Showing posts with label FDA. Show all posts
Showing posts with label FDA. Show all posts

Thursday, October 20, 2016

FDA/CMS: New Administration, New Challenges?

Knect365 FDA/CMS Summit, photo on-site
photo credit: @KimTweetsDC

For over 20 years we have been working hard on delivering you with first-hand insights into one of the most heavily-regulated industries in the world.

With recent debates over drug pricing, the FDA is faced with some challenges over regulation policies to ensure the healthy balance of big pharma companies on the market.


Here are the main three questions that are bugging the minds of the Top Biopharma Executives today:


• What does the future hold for the Affordable Care Act and health reform in the post-Obama landscape?
• What is the state of biosimilars in the US, and how these medicines may impact the cost curve for biologics as more reach the market and uptake becomes measurable?
[read an excerpt from the panel discussion with experts from Mylan, Pfizer and Momenta Pharmaceuticals “Biosimilars are here. Now what?”.]
• Transparency around pricing.

Do these topics keep you up all night as well?

Be the first one to learn the updates directly from CDER and CMS right in the heart of DC, the political epicenter of the United States at the 11th Annual FDA/CMS Summit.


Some of the themes to be discussed at the Summit include:


• An overview of regulatory and policy news;
• Regulatory & reimbursement expertise from KaloBios Pharmaceuticals Inc., FDA, REGENXBIO, Aimed Alliance, Acorda Therapeutics, Beth Israel Deaconess Medical Center, and many others;
• The state of biosimilars and revisions to BSUFA;
• Drug Development Innovation including regulatory strategies of pandemics such as Ebola and Zika.

For the full range of topics download the brochure here.

Join an open dialog over the industry issues with other health care professionals from the FDA and CMS regulatory agencies, including Janet Woodcok, Gerald Dal Pan and John Jenkins at the FDA/CMS Summit, this December, 14 – 15th in Washington, DC.

As a valued member of our community you can register with a special discount of $100 OFF the current rate using this code: PFDA16SOCIAL.

Secure your spot and the best rate here.



Stay tuned:



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Friday, June 3, 2016

Creating New Pathways for the Development, Translation, and Delivery of Immunotherapies


The team behind the Next Generation Protein Therapeutics Summit have recently produced an exclusive whitepaper titled "Creating New Pathways for the Development, Translation, and Delivery of Immunotherapies". Below you will find a brief summary of the whitepaper and download the complete whitepaper now


 Whitepaper Summary:

The last decade has seen substantial growth of immunotherapy treatments for cancer. The new immunotherapies have produced exciting results in terms of response rates to treatment for certain cancers, such as melanoma, which have been refractory to treatment, once substantial metastasis has occurred. The US Food and Drug Administration (FDA) has approved several antibodies against immune checkpoint inhibitors based on the encouraging results in clinical trials. Other types of immune therapies are also being developed which may also be useful in the treatment of cancer.

New antibody/cytokine fusion proteins, anti-CD 137 monoclonal antibodies (mabs) for stimulating cells of the immune system, more refined uses of cytokines in immunotherapy treatments, cancer vaccines, use of genetically engineered T cells to specifically target tumors, new techniques in stimulating the innate immune system and combinations of immunotherapies have great potential for being effective treatment options for cancer treatment in the future.

Challenges, however, remain to perfect these therapies for use in the clinic for cancer treatment. The nature of these challenges are scientific, clinical and regulatory. Scientific challenges include defining the appropriate tumor types for an appropriate immunotherapy, the conditions under which various cells of the immune system would be activated and determining how best to manipulate them to allow for maximum tumor cell destruction, finding better ways to circumvent cancer cell suppression of immune cell responses and using new techniques to prevent or ameliorate the nonspecific injury to normal tissue that can occur as a side effect of immunotherapeutic treatment.

Clinical challenges include ensuring there is adequate quality control in manufacturing process to supply the agent in pure enough form for clinical trials, obtaining enough patients that meet inclusion criteria, designing clinical trials that will yield adequate information to assess the safety and efficacy of the treatment and defining appropriate endpoints for a cancer clinical trial to effectively interpret clinical data gained from the clinical trial.

Regulatory challenges can occur at multiple levels for companies or entities trying to gain FDA approval for their immunotherapy technique or product. These challenges can be at the preclinical level, clinical or manufacturing levels. Adherence to regulations governing Good Laboratory Practices, Good Clinical Practices, and Good Manufacturing Practices can be problematic when trying to take immunological reagents or cellular treatments from the research laboratory to the cancer treatment clinic.

Despite the challenges when conducting research and treatment with immunotherapies, the intense level of research and data being generated with immunotherapies for cancer will ensure that a wide variety of new therapies will be possible in the coming years.




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Friday, August 7, 2015

This Week in BioPharma: 8/3-8/7

Here is the top news from the biopharmaceutical industry this week:

Biotechnology is helping to heal Delaware: Nearly 22,000 women will be diagnosed with ovarian cancer this year. Another 14,000 will die from the disease. One Delaware biotech firm is working to change that. In December, Wilmington-based AstraZeneca Pharmaceuticals released Lynparza, a new medicine for women with advanced ovarian cancer. Innovative treatments like Lynparza help Delaware patients live longer and healthier lives. Drug development also keeps Delaware's economy healthy by creating jobs and supporting local businesses. But now, Congress may jeopardize the health of our state and its residents with ill-advised changes to Medicare Part D and patent laws. Read the full post here.

