Showing posts with label drug delivery. Show all posts
Showing posts with label drug delivery. Show all posts

Wednesday, April 20, 2016

Australia's Future in Global Peptide Drug Development


Paul Watt, Chief Scientific Officer, Phylogica Ltd, Australia sat down with the TIDES team to discuss the future of global peptide drug development in Australia as well as the current challenges for intracellular drug delivery and the important roles that academic institutions have in the development and commercialization of peptide therapeutics. Below you will find a brief excerpt from this exclusive interview. To access the complete interview, click here.


In terms of investment and innovation, where do you see Australia's future in global peptide drug development?

Australians have had a long history in peptide discovery. For example the pioneering work of Professor Mario Geysen enabled the parallel synthesis of peptides in the early 80's. More recently Australia has accumulated multiple high achieving peptide scientists such as Paul Alewood (eg. synthesis toxin peptides including use of selenolanthionine bridges), Richard Lewis and Glenn King (ion channel active venom peptides) (including ion channel inhibitors). David Craik (cyclotides and structural biology of complex peptides), John Wade (neuropeptides/relaxins). Australian peptide innovation has been successfully commercialised with the establishment of multiple companies, including Mimotopes, Auspep, Protagonist and Phylogica. As many of these companies mature, I see a bright future in the development of the Australian peptide industry. In addition several peptides discovered in Australia have been subject of multiple alliances with big Pharma offering further commercial potential as they progress through clinical development.


To learn more from Paul, join him at TIDES, May 9-12, 2016 in Long Beach, CA. Where he will be discussing how to design oligonucleotides with better drug-like properties to accelerate your products from discovery/preclinical to the clinic and to market.  

Register for TIDES now and save $100, use the code B16180BLOG100.


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Wednesday, March 11, 2015

Advances in siRNA Developing Delivery Solutions

In today's featured interview from TIDES 2014, Jared A. Gollob, M.D., Vice President, Clinical Research, Alnylam Pharmaceuticals, Inc. discusses exciting advances in siRNA.  He says there are several different delivery formulations and the company goes after targets they have confidence in.  He also talks about focusing on moving siRNA therapies into Phase III trials.  To learn more, watch the interview:


TIDES 2015 will take place May 3-6, 2015 in San Diego, California.  This year,John Maraganore, Ph.D.; Chief Executive Officer, Alnylam Pharmaceuticals, will be giving the keynote presentation Strategies and Challenges in the Development of Oligonucleotide and Peptide Drugs: Perspectives on DrugDevice Combinations and Drug Product.  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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Friday, August 15, 2014

Complex Medicines & Global Drug Delivery

In today's featured interview from Biopharmceutical Development and Production Week 2014, Tina M. Larson, Senior Director, Technical Development Operations & Engineering, Genentech talks about the four major opportunities in the drug delivery industry, and challenges in this industry. The four major opportunities include: improving drug-delivery to improve outcomes for patients, developing more complex medicines for patients, improving facility design and improving consistency for these drugs. She states that a challenge in this industry is delivering sophisticated medicines. She also says one opportunity in this industry is to scale these medicines globally. To learn more check out this interview:



Biopharmaceutical Development and Production Week will take place March 30-April 2 in Huntington Beach, California. To stay up to date on the latest about next year's program, sign up for email updates.


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Wednesday, October 20, 2010

Your invitation to attend the CRS Product Development Forum - Poorly Soluble Drugs

CRS Product Development Forum – Poorly Soluble Drugs
January 27-28, 2011
Doral Golf Resort & Spa
Miami, Florida U.S.A.

You are invited to attend an informative two-day program devoted exclusively to the topic of poorly soluble drugs; CRS Product Development Forum – Poorly Soluble Drugs. January 27-28, 2011, Doral Golf Resort & Spa, Miami, Florida.

Who should attend? People from all fields involved in the development of drugs including receptor targets; drug discovery; ADME; pre-formulation (and formulation); human physiology; and in-vitro, in-silico, and in-vivo models and clinical trials (including special populations).

