FamiCord AG, Europe's leading cell bank and the third largest worldwide, announced that its CDMO brand Bramble Bio has entered into a manufacturing agreement with Swedish clinical-stage biotechnology company VERIGRAFT AB. The agreement covers the transfer and establishment of the manufacturing process for VERIGRAFT's lead product candidate P-TEV, as well as support for the sourcing and qualification of donated human vein tissue used as starting material. Technology-transfer activities to Bramble Bio's GMP site in Warsaw, Poland, will begin immediately.
The collaboration is expected to run for approximately 18 months and has an estimated contract value in the low single-digit millions of euros, depending on the progress of the clinical program, patient recruitment and associated manufacturing requirements. The agreement supports preparations for the pivotal Phase II/III trial TECVI-2, which is expected to start in Q1 2027. The trial will evaluate P-TEV as a potentially curative treatment for patients suffering from severe chronic venous insufficiency (CVI). Clinical sites are planned in Spain, Poland and the Netherlands, with the trial currently authorized in Spain under the EU Clinical Trials Regulation; approvals in Poland and the Netherlands are expected in Q4 2026.
"The agreement with VERIGRAFT marks another concrete step in the development of our CDMO activities," said Jakub Baran, CEO of FamiCord AG. "Supporting a pivotal Phase II/III program requires close technical cooperation, rigorous process control and reliable cross-border logistics. The project broadens our portfolio with a late-stage clinical program and underlines the capabilities we have built at our Warsaw site."
P-TEV is a personalized, fully biological tissue-engineered vein with a functioning valve. The therapy starts with donated venous tissue, which is decellularized to remove donor cells while preserving the native tissue and valve structure. The resulting matrix is then reconditioned with the patient's own blood to create a personalized graft, designed to replace a diseased vein segment containing a non-functioning valve and restore venous function without requiring immunosuppressive treatment.
"Establishing a robust and scalable manufacturing capability is fundamental to the successful delivery of TECVI-2 and to the future development of P-TEV. Bramble Bio combines specialist ATMP manufacturing expertise with the flexibility and commitment required for a complex, personalized therapy," said Petter Bjorquist, CEO of VERIGRAFT. "We look forward to working closely with their team as we transfer our process and prepare to supply this important multi-country clinical trial."
Simon Boa, Managing Director of Bramble Bio, sees the project as a sweet spot deal for the company. "Technology transfer and clinical manufacturing for a personalized tissue-engineered product require close technical collaboration, rigorous process control and carefully coordinated logistics. These are core areas of expertise for our CDMO team."
Bramble Bio supports biotechnology and pharmaceutical companies with technology transfer, process development and optimization, GMP manufacturing, cellular starting-material sourcing, analytical services and international logistics. In addition to Warsaw, Bramble Bio operates a GMP site in Cantanhede, Portugal. FamiCord, founded in Leipzig in 1997, has expanded its CDMO activities focused on cell and gene therapies, leveraging its established laboratory infrastructure and GMP expertise. Further information on FamiCord can be found at www.famicord.com and on VERIGRAFT at www.verigraft.com.
This agreement matters because it adds a pivotal Phase II/III program to FamiCord's CDMO portfolio, demonstrating the company's ability to support late-stage clinical development of advanced therapies. For VERIGRAFT, securing reliable GMP manufacturing is critical to advancing P-TEV toward marketing authorization applications in Europe and the United States. The collaboration highlights the growing demand for specialized CDMO services in the advanced therapy medicinal products (ATMP) market, which is expected to benefit patients with severe CVI and potentially other underserved conditions.