U.S. officials warn medical devices are vulnerable to hacking: The federal government is warning about a medical device that could be tampered with by hackers. The FDA and Department of Homeland Security issued a statement that "strongly encourages" health care facilities to discontinue the use of Hospira's Symbiq infusion pump after officials learned the devices are vulnerable to cybersecurity threats. The medical device company confirmed that the computerized pumps -- which continuously deliver medication over an extended period -- could be accessed remotely through a hospital's network. This could allow an unauthorized user to control the device and change the dosage of medication the pump delivers to a patient. Read the full post here.

Allow medical devices sector to work with doctors: Pitching for allowing medical devices industry to engage doctors, industry body CII today said preventing medical practitioners to undergo training about latest technologies may be detrimental. Currently, under the voluntary the Universal Code for Pharmaceutical marketing Practices (UCPMP) industry is not allowed to engage medical practitioners for continued medical education on latest technologies, CII said in a statement. "Medical Device Industry is an innovation driven industry and needs to work with medical practitioners as well as paramedical professional in close proximity," the industry chamber said.  Read the full post here.

How can we derisk innovation in pediatric medical devices?: Sometimes, kids need intensive medical treatment – and the tools used for adults aren’t necessarily suitable to treat smaller, growing bodies. This presents a unique challenge for surgeons and clinicians, who find themselves with limited options when treating sick children. That’s where the Sheikh Zayed Institute for Pediatric Surgical Innovation comes in. It’s a division of the Washington, D.C.-based Children’s National Health System – and focuses on making pediatric surgery more precise, less invasive and, ideally, pain-free. Kolaleh Eskandanian, executive director of the Institute, spoke with MedCity News about the unique challenges in pediatric medical device innovation – and ways they’re helping jumpstart entrepreneurship in this small but important market. Read the full post here.


Technavio Says the High Demand for Biopharmaceuticals Will Inflate the Global Single-use Bioprocessing Systems Market Through 2019:  Technavio has published a new report on the global single-use bioprocessing systems market, which is expected to grow at a CAGR of more than 34% from 2015-2019. The new report indicates the increase in the aging population is leading to a rapid increase in patient population suffering from diseases such as diabetes, hypertension, musculoskeletal and cardiovascular diseases, chronic kidney diseases, cerebral strokes, and cancer. This increases the demand for biopharmaceuticals among patients. Read the full post here.


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Wednesday, February 11, 2015

[Video] Breakthrough Status: Are You Ready?

In today's featured presentation from TIDES 2014, Jeffrey Baker, Ph.D., Deputy Director, Office of Biotechnology Products, Center for Drug Evaluation and Research, U.S. Food and Drug Administration talks about FDA SIA (Safety and Innovation Act). He presents a rundown of this act and talks about NDAs (Non-disclosure agreement), and BLAs (Biologics License Applications). Baker states that FDA SIA has made available a pathway for rapid approval of drugs critical to public health, however companies need to be prepared to manufacture and meet patient needs. Are you ready? For details, watch the presentation:



TIDES 2015 will take place May 3-6, 2015 in San Diego, California.  This year, Ravi S. Harapanhalli, Ph.D., Vice President, Technical, PAREXEL International and Former Branch Chief, Office of New Drug Quality Assessment, US FDA, will be on hand to present Progress in Advancement of RNAi Therapeutics.  For more information about this session and the rest of the program, download the agenda.  As a reader of this blog, when you register to join us and mention code XB15180BLOG, you can save 20% off standard rates.


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Wednesday, November 26, 2014

Cyber Monday starts early! See details on how you can save on all IIR and IBC Events!

 


To get a head start on the holiday season, as a member of our online community, we’re giving you an extended chance to take advantage of our Cyber Monday sale. Register for the following event and receive 30% off the standard rates. Mention code CYBER2014 when registering for the following:

IBC’s Vaccine Development & Production Summit
December 8-9, 2014 in Boston, MA
Disease and Pandemic Vaccine Research, Discovery and Innovation
More about the event:
Register here.

IBC’s Antibody Engineering & Therapeutics 
December 7-11, 2014 in Huntington Beach, CA
The #1 Forum for Academia and industry to Connect for Scientific Exchange and Networking in Antibody Engineering & Therapeutics, lmmunobiology and Next-Generation Binders
More about the event.
Register here.

IBC’s Commercialization of Cell, Gene & Immunotherapies
December 11-12, 2014 in San Diego, CA
Accelerating the Translation of Commercially Viable Cell, Gene and Immunotherapies Through bioprocess Tools and Technologies
More about the event:
Register here:

IIR’s FDA/CMS Summit for Biopharma Executives
December 11-12, 2014 in Washington, D.C.
Hear about the commercial outlook for biopharma under the new health care exchanges.
More about the event.
Register here.

 IIR’s 19th Annual Drug Delivery Partnerships 
January 29-30, 2015 in Boca Raton, FL.
Accelerating the path to market by leveraging new partnerships, breakthrough innovation and unique business models. Visit the website for full details.
More about the event.
Register here.

IIR’s 12th Annual Medicare Congress
February 3-5, 2015 in New Orleans, LA
Survive the toughest rate environment to date with lessons from top-notch healthcare executives
Visit the website for full details.
Register here.

ePharma **
February 24-26, 2015 in New York, NY
Charge up your marketing campaign with ROI-infused initiatives and embody the newest technologies that bleed success
More about the event.
Register here.

IBC’s Genome Editing Applications
March 18-19, 2015 in Boston, MA
Don't miss out on the only event in the industry focusing on applications of genome editing technologies in research, drug discovery and therapeutic development.
More about the event.
Register here.

