Daily Newsletter

11 October 2023

Daily Newsletter

11 October 2023

Cellipont and Diakonos to develop cell therapy for glioblastoma

The US Food and Drug Administration granted fast-track designation for the DOC1021 vaccine.

Vishnu Priyan October 11 2023

Cellipont Bioservices has signed an agreement with Diakonos Oncology for the development of DOC1021, a cell therapy to treat glioblastoma multiforme (GBM).

The parties will carry out the process development and current good manufacturing practice (cGMP) production of DOC1021 for GBM and other cancers.

Diakonos CEO Mike Wicks stated: “As DOC1021 is personalised to each patient, it was critical to find a CDMO [contract development and manufacturing organisation] partner that could not only help commercialise this incredibly promising treatment but exceed our quality standards for each and every patient. 

“We could not be happier to find that partner in Cellipont, and we look forward to changing patient outcomes in GBM as well as other cancer indications.”

An autologous dendritic cell vaccine, DOC1021 stimulates a natural anti-viral immune response against tumours. 

Based on the promising safety and efficacy data from a Phase I clinical trial, the US Food and Drug Administration granted fast-track designation for the vaccine.

Cellipont Bioservices board chairman Darren Head stated: “We are deeply honoured to have been chosen as Diakonos’ partner in this critical endeavour. 

“With our extensive expertise in cell therapy development and manufacturing, coupled with our purpose-built Woodlands facility, we are confident that our collaboration will pave the way for bringing this life-saving therapy to countless glioblastoma patients.”

In March 2023, Cellipont received a debt facility investment from healthcare investment company OrbiMed to conclude works at a cell therapy and gene-modified cell therapy manufacturing facility in the Woodlands, Texas.

Cell & Gene Therapy coverage on Pharmaceutical Technology is supported by Cytiva.

Editorial content is independently produced and follows the highest standards of journalistic integrity. Topic sponsors are not involved in the creation of editorial content.

Significant opportunities and risks for disease-modifying therapies (DMTs) entering the PD market

As PD therapy currently centers on symptomatic treatment, the need for DMTs is one of the greatest unmet needs. Several companies within the late-stage PD pipeline are developing drugs that target PD via novel MOAs. KOLs remain hopeful that these companies will uncover a class of drugs that works effectively to slow or modify the disease course. Targeting α-synuclein and other neurotoxic proteins is a key strategy in the late-stage pipeline for DMTs.

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