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RESEARCH CAREERS IN DRUG DISCOVERY & DEVELOPMENT
Dr. Bhaswat S. Chakraborty Sr. VP & Chair, R&D Core
CommitteeCadila Pharmaceuticals Ltd.
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CONTENTS Discovering & Developing New Drugs: Overview Discovery Development Lead Compound to Regulatory Approval Regulatory Approval to Marketing Drug DD Multi-Disciplines Drug DD & Other R&D Scientists Adaptation of a Fresh Graduate in his/her R&D Roles Team playing Finding a Mentor Notes on working in Big Pharma Demystifying Myths Concluding Remarks 2
DISCOVERING & DEVELOPING NEW DRUGS: OVERVIEW
Highly time and cost intensive Three stages: Discovery: Identifying new compounds that
help treat disease Development: Administering the new drug to
animals and humans to make sure it is safe and effective
Manufacturing: Producing the new drug in large quantities for distribution
3
IMPACT OF NEW MEDICINES IN LAST 100 YRS
Human life expectancy has doubled both developed and developing economies
One of the main reasons: better medicines than before In some cases a better QoL Backbone of effective and safe medicines
Research in the areas drug discovery, preclinical, formulation development and clinical studies
However, last two decades have seen very high cost of drug R&D ~couple of billion US dollars
Despite this intimidating expense and the patents-warfare, R&D for good medicines are on
Good medicines are still being discovered and developed4
Chakraborty B.S. (2012) PharmaTech, 3: 22-26
DRUG DISCOVERY Selection and characterization of the target disease
Disease must be well understood and characterized Protein (usually) associated with the disease can be targeted by
a lead compound with desirable properties Which may cure the disease or control it
With HTS robotics, data processing and control softwares, liquid handling devices, and sensitive detectors, a researcher can now conduct millions of chemical, genetic or pharmacological tests in few days
Such in silico molecular modeling is actually a tremendous acceleration of the drug discovery process 40 years to understand the cholesterol biosynthesis pathway to
develop the statin drugs – those that inhibit the enzyme HMG-CoA reductase, the rate limiting step in cholesterol biosynthesis
But 3 yrs for a molecular-level understanding of the role of the HER-2 receptor in breast cancer to develop Herceptin® 6
Chakraborty B.S. (2012) PharmaTech, 3: 22-26
DEVELOPMENT OF THE LEAD COMPOUNDS
Only 3-4 lead compounds emerge per 2000 structures examined Subjected to preclinical efficacy and safety and toxicity testing The first in humans, viz. Phase I studies
Human toxicity, maximum tolerated dose and pharmacokinetics (ADME – absorption, distribution, metabolism and elimination) of the administered drug
Also be a slight hint of human efficacy of the lead drug in some cases If the toxicity profile and tolerability of the drug are acceptable
Tested in limited number of patients first (a Phase II study) finally in a substantial number of patients in epidemiologic setup
(Phase III study) Results from clinical trials are fed back to enhance the next round
of target selection and lead identification and optimization Highest goal of drug DD is that the drug is safe & effective
in its proposed use(s) & benefits outweigh the risks 9
DEVELOPMENT OF THE LEAD COMPOUNDS
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Figure 2: The lead compounds are screened in animals and then select lead compounds, only a few, are taken to the subsequent clinical studies.
Chakraborty B.S. (2012) PharmaTech, 3: 22-26
REGULATORY APPROVAL TO MARKETING At the end of Phase II, the FDA and sponsors try to come to an
agreement on Phase 3 conduct How often the FDA meets with a sponsor varies, but this is one of
two most common meeting points prior to NDA The other most common time is pre-NDA, right before an NDA is
submitted Phase III studies begin if evidence of effectiveness is shown in Phase
II Ph III: more information about safety & effectiveness,
Studying different populations and different dosage Using the drug in combination with other drugs N=Hundreds to about 3,000
Results of Phase III studies provide the main evidence of efficacy and safety in a Regulatory application
Following the Regulatory approval the drug can be marketed in that country
Post-marketing study commitments (Phase IV) are conducted after the FDA has approved a drug for marketing
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Biology ChemistryAssay development Analytical Chemistry
Cellular Biology Medicinal and Synthetic chemistry
Electrophysiology Rational Design
Genomics and molecular biology Computational chemistry
Medicine In silico and de novo design
(Behavioral) pharmacology High-throughput screening
Physiology Related Sciences Protein biochemistry, expression, and synthesis
Engineering
Protein engineering and biopharmaceuticals
Mathematics
Proteomics Statistics
Structural biology and crystallography
Bio and chemi-informatics
Veterinarian siences IT, hardware and software design
Bell M, Science Careers, March 19, 2004
COMMON DRUG DISCOVERY DISCIPLINES
DRUG DD & OTHER R&D SCIENTISTS Most of the pharmaceutical R&D scientists have a post
graduate training from a recognized academic institution in their respective fields
About 10% of these individuals are PhD, MD & MVSc degree holders
Other requirements include high IQ, goal setting, problem solving and team playing skills Can also be gifted with a high EQ or MBA degree (necessary for
management positions)
An eye for details and writing expressly in technical English Inclination for experiments, hypothesis generation Training in research methologies ….