IBC’s Biopharmaceutical Development & Production Week (BDP)
IBC’s Single-Use Applications for Biopharmaceutical Manufacturing
IBC’s Flexible Facilities Conference
March 30 – April 1 in Huntington Beach, CA
Create Unique End-to-End Bioprocessing Solutions that Guarantee Reproducible Results and Commercial Manufacturing Success
More about the event.
Register here.

IIR’s 24th Annual Partnerships in Clinical Trials
April 22-24, 2015 in Boston, MA visit the website for full details.
Accelerate speed to market by leveraging new partners, new technologies, and new business models at the must-attend clinical event of the year
More about the event.
Register here.


TIDES
May 3-6, 2015 in San Diego, CA visit the website for full details.
The #1 Industry Forum for CMC, Clinical and Discovery Professionals to Accelerate Oligonucleotide and Peptide Product Development
More about the event.
Register here.

Have any questions? Email Jennifer Pereira.

*This promotion is only valid Wednesday, November 26th 2014 through Monday, December 1st  2014. Offer cannot be applied retroactively to confirmed paying registrants and cannot be combined with any other discounts or promotions. All registrants and guests are subject to IIR approval.
**Cyber Weekend offer only applicable to registrants not utilizing the Buy One Get One offer. Only pharma/biotech/med device companies are eligible for The Buy One Get Offer


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Wednesday, November 19, 2014

Creating A New FDA/Capitol Hill Legend

Via RPM Report, an FDA/CMS Summit for Biopharma Executives event supporter. The RPM Report provides actionable insight on regulation, policy, FDA and CMS to apply directly to your decision-making.

When FDA managers reflect on their experiences on Capitol Hill, the stories often involve unfair, inflammatory or downright abusive sessions. But Center for Drug Evaluation & Research Director Janet Woodcock has built a different legend this year during the 21st Century Cures initiative of the House Energy & Commerce Committee.

CDER Director, Janet Woodcock has pulled off a Capitol Hill miracle during the 21st Century Cures review of the issues affecting drug and medical device development and commercialization, being the regulator embraced by both sides of the aisle.

From start to finish, Woodcock has basked in praise from Republicans and Democrats. But those notes of praise rose to a crescendo during the final, pre-election session hosted by the E&C/Health Subcommittee on Friday, Sept. 19. During a hearing focused on antibiotic development incentives, Woodcock engaged in a cordial farewell dialogue with the soon-to-retire Rep. Waxman (one of Democrats who traditionally has not been among her supporters), diplomatically handled more calls for FDA-based incentives for the development of antimicrobials and other drugs, and then received congratulations from Rep. John Shimkus (R-Ill.) who applauded Woodcock for staying to listen to the second panel of the hearing.

Incentives Entail Congressional Art, Not Opinions of FDA Scientist/Doctor

Based on her performances, Woodcock has earned the ability to defer opinions on flashpoint issues without looking like she was dodging the issue.

On the topic of incentives for drug developers based on FDA or by conferring exclusivity to a target category or to another drug chosen by the sponsor, Woodcock was able to avoid staking out a stance one way or the other, and instead referred to the criticisms of incentives raised by Waxman and noted that striking that type of balance falls in the realm of Congress and politics and to a physician and scientist.

She had few failures over the five-month period and none that seem to do damage to the agency’s improving reception on Capitol Hill.

Woodcock has so far been unable to see her idea of pushing improvement in drug quality and manufacturing as a jobs issue and a way to stimulate the US economy. That’s a big issue to Woodcock but a small down-note in an otherwise harmonious legislative season for the agency.

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Do you want the chance to hear from Janet Woodcock, other key regulators from the FDA and CMS, and industry game changers? Join them at the 10th Annual FDA/CMS Summit for Biopharma Executives this December 11-12, in Washington D.C.

At the event, Janet Woodcock will be addressing what the midterm congressional elections mean for the biopharma industry. Do not miss this!

Register here.


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Wednesday, November 12, 2014

Sovaldi: Shooting Star Instead of Blockbuster

Via RPM Report, an FDA/CMS Summit for Biopharma Executives event supporter. The RPM Report provides actionable insight on regulation, policy, FDA and CMS to apply directly to your decision-making.
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Gilead’s Sovaldi HCV treatment has earned a special place in pharma lore with its rapid rise to about $10 billion in sales (bringing with it lots of controversy about the sustainability of specialty drug pricing). Now the product appears poised to make a new reputation: fastest to fall from blockbuster status.
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The debate over what qualifies as a “blockbuster” drug is one of those inside-industry debates that has gone on—and will continue—for decades. There was a period when $100 million in annual sales earned a product “blockbuster” status, but that is long ago. The new thresholds are about ten times that level.   

No matter what sales trigger defines “blockbuster,” Gilead’s hepatitis C product Sovaldi is far above it. The brand should be remembered for decades as one of the fastest out-of-the-blocks blockbusters -- approaching $8 billion in sales in its first nine months of marketing.

However, Sovaldi may be gone just as fast – more like a flashing comet in the pharma firmament than a lasting blockbuster. The active ingredient, sofosbuvir, will not go away, but the single-ingredient brand is likely to become quickly irrelevant.

Gilead is preparing for FDA approval of the next-generation two-ingredient fixed dose oral combination product to supplant Sovaldi on October 10. That product will have treatment success rates, pricing, convenience and patient-experience qualities that should mean that Sovaldi will recede from the market with something approaching a mirror image of its meteoric rise.

After remaining relatively quiet in public during the months of shock and push back from the payer community about the pricing of Sovaldi at $84,000 for a typical course of therapy, Gilead has begun to speak out in advance of the upcoming launch of the ledipasvir/sofosbuvir combo (called Harvoni in Europe).

