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12-Jun-2023

Bloomsbury Genetic Therapies Completes Successful Scientific Advice Meeting with the MHRA regarding its BGT-NPC Program

- Company intends to move forward with toxicology and biodistribution study in rodents ahead of a single, Phase 1/2/3 trial in Niemann-Pick Disease Type C (NPC) -

London, UK, 12 June 2023 – Bloomsbury Genetic Therapies Limited, a clinical-stage biotechnology company developing potentially curative treatments for patients suffering from rare neurological and metabolic diseases based on clinically proven gene therapy technologies, today announced that a successful scientific advice meeting was held with the UK Medicines and Healthcare products Regulatory Agency (MHRA) on 26 April 2023 confirming the formal toxicology and biodistribution requirements to commence a single, Phase 1/2/3 clinical trial with the Company’s product candidate, BGT-NPC, as a potential new therapeutic for the treatment of NPC. 

The Company met with the MHRA to discuss its preclinical data package and plans. The MHRA confirmed that it was supportive of the Company’s proposal to conduct a single toxicology and biodistribution study in rodents supplemented by published data from precedent intra-brain AAV9 gene therapies, prior to initiating a registrational, Phase 1/2/3 clinical trial for BGT-NPC in the UK. There was no requirement to conduct studies in a larger animal model. Delivering accelerated development is especially important in indications such as NPC, where no curative treatments are currently approved and there is a significant need to improve the standard of care.

The Company is currently completing efficacy studies for BGT-NPC in collaboration with its partner University College London. As a result of the advice and formal feedback received from the MHRA, subject to initiating a manufacturing campaign with its chosen vector Contract Development and Manufacturing Organization (CDMO) partner, the Company intends to initiate a toxicology & biodistribution study in 2024.

“Following our recent, positive regulatory interactions regarding our BGT-DTDS program, this is another success for Bloomsbury’s pragmatic development approach,” said Adrien Lemoine, Co-Founder & Chief Executive Officer of Bloomsbury. “This result confirms our ability to deliver accelerated clinical translation and capital-efficient development by delivering CTA-enabling activities in rodents, as opposed to more expensive and time-consuming studies in non-human primates or larger animals.”

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Last Updated: 12-Jun-2023