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Chakraborty B.S. (2013) PharmaTech, 4: 18-20
ADAPTATION OF A FRESH GRADUATE IN HIS/HER R&D ROLES R&D scientists are mostly concentrated in private sector
pharma business companies and some academic institutions 400,000 people globally in pharma, biotech and medical devices R&D
Majority get a job orientation following their graduation from academia and only after joining their employment
Formal training in on-going projects and SOPs by the minute stepwise descriptions of processes and rigidity of specifications
The hierarchy of reporting and the reality of owning the responsibilities are also strikingly novel for most of the entry level scientists
Challenge is to be a part of large multidisciplinary drug discovery & development teams
A suitable mentor can hold the hands of a fresh graduate during these bewildering times
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Chakraborty B.S. (2013) PharmaTech, 4: 18-20
DEVELOPMENT OF TEAM PLAYING SKILLS All pharma R&D activities are carried out in “team” set up
these days Teams could be mainly of three types:
Management, operational and expertise Management teams have the roles of leading and co-ordinating Operational teams consist of actual delivery of projects and
problem solving oriented team players Experts give critical input and also provide depth expertise
wherever needed Desirable that there is no artificial competition and
dissatisfaction in one’s mind regarding her role If roles remain unclear, domineering and put-down behaviours
by certain role players become rampant at the cost of others.
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Chakraborty B.S. (2013) PharmaTech, 4: 18-20
FINDING A CAREER MENTOR Mentor in Sanskrit is “Mantradata”
or giver of knowledge E.g, Krishna-Arjuna (ancient),
Gandhi-Neheru, Sir Humphry Davy- Michael Faraday
R&D mentor can inspire and give insight in many career related issues Can explain difficult scientific
concepts, which can lay foundation of the mentee’s understanding and save a great deal of time and energy
Help the young scientist to design a difficult clinical trial or experiment and solve problems
Correct interpretation and scope of new FDA & other Science guidances is another insight that a mentor can give
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Chakraborty B.S. (2013) PharmaTech, 4: 18-20
1. You don’t get to publishNot true. Most pharmaceutical companies strongly encourage publication of
scientific work and often link bonus payments to high publication levels.
2. You don’t get to go to conferences Not true. Pharmaceutical companies generally encourage scientists from all
levels to attend key conferences as both delegates and presenters.
3. You just screen or make compounds all day Not true. A drug discovery operation is made of many different disciplines
and involves many activities including a lot of basic research.
4. You are not free to follow your own interests or to be innovative Not true on both counts. Innovation and creativity is strongly encouraged
and scientists spend significant time exploring new hypotheses and approaches
5. The science is not as good as in academia Not true. Pharmaceutical companies claim many high-profile publications,
patents and groundbreaking concepts every year. Bell M, Science Careers, March 19, 2004
THE FIVE MYTHS OF WORKING FOR INDUSTRY
WHERE TO FIND AN EMPLOYMENT? Large drug manufacturing and biotech companies in PBE Contract research organizations (CROs) Academic institutions Governmental agencies
Regulatory Research Policy
Laboratories developing new drug therapies Universities or hospitals Supervising clinical drug trials Manufacturing centers for large-scale production of
medications Pre-Clinical CROs
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BIG PHARMA & THE PHARMACEUTICAL-BIOTECH ECOSYSTEM (PBE) Big pharma is atop the ecosystem with capital and resources
needed to commercialize new drugs Their goal is to enrich their drug development pipeline,
leveraging their expertise in regulatory submission, reimbursement, and commercialization of product
They are the integrators, orchestrating the drug development process with members of the ecosystem
The ecosystem concept offers a richer context than established supply chain models because the PBE is a dynamic, growing environment
Members can use funding from big pharma to build business that potentially can compete against established companies
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McCarthy R, Science Careers, March 19, 2004
PREPARING FOR A CAREER IN THE PBE First, increase the value of your skills so it can benefit
yourself and your employer Going to graduate school and training in laboratories with
intellectually stimulating environments Sometimes working as a technician in a university research
laboratory can be helpful Second, understand the dynamics of value shifts in the PBE.
Develop an interest in technology management New concepts such as disruptive technology and open innovation are
changing the way established companies are developing new products
Third, engage in dialogue with others who are more experienced than you in this field
And lastly, remain a lifelong student Genomics/proteomics revolution are just beginning Opportunities for technology-astute scientists are abound in future
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McCarthy R, Science Careers, March 19, 2004
YOU MAY SPECIALIZE IN: Designing new drug therapies using natural or synthetic
(man-made) ingredients Discovering new ways to use existing drugs to treat
different types of disease Studying how disease affects the body and what causes
some people to develop certain types of disease Studying how the human body responds to medications,
so scientists can develop better, safer drugs Test drugs on animals and humans to ensure safety and efficacy
Determining the most effective formulation and dosage for a specific drug
Working on improving the drug manufacturing process Ensuring the consistent quality of prescription
medications Advising corporations or government agencies, including the
Food and Drug Administration, on issues related to pharmaceutical development
Monitoring drug adverse reactions And many more areas....
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CONCLUDING REMARKS The discovery or isolation of the drug, whether it is a small or
large molecule is an exciting but a complex process of studying its structure (along with thousand of related structures), mechanism of action, and physicochemical properties
Safety and Efficacy are main concerns in Preclinical & Clinical phases; CMC is the subject of API & formulations
Pharmaceutical R&D scientists come from a vast array of specializations within health sciences, chemistry and biotechnology majors
Specializations can be very refined and narrowly focused these days
Industry, Government and Academia are main employers Adaptation and continued education are key factors of success Big Pharma & the Pharmaceutical-Biotech Ecosystem (PBE) are
the career builders & sustainers in general 25