Close
Almac
Achema middle east

Lonza and Junshi Biosciences Collaborate to Accelerate the Development and Manufacturing of Biologics

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

First GLP-1 Pill for Obesity by Novo Nordisk Approved by FDA

The U.S. Food and Drug Administration – FDA on...

How High-Achievers Stay Future-Ready in Evolving Job Markets

Job markets today are transforming rapidly. In the past...

Proactive Risk Management as a Core Capability in Pharma Development

Risk management in pharma is often treated as a reactive compliance box-ticking exercise. This article argues for reframing risk as a strategic competitive advantage. It details proactive frameworks like the "Excipient Exclusion Filter," Decision Quality (DQ) matrices, and "pre-mortem" analyses that allow development teams to anticipate failure modes and engineer them out of the pipeline before they occur.
- Advertisement -

“The signing of this collaboration indicates that the relationship between the two parties has been taken to a new level. As a major milestone for Lonza’s biopharmaceutical facility in Guangzhou, the collaboration also demonstrates Lonza’s vision to provide high-quality and reliable services for local pharmaceutical companies under the CDMO model. We look forward to providing comprehensive services and professional support for Junshi Biosciences, helping to accelerate the process of drug development, production and commercialization.”

Quote from Dr. Hui Feng, Chief Operating Officer of Junshi Biosciences:

“We are excited to expand our collaboration with Lonza and believe that, by leveraging our rich global experience and strong local expertise, we will be well placed to achieve the best results. In the future, we believe that supported by Lonza’s advanced technologies and excellent international service, Junshi Biosciences will be able to provide patients with treatment options that work better and cost less in China and around the world, providing an opportunity for patients globally to benefit from China’s innovation capabilities.”

Shanghai, China, 13 April 2021 – Lonza, a leading global contract development and manufacturing organization (CDMO), and Junshi Biosciences, an innovative Chinese pharmaceutical company, today announced that the companies have expanded their collaboration for the development and manufacturing of biologics. Lonza will leverage its global network and local operation capabilities to help Junshi Biosciences accelerate the development of drugs in its pipeline and promote their adoption across global markets.

Under the terms of the agreement, Lonza will provide comprehensive support, including cell line construction and development, the supply of cell culture media and reagents, process development, and GMP manufacturing. The collaboration will also extend to development and manufacturing support for Junshi Biosciences’ current and future antibody-based product pipeline. The pipeline includes a new antibody candidate that will be manufactured at Lonza’s first mammalian facility in Guangzhou (CN) that has been fully operational since Q1 2021.

The main production platform will utilize Lonza’s GS Xceed® Expression System, which is highly recognized in the industry and covers various techniques and commercialized processes such as host cells, expression vectors and optimized culture media. In addition, Lonza will leverage its manufacturing network for biological products spanning three continents as well as its globally unified quality control standards to help Junshi Biosciences accelerate its venture into international markets and help bring innovation from China to the world.

With the help of Lonza’s GS Xceed® Expression System, Junshi Biosciences already successfully launched China’s first local antibody targeting PD-1 (Toripalimab Injection, TUOYI®) in 2018 and took its neutralizing antibody drug JS016 (etesevimab) for COVID-19 to clinical trial stage in 2020.

Latest stories

Related stories

First GLP-1 Pill for Obesity by Novo Nordisk Approved by FDA

The U.S. Food and Drug Administration – FDA on...

How High-Achievers Stay Future-Ready in Evolving Job Markets

Job markets today are transforming rapidly. In the past...

Proactive Risk Management as a Core Capability in Pharma Development

Risk management in pharma is often treated as a reactive compliance box-ticking exercise. This article argues for reframing risk as a strategic competitive advantage. It details proactive frameworks like the "Excipient Exclusion Filter," Decision Quality (DQ) matrices, and "pre-mortem" analyses that allow development teams to anticipate failure modes and engineer them out of the pipeline before they occur.

Rethinking Pipeline Value Beyond Peak Sales Forecasts

The traditional reliance on risk-adjusted Net Present Value (rNPV) and peak sales forecasts is failing to capture the true potential of modern pharmaceutical assets, particularly platform technologies. This article introduces holistic valuation frameworks like Real Options Analysis (ROA) and the Platform VISTA model, arguing for a shift toward valuing "strategic fit," "lifecycle potential," and the intangible equity of innovation engines.

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 »