Gilead President John Milligan explained the pricing for the new product to the DC policy world at an Oct. 1 Brookings/Engelberg Center half-day session on the “Cost and Value of Biomedical Innovation.” That discussion complemented other conversations with the financial community and presumably with payers who should be more prepared for the follow-on product than for Sovaldi.   

Milligan said the new product will priced in line with the total drug current treatment costs for existing 12-week Sovaldi /PEGinterferon/ribavirin treatment, or roughly $94,500.

That means the new combo will cost about $10,000 more than Sovaldi as a single ingredient per treatment course but the added cost will reflect a shift of PEGinterferon/ribavirin costs to the combo drug and not added costs for the drug regimen part of the HCV treatment. With the new ingredient, Gilead will capture the part of drug costs going to other manufacturers for PEGinterferon and ribavirin.   

Milligan, in fact, argued that pricing to the total cost of current standard of care is the foundation of Gilead’s pricing decisions – and, he suggested, the industry‘s standard practice.

“At the end of the day,” Milligan said, “the pricing analysis [for the original launch of Sovaldi] was  relatively simple – current cost of other therapies.” Responding indirectly to the months of outside speculation on the factors considered in Sovaldi pricing, he said that Gilead “didn’t look at return on investment; we don’t look at sunk costs. None of that goes into our pricing.” Generalizing to the industry, Milligan said, “in fact, I don’t know a single firm that uses that as a metric for how to determine [price].”

So, with the combo removing the tough PEGinterferon and ribavirin pieces of treatments, the need for Sovaldi as a single ingredient should quickly diminish.

Milligan described Sovaldi numerous times (at least three times) in his short Brookings presentation as a “stop-gap” therapy that Gilead developed to get to the market first to meet demand for a higher efficacy HCV treatment -- beyond the big improvements previously offered by Vertex’s Incivek and Merck’s Victrelis.   

“We worked very hard,” Milligan said, “to bring in Sovaldi as a stop gap between where we were with very difficult interferon-containing regimens to the future which will be all-oral regimens.”

So, the blockbuster was really a “stop-gap” to the sponsor.

Maybe looked at in retrospect, it was also a stalking horse – to acclimate the market to the single-ingredient  price and then make the two-ingredient fixed combination look more attractive. That may explain Gilead’s reticence for fighting back on the response to Sovaldi pricing: not only was the product doubling the size of the company, it was creating a better milieu for the more important next product.

Starting the fixed dose combo at the same price as current 12-week Sovaldi plus injections therapy has three other important benefits to Gilead.

1. It sets up the potential of a reduced treatment price for the fixed dose combo when used in a shorter, 8-week treatment regimen for less severely ill patients – thus making it harder for payers to try to limit use to only the sickest patients. The less sick patients will be expensive to treat but enough less expensive than the 12-week therapies that the payers should feel pressure.

2. It creates less room for pricing decisions by the next-comers (like Abbvie’s four-ingredient ABT-450 product which appears on track for an end of 2014 approval decision form FDA).  There is obviously room for price strategies under $94,500 for twelve weeks and $63,000 for eight-week therapy. But by keeping the price close to current costs, Gilead is leaving next competitors less options.

3. Finally, and this is another reason that Sovaldi as a brand may be remembered as a comet rather than a blockbuster, sofosbuvir as a single agent quickly was gaining an important place in an unapproved two-product combination in clinical practice, paired for treatment of about 40% of people getting HCV treatment with the Janssen product Olysio (simeprevir). Together, the two products cost about $150,000 at wholesale acquisition cost, Milligan told Brookings. He described that as “a very expensive regimen,” implying that Gilead could have considered that as the benchmark for its combo, but didn’t.

By pricing a third lower than that existing oral combo, Gilead will look more responsible with its new product. And Sovaldi will be the bright comet that was.

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Come to the 10th annual FDA/CMS Summit for Biopharma Executives to find out more about these issues and many more plaguing the industry. Our keynote speakers and panels will take a deep dive into each of these topics, and more. You'll leave better able to make strategic decisions on issues such as:

• The commercial outlook for biopharma under the new health care exchanges

• Updates on the latest drug review statistics from the Office of New Drugs and industry's experience under the new review "Program"

• The future of drug safety at FDA — both for the increasingly popular rare disease drugs as well as new treatments for large primary care markets like obesity and diabetes

• What's in store for the reauthorization of PDUVA VI, and a preview of what's to come as industry and FDA take a second look at BsUFA and GDUFA.

• Coming changes to Medicare Part D and what CMS has in store for the prescription drug benefit

• What the mid-term Congressional elections will mean for the biopharma industry.

Register now and join us at the Fairmont Washington DC, December 11-12, 2014 for this can’t-miss event.



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Wednesday, November 5, 2014

Last Chance to Save $200 for FDA/CMS Summit for BioPharma Executives | Early Bird Rate Ends Friday


What do payors want when it comes to biopharma policy? Come to the FDA/CMS Summit for BioPharma Executives, December 11-12, 2014 in Washington, DC to hear payor perspectives on biosimilars, drug pricing, FDA reforms and drug coverage under Medicare, Medicaid and in the new Affordable Care Act Exchanges.

Take advantage of our Early Bird Rate, a savings of $200 off the standard registration rate. Register now.


Our keynote speakers and panels will take a deep dive into each of these topics, and more. You'll leave better able to make strategic decisions on issues such as:

• The commercial outlook for biopharma under the new health care exchanges

• Updates on the latest drug review statistics from the Office of New Drugs and industry's experience under the new review "Program"

• The future of drug safety at FDA - both for the increasingly popular rare disease drugs as well as new treatments for large primary care markets like obesity and diabetes

• What's in store for the reauthorization of PDUVA VI, and a preview of what's to come as industry and FDA take a second look at BsUFA and GDUFA.

