance competencies should be prevalent in any market characterised by fast changing intangible assets , given the difficulties in trading intangibles; moreover, in industries with very high rates of technology change, technologies can be introduced that create new market segments, obsolesce existing product lines, and create substantial competitors from previously little-known firms.

Leading Biotechnology Alliances

Leading Biotechnology Alliances
Author: Alice M. Sapienza
Publisher: Wiley-Liss
Total Pages: 226
Release: 2001-04-09
Genre: Business & Economics
ISBN:

Nearly all pharmaceutical and biotechnology companies are forming strategic alliances, presenting formidable management challenges. "Leading Biotechnology Alliances: Right from the Start" provides immediately applicable tools for managing human relationships involved in these strategic alliances.

Economic Dimensions of Personalized and Precision Medicine

Economic Dimensions of Personalized and Precision Medicine
Author: Ernst R. Berndt
Publisher: University of Chicago Press
Total Pages: 361
Release: 2019-04-22
Genre: Business & Economics
ISBN: 022661123X

Personalized and precision medicine (PPM)—the targeting of therapies according to an individual’s genetic, environmental, or lifestyle characteristics—is becoming an increasingly important approach in health care treatment and prevention. The advancement of PPM is a challenge in traditional clinical, reimbursement, and regulatory landscapes because it is costly to develop and introduces a wide range of scientific, clinical, ethical, and socioeconomic issues. PPM raises a multitude of economic issues, including how information on accurate diagnosis and treatment success will be disseminated and who will bear the cost; changes to physician training to incorporate genetics, probability and statistics, and economic considerations; questions about whether the benefits of PPM will be confined to developed countries or will diffuse to emerging economies with less developed health care systems; the effects of patient heterogeneity on cost-effectiveness analysis; and opportunities for PPM’s growth beyond treatment of acute illness, such as prevention and reversal of chronic conditions. This volume explores the intersection of the scientific, clinical, and economic factors affecting the development of PPM, including its effects on the drug pipeline, on reimbursement of PPM diagnostics and treatments, and on funding of the requisite underlying research; and it examines recent empirical applications of PPM.

Risk-sharing in the Pharmaceutical Industry

Risk-sharing in the Pharmaceutical Industry
Author: Gerrit Reepmeyer
Publisher: Springer Science & Business Media
Total Pages: 306
Release: 2006-02-25
Genre: Business & Economics
ISBN: 379081668X

The productivity in pharmaceutical research and development faces intense pres sure. R&D expenditures of the major US and European companies have topped US$ 33 billion in 2003 compared to around US$ 13 billion just a decade ago. At the same time, the number of new drug approvals has dropped from 53 in 1996 to only 35 in 2003. Moreover, the protraction of clinical trials has significantly reduced the effective time of patent protection. The consequences are devastating. Monopoly profits have started to decline and the average costs per new drug have reached a re cord level of close to US$ 1 billion today. As a result, any failure of a new sub stance in the R&D process can lead to considerable losses, and the risks of introduc ing a new drug to the market have grown tremendously. Particularly if a company is highly dependent on just a handful of mega-selling blockbuster drugs, the risks can be even greater. For example, Pfizer generated about 90% of its worldwide revenues in 2002 with just 8 products. Any shortfall of a promising late-stage drug candidate would have left Pfizer with a gaping hole in its product portfolio. In order to deal with these risks, many pharmaceutical companies have started to organize their R&D in partnership. In fact, more than 600 alliances in pharmaceutical R&D are signed every year.