Understanding the Challenges of Poorly Soluble Drugs
Poorly soluble compounds compose an increasingly large percentage of the NCEs being developed today. These substances have great potential, but they present many challenges to effective delivery, including decreased bioavailability and inter-patient variability. Compounding these issues, many of the existing paradigms for drug development do not apply to poorly soluble compounds.

Unlocking the Door to New Paradigms in Drug Delivery
In spite of these challenges, the potential of poorly soluble drugs is too great to be ignored. By developing new formulation strategies, better technologies for enhancing drug solubility, and more efficient methods of delivery, we can extend the life cycle of established low-solubility drugs, increase the number of poorly soluble drug candidates for development, and deliver highly effective and economically efficient treatments to the patient.

This two-day forum will expose those involved in the discrete parts of the process to state-of-the-art information in all areas. With greater understanding of the full spectrum of problems, we can unlock the door to new paradigms in the development and delivery of poorly soluble drugs, to the benefit of patients and the industry. Register now!

This year, the CRS Product Development Forum is co-located with the 15th Annual Drug Delivery Partnerships, January 26-28, 2011, also at Doral. Ask about registration discounts when registering for both meetings.

PROGRAM HIGHLIGHTS

Plenary Topics
Pros & Cons of BSC in Drug Discovery
Formulation Strategies for Delivering Poorly Soluble Actives
Formulation Strategies with Emphasis on Class 4 Compounds—Good Case Stories
Lipolysis Modeling and Food Effect

Session Topics
Human GI Physiology
In-Vivo Studies of Absorption of Poorly Soluble Actives
Solution/Semi-solid Formulation Approaches
In-Vitro Methodologies
Mid- to Late-State Development (Phase II and Beyond)

Click here to view the complete program with confirmed speakers.

CALL FOR PAPERS

October 29, 2010, is the last day to submit your abstract.

REGISTRATION
The registration deadline is January 4, 2011. Register today!


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Thursday, June 3, 2010

Drug Delivery Partnerships 2011 Industry Alert: Official Call For Presenters


From: Jennifer Sobrino, Conference Producer
Re: Call for Speakers & Presentations
Event Date: January 26-28, 2010
Event Venue: Doral Golf Resort & Spa, Miami, FL

SUBMIT YOUR PROPOSAL NOW!

The Institute for International Research (IIR) is currently seeking presenters for the 2011 15th Annual Drug Delivery Partnerships event. This 3-day event will take place January 26-28, 2011 in Miami, FL. We invite you to submit a proposal for a speaking opportunity directly to Jennifer Sobrino, by July 1, 2010. Please send to jsobrino@iirusa.com. Sessions will be 30-45 minutes including Q & A.

Submission Guidelines & Details

CUSTOMIZE YOUR CONFERENCE AGENDA!
We are currently recruiting drug delivery partnership executives who can share NEW DATA through detailed case studies related to leveraging the value of drug delivery to improve product pipelines, patient outcomes and boost innovation. This three day event will focus on current challenges the industry sees today and provide a forum for experts to come together and share knowledge and expertise.

Who will attend the leading industry conference on Drug Delivery Partnerships? Attendees will be both new and experienced drug delivery professionals in business development, technology, assessment & transactions, new product planning & development, R&D and more. We expect that the conference will attract between 400-500 attendees and are looking for novel approaches to handling drug delivery partnership issues including:

• Healthcare reform impact on reimbursement and innovation
• Drug delivery partnerships as a strategy for pipeline value creation
• Regulatory considerations
• Emergence of nanoparticulates as drug carriers
• Drug repurposing
• Innovation for OTC drugs
• Marketplace opportunities for biosimilars
• Regional preference for drug delivery methodologies in emerging markets
• Drug delivery focus in Latin America

MAKE SURE YOUR BIGGEST ISSUES ARE ADDRESSED!

Are your biggest concerns not addressed here? Contact Jennifer Sobrino at jsobrino@iirusa.com or 646.895.7310 to ensure that your pressing issue gets the attention it deserves!

Do you want to reach this audience?