• Coming changes to Medicare Part D and what CMS has in store for the prescription drug benefit

• What the mid-term Congressional elections will mean for the biopharma industry.


P.S. Maximize your investment by also attending the co-located FDA/CMS Summit for Payers. If you purchase the All Access Pass you will be able to not only collaborate with biopharm exeuctives, but rub elbows with C-Level health plans executives as well. Register now so you can double the speakers, double the content, and double the value for only an additional $800! Use the code XP1917BLOG when getting your All Access Pass to save $100, making it only an additional $700!

Register Here.

If you have any questions about the event, please reach out to Ryan Geswell at rgeswell@iirusa.com


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Wednesday, October 22, 2014

Introducing the FDA/CMS Summit for Biopharmaceutical Executives

Join us for the 10th Annual FDA-CMS Summit, for biopharmaceutical executives, December 11-12, 2014 in Washington, DC. Our keynote speakers and panels will take a deep dive into each of these topics, and more. You'll leave better able to make strategic decisions on issues such as:

• The commercial outlook for biopharma under the new health care exchanges

• Updates on the latest drug review statistics from the Office of New Drugs and industry's experience under the new review "Program"

• The future of drug safety at FDA - both for the increasingly popular rare disease drugs as well as new treatments for large primary care markets like obesity and diabetes

• What's in store for the reauthorization of PDUVA VI, and a preview of what's to come as industry and FDA take a second look at BsUFA and GDUFA.

• Coming changes to Medicare Part D and what CMS has in store for the prescription drug benefit

• What the mid-term Congressional elections will mean for the biopharma industry.

 
Speakers Include:

o Janet Woodcock, MD, Director, Center for Drug Evaluation and Research (CDER) Food and Drug Administration (FDA)
o John Jenkins, MD, Director, Office of New Drugs, Food and Drug Administration (FDA)
o Leah Christl, Associate Director, Biosimilars Program, Office of New Drugs Food and Drug Administration (FDA)    
o Gerald Dal Pan, MD, Director, Office of Surveillance & Epidemiology, Food and Drug Administration (FDA)
o Jim Robinson, President, Astellas Pharma US    
o Sumant Ramachandra, MD, PhD, MBA, SVP & Chief Scientific Officer, Hospira
o Robert Clark, VP, US Regulatory Affairs, Novo Nordisk    
o Francois Nader, MD, CEO, NPS Pharmaceuticals
o Karen Jones, VP, Global Head of Oncology Regulatory, Genentech    
o Chris Garabedian, CEO, Sarepta
o David Beier, Partner, Bay City Capital    
o John McHutchison, MD, Executive Vice President, Clinical Research, Gilead
o Mark McClellan, MD, PhD, Senior Fellow and Director, Health Care Innovation and Value Initiative, Brookings Institution    
o Niall Brennan , Acting Director, Office of Enterprise Management, Centers for Medicare & Medicaid Services (CMS)
o Tamara Syrek Jensen, JD , Deputy Director, Coverage and Analysis Group, Office of Clinical Standards and Quality, Centers for Medicare & Medicaid Services (CMS)    
o Mark McCamish, MD, PhD, Global Head Biopharm.& Oncology Injectables Development, Sandoz International GmbH
o Karen Jones, VP, Global Head of Oncology Regulatory, Genentech    
o Chris Garabedian, CEO, Sarepta
o David Mott, General Partner, Biopharmaceutical Investments, New Enterprise Associates (NEA), Former CEO, MedImmune    
o Steven Nissen, MD, MACC, Chairman, Department of Cardiovascular Medicine, The Cleveland Clinic Foundation

Register now for this can't-miss event! 


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Friday, October 10, 2014

Approaching Quality of Biopharmaceutical Manufacturing at the Highest Level

In today's featured interview from Biopharmaceutical Development and Production Week 2014, Jeffrey C. Baker, Ph.D., Deputy Director, Office of Biotechnology Products (OBP), Center for Drug Evaluation and Research, U.S. FDA talks about the challenges in the bio processing industry, the systems based thinking facing the industry and knowledge management, He also looks at the challenges facing the industry, the future of regulation of continuous process validation, He also addresses how global supply chains can help the needs of the patients. Want to learn more?

Watch the interview here:


To hear more exclusive insights from biopharmaceutical production regulators, join us at the 2015 Biopharmaceutical Development and Production Week. It will take place March 30-April 2 in Huntington Beach, California. To receive updates on the program as they occur, sign up for email updates.



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Thursday, October 2, 2014

Analytics for Modern Bioprocess Development

Today, we feature an article from our partners at BioProcess International Magazine. This is an excerpt from the article Analytics for Modern Bioprocess Development.


Like most other industries growing within the rapidly changing information era, the bioindustry is generating more data than it ever has before. But meaningful information — that which can be linked to process knowledge and, ultimately, process control — is useful only with a robust and efficient data acquisition system. As Gernot John (director of marketing and innovation at PreSens) observes, the underlying factors supporting improved data acquisition in the industry include an increased interest in switching from offline to online measurements, scalability (miniaturization) of analytical instrumentation, and the ongoing change from analog to digital signal transmission.

