CiMaas BV, a company developing cellular immunotherapy for cancer, and PharmaCell BV, a contract manufacturing organization for cellular therapies and regenerative medicine in Europe, have agreed to collaborate on the clinical development of CiMaas’ products.
 
PharmaCell will provide consulting services on writing GMP-compliant documents for the purpose of translating the CiMaas cell therapy processes into GMP. Options have been taken on a full technology transfer to be executed at a later date, along with an option on a Phase I and Phase II trial.
 
Gerard Bos, chief executive officer of CiMaas said, “We are delighted to collaborate with PharmaCell and receive support in building our documents and technology in a fully GMP compliant manner for the development of our ATMPs (Advanced Therapy Medicinal Products).”
 
Wilfred Germeraad, chief scientific officer added, “It is a wonderful opportunity to work together and it will immediately speed-up our work in translating the lab procedures into clinical products ready to be tested in patients with cancer.”
 
Alexander Vos, chief executive officer of PharmaCell BV, said, “The CiMaas team has shown to be successful in bringing their technology to the point of preparing the initiation of clinical studies. We are excited to support them to make their production process GMP-compliant and help clear the path to bring their innovative therapies to benefit patients.”