spacer
home > news > detailed info
INDUSTRY NEWS AND PRESS RELEASES

3P Biopharmaceuticals enters into manufacturing agreement with the Swedish company Affibody

3P Biopharmaceuticals

The arrangement covers process transfer, process development and GMP manufacture of Affibody’s candidate

[Noáin, May 27, 2019] 3P Biopharmaceuticals, a leading CDMO specialized in the process development and GMP manufacturing of biologics, has signed a collaboration agreement with the Swedish company Affibody for the process transfer, scale-up and GMP commercial manufacturing of a recombinant protein sole property of Affibody.

According to the agreement, 3P is responsible for transferring and scaling up the process developed by Affibody prior to execution of the first GMP manufacturing batches. 3P will also perform the process characterization and validation before entering the commercial batch manufacturing stage.

“We are very pleased to be working with Affibody on this project and to create a strong long-term partnership with them. We are sure that this is a mutually beneficial agreement” says Dámaso Molero, General Manager at 3P Biopharmaceuticals.
Besides, “ensuring large scale high quality production of our ABY-035 drug is a natural next step in our evolution as a company with the ambition to have development, manufacturing, and commercialization expertise”, explained David Bejker, CEO of Affibody who added that “the work we have initiated together with 3P is important for us and we look forward to working with 3P.”

This collaboration validates the experience and know-how of 3P’s microbial services in the production of recombinant proteins. Thus, 3P, as a global manufacturing partner, has proven experience in both clinical and commercial production in E.coli included process validation and process characterization.

FOR MORE GRAPHIC MATERIAL CLICK HERE.

About Affibody

Affibody is a private clinical-stage Swedish biotech company focused on developing into an integrated biopharma company utilizing next generation biotherapeutics based on its unique proprietary technology platforms: Affibody® molecules and Albumod™. The company operates a focused experimental medicine model and currently has three clinical-stage programs. The first two are therapeutic programs that target psoriasis and rare Immunoglobulin G (IgG)-mediated autoimmune diseases. The third program is a diagnostic imaging program that is directed primarily towards metastatic breast cancer. In addition to its portfolio of innovative drug projects, the company offers the half-life extension technology, Albumod™, for outlicensing.

Further information can be found at: www.affibody.com

About 3P Biopharmaceuticals
 
3P Biopharmaceuticals is a leading CDMO specialized in the process development and GMP manufacturing of biologics and cell therapy products. 3P offers solutions for all stages of biologics development: process as well as analytics development, preclinical and clinical material supply, commercial production. 3P is well known for its extensive experience, flexibility and team of professionals.
3P has the support of an important group of investors: Cinfa Group. Cinfa Group is a holding of companies that handles different business lines in the world of health, with more than 50 years of experience and expertise in the biotech and pharma market. It's flagship company, Laboratorios Cinfa, is a successful manufacturer that ranks first in terms of generics´ retail in Spanish pharmacies.

For further information: http://www.3pbio.com/

3P Biopharmaceuticals press contact:

Isabel García
Communications and Marketing Responsible at 3P Biopharmaceuticals
Tlf: + 34 948 346 480
email: igarcia@3pbio.com
phone +34 948 34 64 80
email info@3pbio.com
web www.3pbio.com
email Polígono Mocholí, C/ Mocholí 2, 31110 Noáin, Navarra, Spain
 
Print this page
Send to a friend
   
spacer
News and Press Releases

Destiny Pharma appoints MedPharm to develop new XF-platform drug formulations

Destiny Pharma, a clinical stage biotechnology company focused on the development of novel antimicrobial drugs, is pleased to announce that it has appointed MedPharm as its expert partner to develop new topical formulations of the Company’s novel XF-platform compounds. These new treatments for dermal and ocular infections are part of its second clinical programme to address the global problem of anti-microbial resistance (AMR). MedPharm is a world leading contract provider of topical and transdermal product design and formulation development services using sophisticated in vitro models to de-risk development programmes.
More info >>


White Papers

Tightening Your Supply Chain Against Counterfeits

World Courier

As today’s global pharmaceutical supply chain grows increasingly longer and more complex, each link provides added opportunity for counterfeiters. While pending regulatory changes promise to tighten the supply chain with respect to production and distribution entities and new packaging technologies will make the identification of counterfeit products easier, the logistics of global distribution remains a weak link. How can the pharmaceutical shipper ensure the security of the supply chain over thousands of miles and extended periods of time when the product is no longer in his possession?
More info >>

Industry Events

DIA 2019 Global Annual Meeting

23-27 June 2019, San Diego Convention Center

DIA 2019 is more than just a meeting: it’s where brilliant minds come together to create solutions. Thousands of global innovators will convene to engage in discussions on today’s hottest topics in the life sciences field, propose ways to combat daily challenges, and network to create lasting connections.
More info >>

 
©2000-2011 Samedan Ltd.
Add to favourites

Print this page

Send to a friend
Privacy statement