“Determining the type of process data you need to evaluate — whether it’s quality data, discrete, or online measurements, and/or batch-record data — begins by asking ‘What are we trying to achieve?’” notes Justin Neway, PhD (general manager, operations intelligence and senior fellow, Accelerys Science Council, at Accelrys). He identifies at least four drivers in the need for process informatics. The first is a need to reduce process variability by improving process understanding (which is the touchstone of PAT and QbD), implementing robust design processes, and using online instrumentation. “When QbD came out, it started to sound a bit more pragmatic than PAT. Then the industry started to see the connection between it and PAT, and the industry began actually producing useful outcomes. Now, with the aim of process robustness, it becomes much more business oriented,” says Neway. He points out that a robust process reduces business risk by decreasing supply chain risk. It also can improve profitability and decrease patient safety issues and risks of 483s and FDA warning letters.

Another driver for process informatics is the need for transparency in outsourcing relationships. “That’s not just about cost. It’s about companies specializing in their core area,” says Neway. Much of the renewed emphasis on contract relationships stems from a 2013 FDA draft guidance on quality agreements (2) “The phrase I love in that document is that the FDA considers contractors ‘an extension of the manufacturer’s own facility’” says Neway. With that statement, the agency solidifies the union between sponsor company and contract organization — they are one in the same.

A third driver is the bioindustry’s need for collaboration. Certainly that applies to the partnership between a sponsor company and a contractor, but it holds true for internal collaborations as well. Those types of collaborations can be tough for two reasons, says Neway. “First: You need process development (where the process is designed and scaled up) to collaborate with quality (which takes the responsibility for minimizing risks to patients) and manufacturing (where the process is operated repeatedly at commercial scale and needs support from those who designed it). Second: You need to have those collaborations on a global scale. Email is not enough — you need an environment where people can dive in and work on the same data regardless of time zone, department, even what company logo they’re working under. That is one of the big drivers for process informatics”

The last is the bioindustry’s need for knowledge capture, transfer, and management. Experienced professionals are retiring from the industry, taking with them the process knowledge and expertise that much new hires still needs to embody. “That means knowledge needs to transfer from more-experienced people to less-experienced people as efficiently as possible,” says Neway. This last point is especially important for connecting the operations data and measurements data between, for example, quality laboratories working with laboratory information system (LIMS) and process batch-scale operations working with batch record systems and data historians. People tend to act in silos. “Their LIMS system is organized to identify and manage samples, test protocols, operators, standards, and provide reports of all the results of all the samples. It was not built with an organization that reflects the production process.”





You can find out more about topics like this and meet and network with other professionals in the bioprocessing field at this year's BioProcess International Conference and Exhibition.  As a reader of this blog, when you register to join us October 20-23 in Boston, you are eligible to receive 20% off the standard rate when you mention code BPI14BLOG.



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Friday, September 26, 2014

Perspectives on Assessment, Assurance and Drug Quality: Part 2

In today's featured presentation from Biopharmaceutical Development and Production Week 2014, Jeffrey C. Baker, Ph.D., Deputy Director, Office of Biotechnology Products (OBP), Center for Drug Evaluation and Research, U.S. FDA talks about Abbreviated License Pathway for biological products- which rely on “highly similar” FDA product on existing knowledge about the safety, purity, and potency of the reference product. He mentions that as of February 28, 2014, CDER had 62 requests for an initial meeting and how FDASIA makes it criminal to stay silent about counterfeiting or safety related issues.Baker states that the FDA has a focus on quality expectation for clinical performance.

Want to know more? Watch the interview here:


Watch Part 1.

Biopharmaceutical Development and Production Week will take place March 30-April 2, 2015 in Huntington Beach, California.  To get the latest updates on the 2015 program, sign up for email updates.


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Friday, September 19, 2014

Perspectives on Assessment, Assurance and Drug Quality

In today's featured presentation from Biopharmceutical Development and Production Week 2014, Jeffrey C. Baker, Ph.D., Deputy Director, Office of Biotechnology Products (OBP), Center for Drug Evaluation and Research, U.S. FDA talks about the FDA’s work environment is of assurance, assessment, and assertion, the space of assertion that a company has, process validation (making an assertion and being an advocate, in a data driven way),and the many ways to look at quality by using different tools to evaluate it. Baker stated that he believes that design is about providing an experience.

Want to learn more? Watch the first part of the presentation here:


Biopharmaceutical Development and Production Week is will take place March 30-April 2. The agenda will feature more unique insights into the regulations of biopharmaceutical production so be sure to sign up to receive program updates for the 2015 agenda.


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Tuesday, September 9, 2014

FDA Establishes New "Purple Book" for Biosimilars

It may not make the New York Times’ Best Seller List, but the release of the FDA’s new book is certainly noteworthy.  The FDA today announced that they’ve published their first ever edition of the “Purple Book”, a list of licensed biological products and interchangeable biosimilars. 

The organization’s new list will serve a similar role to that of its counterpart in the pharmaceutical industry, the Orange Book, and will look to answer questions around the substitutability of products.  Many have voiced concerns over the extent to which biologics and biosimilars will be used interchangeably.  Although aimed to replicate the biologics they’re designed after, biosimilars are not identical to those drugs and therefore are not necessarily perfect substitutes in all cases.
Purple Book Biosimilars Biologics FDA list licensed

The FDA has indicated that they will use a four part scale to categorize the interchangeability: 
  •         Not similar
  •         Similar
  •         Highly similar
  •         Highly similar with a fingerprint-like similarity

The book is broken up into two sections—biologic products regulated by the Center for Drug Evaluation and Research (CDER) and those regulated by the Center for Biologics Evaluation and Research (CBER). Among the information included in these lists is the date a biologic was licensed, the product name, the proprietary name and the BLA number. 

As we begin to see biosimilar applications roll in, we may see this list build out rather quickly over the next few years. 

You can find the announcement from the FDA here.