We have a limited number of slots available for solution providers/consultants.
People who wish to become part of the program should contact, Sarah Scarry, Sponsorship Manager, at 646.895.7472 or sscarry@iirusa.com


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Wednesday, June 2, 2010

Q&A on Combination Products

I recently came across this white paper from Issac Medical Companies. It looks at various questions of combination products including:

-How do combination products work, and what advantages do they offer over other methods of drug delivery?
-How has the market arrived at the point where combination products are an important concept for the future of drug delivery?-How versatile are they in their applications?
-What scope is there to increase the range of applications in the future?

Read the white paper here.



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Tuesday, January 26, 2010

Altea and KAI Pharmaceuticals Enter into a Preclinical and Clinical Development Agreement for the Transdermal Delivery of Certain Novel KAI Peptides

ATLANTA, Ga., January 13, 2010. Altea Therapeutics Corporation (“Altea”) announced today that it has entered into a partnership with KAI Pharmaceuticals, Inc. (“KAI”), a drug discovery and development company, for the preclinical and clinical development of certain KAI proprietary peptides utilizing Altea’s proprietary PassPort® Transdermal Delivery System.

Under the terms of the agreement, Altea and KAI will examine the transdermal delivery of certain KAI proprietary compounds using Altea’s novel transdermal delivery technology, the PassPort System. Altea has also granted KAI an option to receive a worldwide technology license for the further development and commercialization of these novel transdermal products. Should KAI exercise the option, KAI will fund all product development, manufacturing and commercialization activities, and Altea may receive license payments, development and commercialization milestones and royalties on product sales from KAI.

“We are pleased to enter into this agreement with KAI Pharmaceuticals, said Dr. Eric Tomlinson, PhD, DSc, President and CEO of Altea Therapeutics. “The agreement further validates the broad application of the Altea Therapeutics novel transdermal patch technology for the transdermal delivery of water-soluble compounds. While we continue to apply our transdermal technology to currently approved drugs that previously were administered by needle injection or infusion, including water-soluble proteins, carbohydrates and small molecules, this new partnership allows us to apply our technology to the new peptide drugs being developed by KAI Pharmaceuticals.”


About Altea Therapeutics

Altea Therapeutics is a privately held clinical-stage pharmaceutical company with a proprietary platform technology broadly applicable to the bolus or sustained transdermal delivery of biological drugs (proteins and carbohydrates) that otherwise would be administered by needle injection or infusion. The Company's PassPort® Transdermal Delivery System also is uniquely suited for delivering highly water-soluble low molecular weight drugs that otherwise could not be delivered transdermally.

Altea Therapeutics has partnered with Amylin Pharmaceuticals, Inc. and Eli Lilly and Company to develop and commercialize a novel daily transdermal patch delivering sustained levels of exenatide (currently marketed as Byetta®). The Company also has a partnership with Hospira, Inc. to develop and commercialize a transdermal patch for delivering enoxaparin sodium (currently marketed as Lovenox®) utilizing the PassPort® Transdermal Delivery System.

Altea Therapeutics is also in clinical development of a Transdermal Basal Insulin Patch for diabetes and a Transdermal Fentanyl Citrate Patch for pain. Additional information about Altea Therapeutics may be found at www.alteatherapeutics.com.

About KAI Pharmaceuticals

KAI is a drug discovery and development company with novel clinical-stage programs in cardiovascular disease, renal complications and pain. KAI’s lead product candidate, KAI-9803, is currently in a Phase 2b study (PROTECTION AMI) designed to assess the effect of KAI-9803 on reducing myocardial injury in heart attack patients. KAI’s second clinical program, KAI-1678, is in Phase 2a studies for pain. KAI’s third program, KAI-4169, is for the treatment of secondary hyperparathyroidism (SHPT) in kidney disease patients and is in IND-enabling studies.

KAI is the leader in the selective modulation of intracellular protein:protein interactions and delivery of peptides into the cell. This approach has broad potential and has been validated clinically. The Company has applied its core expertise to discover highly potent and selective inhibitors and activators for protein kinase C (PKC) isozymes. KAI is based in South San Francisco, California, and can be found online at www.kaipharma.com.

KAI is a registered trademark of KAI Pharmaceuticals.


