Close
Novotech
Jabsco PureFlo 21 Single Use

Spotlight on Abzena’s Developability Platform during Antibody Engineering & Therapeutics 2019

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access the Media Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Related stories

How Mobile Field Hospitals Are Changing Emergency Care

Healthcare systems can collapse overnight, particularly in natural disasters...

How Automation Is Transforming Mail-Order Pharmacy Operations: Efficiency, Accuracy and ROI

This article includes: Expanding the Role of Mail-Order Pharmacies ...

Designing Biotech Financial Models for Series B Success

Building a compelling Series B case in biopharma goes well beyond efficacy data and market size projections. Sophisticated investors are increasingly focused on CMC risk, licensing obligations, and the defensibility of your manufacturing timeline. This article breaks down what the financial model behind a strong Series B actually looks like and what quietly kills deals that should have worked.
- Advertisement -

Abzena is showcasing its new Developability Service, enabling biotechnology and pharmaceutical companies to improve lead selection and de-risk cell line development, at Antibody Engineering & Therapeutics 2019 being held 9–13 December, on Booth #414 at the Marriott Marquis San Diego in San Diego, California.

Building on recent insights from assessing hundreds of drug candidates, Abzena launched its Developability Service in 2019 to help overcome the key challenges of drug design and select lead candidates with the best chances of clinical success. The platform evaluates specificity, functionality, safety and manufacturability of antibodies to reduce the risk, time and expenditure commonly required to progress multiple lead candidates through costly cell line development and manufacturing runs.

Campbell Bunce PhD, Chief Scientific Officer at Abzena, commented: “Developing biotherapeutics typically entails a great deal of risk, cost and time, particularly during later stages of development. Abzena’s Developability Service provides biotechnology and pharmaceutical companies with insights on liabilities and risk factors early in the development process to help identify the next generation of antibodies that stand the best chance of succeeding in the clinic.”

As part of the company’s presence at Antibody Engineering & Therapeutics 2019, Abzena will host a scientific session exploring how developability assessment can limit the risk and expenditure of entering later costly stages of development with multiple lead candidates. Arron Hearn, Group Leader, Protein Engineering at Abzena, will present on “Developability: Evaluating Specificity, Immunogenicity, Functionality, and Manufacturability for Lead Candidate Selection” at 1.15–1.45pm on 10 December.

For more information about Abzena’s Developability Service, please visit Booth #414 at Antibody Engineering & Therapeutics 2019 or https://abzena.com/development-services.

About Abzena
Abzena provides the most complete set of solutions in integrated early discovery to mid-phase biotherapeutic and ADC drug development services in the pharmaceutical industry. The company maintains resources around the world, with facilities in the US and UK. Abzena is partnered with Welsh, Carson, Anderson & Stowe, one of the world’s leading private equity investors. For more information, please see www.abzena.com.

 

Latest stories

Related stories

How Mobile Field Hospitals Are Changing Emergency Care

Healthcare systems can collapse overnight, particularly in natural disasters...

How Automation Is Transforming Mail-Order Pharmacy Operations: Efficiency, Accuracy and ROI

This article includes: Expanding the Role of Mail-Order Pharmacies ...

Designing Biotech Financial Models for Series B Success

Building a compelling Series B case in biopharma goes well beyond efficacy data and market size projections. Sophisticated investors are increasingly focused on CMC risk, licensing obligations, and the defensibility of your manufacturing timeline. This article breaks down what the financial model behind a strong Series B actually looks like and what quietly kills deals that should have worked.

CMC Bottleneck in Drug Development and IND Delays

Ask any experienced biopharma program manager what derails an IND filing most often, and the answer is rarely surprising: it is CMC. Not insufficient efficacy data, not toxicology surprises CMC. This article examines why Chemistry, Manufacturing, and Controls continues to be the most underestimated risk in early drug development, and what program leaders can do about it.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access theMedia Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Translate »