We’ll have more on the latest developments in the biosimilars market at the 15thAnnual Business of Biosimilars meeting. Join us October 20-22 in Boston, MA. Download the agenda to see what’s on tap.
                                                                                                     
SAVE $100.  Register here and use code XP1986BLOG.


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Thursday, September 4, 2014

Biosimilars: Seven Cold Hard Facts

On July 24th the FDA accepted its first application for a biosimilar drug in the U.S. and put the industry on alert that this new market is fast approaching.   While no one knows exactly when the first approval will come, here are a few facts to bring you up to speed for when it does: 

·        Estimates on savings attributed to biosimilars range from $42 - $108 billion over the first ten years of the market.

       The value of biologics slated to come off patent by 2017 is about $70 billion.

 Per the Rheumatology Network, over the span of their lifetime, many drugs approved in the US and EU have eventually become “biosimilars” of themselves.  This is due to a “natural drift” in drug properties caused by changes in production such as using different batches of medium or manufacture at different sites.

         Recently, a group of 19 investors representing nearly $430 billion in assets  commended Novartis and Amgen for supporting a set of investor principles to guide boards on activities related to biosimilars. 

      A survey conducted among senior’s organization RetireSafe shows that 92% were unaware that the Affordable Care Act potentially allows for biosimilar drugs to be substituted for a biologic.  Furthermore, this could potentially be done without the patient or doctor being aware.

 Hospira is looking to file its first biosimilar in the US within twelve months and currently has an R&D pipeline valued at around $40 billion.  

•  Amgen is developing a portfolio of biosimilars of which three are slated to launch in 2017.   

We’ll have more on the latest developments in the biosimilars market at the 15th Annual Business of Biosimilars meeting. Join us October 20-22 in Boston, MA.  Download the agenda to see what’s on tap.

SAVE $100.  Register here and use code XP1986BLOG.


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Tuesday, August 26, 2014

Doctors Take Sides on Biosimilar Naming Issue

Doctors have officially taken sides in the naming rights battle for biosimilars.  In a recent letter to the FDA, a group of physicians has taken the stance that biologic and biosimilar drugs should in fact have unique names.  This letter comes weeks after another piece of mail showed up at the FDA headquarters requesting that the agency not require distinct names for the two types of drugs.  The lobbying is part of a struggle between biologics manufacturers who want to protect their brand equity by requiring separate names and potential biosimilar manufacturers wanting to piggy back off that equity by using the original drug names for their products.

The letter, signed by 23 different physicians, claims that no matter how similar drugs might be, they can cause different reactions among patients with similar diagnosis’ and physical traits.  Distinguishing between the drugs is key and the group feels similar names could get in the way of that.   

Biosimilar naming: Doctors have  drawn a line in the sand“A biosimilar will only be similar, but not identical to the reference product for the foreseeable future. Distinct nonproprietary names will help to alert physicians that each product, while safe and effective, may differ slightly,” the group writes to the FDA.  “Rather than deter physicians from prescribing these products, we believe that allowing physicians to know the exact product that they are prescribing will increase confidence, thus encouraging more robust utilization of biosimilars than may develop without this transparency.”

A recent survey found that in the Europe (where a robust biosimialr market already exists), 61% of physicians prescribing biologics or biosimilars were of the understanding that if two products shared an international non-proprietary name, they were approved for all of the same indications. 

Other lobbying efforts on this policy include a number of petitions submitted to the FDA over the last few weeks.  While the organization has been mum on a possible decision, the market may push their hand sooner rather than later.  Two drug makers are already seeking regulatory permission to sell certain medications meaning that at least one biosimilar could become available next year. 

Until then, the letters and petitions will likely continue to fill the mailboxes at the FDA’s headquarters.

Want more on the latest in the biosimilars industry? Join us for the 15th Annual Business of Biosimilars meeting, October 20-22 in Boston, MA.  Download the agenda to see what else is on tap.

SAVE $100. Register here and use code XP1986BLOG.

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Tuesday, August 19, 2014

FDA Tentatively Approves Lilly's New Diabetes Medication

The FDA has granted Eli Lilly “tentative” approval for a diabetes medication akin to Sanofi’s Lantus.  The drug, to be marketed as Basaglar, is a long-lasting insulin injection that helps to control blood-sugar levels and is essentially a knockoff of the Sanofi version.

The new medication, however, won’t reach shelves for at least 30 months as Sanofi has filed a suit claiming patent infringement.  The drug could hit the market earlier if the court rules in favor of Eli Lilly but is in a holding pattern until then.  Lantus is scheduled to come off of patent February of next year.  This news comes months after Merck divulged plans to develop its own knockoff of the diabetes medication. 

Basaglar has the same amino acid sequence as Sanofi’s drug but for technical reasons is not considered a biosimilar—although for all intents and purposes, it is one.  By European standards, the drug does actually fall under the biosimilar classification and goes by the name Abasria.    

Said Christophe Arbet-Engels, Vice President, Metabolic-clinical Development and Medical Affairs, Boehringer Ingelheim Pharmaceuticals, Inc., "Because of the combined diabetes, development and commercialization experience of Lilly and Boehringer Ingelheim, we are confident that Basaglar, upon final approval, will become a valuable treatment choice for people who need a basal insulin to manage their type 1 or type 2 diabetes."


The biosimilars news is going to keep coming. We’ll have the breakdown of the latest industry updates and trends at the Business of Biosimilars conference. Join us October 20-22 in Boston, MA. Download the agenda here to see what’s on tap.

SAVE $100Register here and use code XP1986BLOG.

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Thursday, August 14, 2014

Higher-Order Structure Comparability: Case Studies of Biosimilar Monoclonal Antibodies

Today, we feature an article from our partners at BioProcess International Magazine. This is an excerpt from the article Higher-Order Structure Comparability: Case Studies of Biosimilar Monoclonal Antibodies.