**************************************************


NOTE: Altea Therapeutics, PassPort, Medicines Made Better. are either registered trademarks or trademarks of Altea Therapeutics Corporation, in the USA and/or other countries. All other brand names, product names or trademarks belong to their respective holders.


The statements in this press release regarding the products of Altea Therapeutics in development, product development plans and projected financial results, are forward-looking statements involving risks and uncertainties that can cause actual results to differ materially from those in such forward-looking statements. Potential risks and uncertainties include, but are not limited to, the ability of Altea Therapeutics to both complete the design, development and manufacturing process development of its products, manufacture and commercialize its products, obtain product and manufacturing approvals from regulatory agencies, manage its growth and expenses, finance its activities and operations, as well as marketplace acceptance of its products.


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Monday, January 25, 2010

DDP 2010: Chairperson’s Welcome and Opening Remarks

Peter Kramer, PhD
Executive Director, Technology Transactions
Bristol-Myers Squibb

Pharma is currently in an unsustainable growth period. The current future is unclear. It’s worth taking the chance in this industry. This industry makes a difference, as AIDS is now a treatable chronic disease. There was also a decrease in cardiovascular disease and survival rates for cancers lasting longer than five years. Kramer is wondering if Pharma is part of the problem or cure? Pharma is an adventure right now, and the 14th Annual DDP is very suited by the magic that Orlando brings. We are all tied together in partnerships. DDP does this for the industry. Collaborative relations and partnerships in drug delivery all make Pharma happen and to be as successful as it is today. With everyone’s participation not only will DDP 14 be a success, but DDP 15 will be even better.


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Monday, September 28, 2009

New Drug Delivery System Uses Magnetism to Release Medication

This article in Cnet highlights an effective new approach to delivering intermittent doses of medication that can not be taken orally. Research led by Daniel Kohane at Children's Hospital Boston has uncovered a tiny implantable device that releases the medication through a membrane by switching on an off a magnetic field.

This is a novel approach to delivering drugs and hopefully we should see this come to hospitals soon. What are some other examples of innovative drug delivery systems that are being researched?

If you'd like to network with other professionals in the drug delivery field, join our LinkedIn group! Or follow our Drug Delivery Twitter here.


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Monday, August 31, 2009

Biologics and RNA Drug Delivery LinkedIn Group Newsletter


Welcome to the August edition of the Biologics and RNA Drug Delivery LinkedIn Group Newsletter. This month, we’re looking at the latest news in the industry and preparing for the Biologics and RNA Drug Delivery Conference in Boston at the end of September! See the bottom of the newsletter for an exclusive discount for you, the LinkedIn Group members.

We have some exclusive video from last year’s Drug Delivery Partnerships event on the future of drug delivery in the pharmaceutical and biotech industry, and the importance of increased pipeline innovation.

Click here to watch it:

http://bit.ly/tu8I1


We invite you to participate in the following discussion question:

What needle-free biological delivery mechanism do you think holds the most promise for improved patient adherence?

http://bit.ly/1a24pS


We also have Twitter! Be sure to follow us for the latest news in drug delivery

http://www.twitter.com/drugdeliveryiir


There are industry breakthroughs in Biologic & RNA drug delivery every day- and we hope that you use this group to keep on top of them! Read on for some of the latest headlines in the drug delivery space:


Protein therapeutics worth $77bn by 2011, says RNCOS

http://bit.ly/dEAkb


Microneedle patch could boost compliance

http://bit.ly/zjPaB



New liquid protein tech could improve drug delivery

http://bit.ly/Sggh6




RXi presents RNA delivery data

http://bit.ly/ES5Lc



Researchers target siRNA delivery

http://bit.ly/vaHWL



We’re gearing up for the Biologics & RNA Drug Delivery event, taking place September 23-25 in Boston, MA. As a member of this LinkedIn group, we’re offering you an exclusive discount of 20% off when you register for the event using the discount code XP1412LINK. To find out more about the conference, download the brochure here:

http://bit.ly/ezMgy


Cheers,

The Biologics Drug Formulation, Development & Delivery Professionals Team

http://bit.ly/4009b5


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