For successful development and marketing of biosimilars with desired efficacy and safety, this industry recognizes the central importance of extensive analysis comparing innovator and biosimilar molecules. It is also recognized in the biotechnology arena that our understanding of complex biologics remains limited even though we have many analytical technologies available to us. A recent FDA guideline for biosimilar development states the following:

The three-dimensional conformation of a protein is an important factor in its biological function. Proteins generally exhibit complex three-dimensional conformations (tertiary structure and, in some cases, quaternary structure) due to their large size and the rotational characteristics of protein alpha carbons. The resulting flexibility enables dynamic, but subtle, changes in protein conformation over time, some of which may be absolutely required for functional activity. . . At the same time, a protein's three-dimensional conformation can often be difficult to define precisely using current physiochemical analytical technology. (2)

With an understanding of our current capabilities in biologics higher-order structure (HOS) characterization, we developed an antibody array enzyme-linked immunosorbent assay (ELISA) to provide a new approach for evaluation of MAb HOS.

In a previous report, we showed that antibody arrays developed specifically toward marketed MAbs could detect structural differences that correlated well with other analytical readouts, including bioassays and glycosylation analysis (8). Experiments have shown that antibody arrays can detect subtle changes that sometimes were not detected by bioassays or any other analytical technologies currently available.

The arrays use more than 30 polyclonal antibodies to cover an entire MAb molecule, thereby measuring its surface-epitope distribution systematically and sensitively, whereas other assays measure only part of the molecule or give an average status of a biologic's population. So antibody array technology should be able to provide a unique measurement of biosimilar MAb HOS comparability. We suggest that additional surface exposure from a baseline readout be termed conformational impurity(8).

Another advantage for antibody array technology is its ability to quantify small amounts of conformational impurity using an easy-to-operate ELISA format. As little as 0.1% conformational differences could be detected from all areas covered by the polyclonal antibodies, thus providing for accurate and sensitive measurement of the status of a MAb's conformation. No data yet correlate the impact of conformational impurity with efficacy and safety of a biosimilar MAb. But it is reasonable to postulate that more conformational impurities (epitope exposures) would increase the risk for potential immunogenicity if those additional epitopes were originally inside the innovator MAb molecule, which has been proven to be tolerated by patients’ immune surveillance systems. A significantly different new epitope exposure could break self-tolerance to a MAb and induce immunogenicity. Furthermore, increased exposure of new epitopes raises the possibility of a biosimilar MAb interacting with other regulatory proteins in a patient's body, causing off-target effects.

Read the full article and see detailed illustrations here.



You can find out more about manufacturing process and meet and network with other professionals in the bioprocessing field at this year's BioProcess International Conference and Exhibition.  As a reader of this blog, when you register to join us October 20-23 in Boston, you are eligible to receive 20% off the standard rate when you mention code BPI14BLOG.





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Monday, August 11, 2014

Biosimilars Can Save Money and Lives. Why the Delay?

Biologic drugs are used to treat a number of serious, life threatening diseases and save countless lives.  They are, however, exceedingly expensive.  The average daily cost of a biological in the U.S. ($45) dwarfs that of chemical drugs ($2).  Annually, some of these drugs can cost patients as much as $400,000.  The question becomes “how do we make these treatments more sustainable?”  The short answer to that question centers around biosimilars as one study estimates they have the potential to save north of $250 billion from 2014 to 2024. 
 
The long answer to that question, however, is not as straight forward.  Manufacturers of biological drugs can continue to charge monopoly prices as long as those drugs remain under patent protection.  Even as these medications begin to come off patent, many over the next few years, the road for biosimilars to enter the market is not exactly paved.  While many other countries (Australia, Canada, and the EU specifically) have had a market for biosimilars since 2006, the US policy for entry of these drugs remains ambiguous. 

Biosimilars Money Savings Patients FDA Cost Drug Biologics
A big part of this delay can be attributed to the FDA’s lack of progress in establishing guidelines for the approval of biosimilars.  Although they did accept their first biosimilar application last week, there still lacks a definitive set of regulations.  Tentative guidelines had been provided both in 2012 and 2014 but a final set is still in progress. 
This uncertainty in the regulatory process has caused apprehension among many drug companies and left fewer players vying for a place in the market.  Said one pharmaceutical executive, “I would like absolute clarity before we make a large investment. The quality of the decision is worth more than speed.”

While the FDA wavers in putting a process in place, biologics manufacturers have engaged in stall tactics.  The longer biosimilar drugs stay off the market, the longer these companies can continue to enjoy massive profits—reportedly as much as $100 million a month for some drugs.  The latest strategy employed involves disputing the naming system to be put into place for these drugs.  Biologics manufacturers have lobbied to maintain separate names, and the equity that goes with those names, from competing biosimilars.

While this dispute carries on, patients are missing out on billions of dollars in savings.  Many have called for the FDA to re-calibrate their priorities and fast track a set of guidelines that would allow biosimilars to hit the market sooner.  Other countries have had regulations in place for almost eight years while we wait for officials to perfect ours.  Until then, drug companies will continue to pad their pockets with massive profits from these drugs.   

Biosimilars is projected to be a lucrative industry. Can you afford to miss out? We’ll have the latest industry news and trends at the Business of Biosimilars conference. Join us October 20-22 in Boston, MA. Download the agenda here to see what’s on tap.

SAVE $100Register here and use code XP1986BLOG.

Follow us on Twitter: @FutureOfBiopharma & @Biosimilars
Join us on LinkedIn




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