Daily Newsletter

23 November 2023

Daily Newsletter

23 November 2023

Syncona to acquire biotechnology company Freeline Therapeutics

Freeline is focused on the development of innovative gene therapies for chronic debilitating diseases.

RanjithKumar Dharma November 23 2023

Syncona’s newly established portfolio company has signed a definitive agreement to acquire clinical-stage biotechnology company Freeline Therapeutics Holdings in an all-cash transaction.

The portfolio company will acquire all Freeline shares not currently owned by Syncona for $6.50 per American depositary share.

Freeline's total issued share capital is therefore valued at $28.3m, a 51% premium compared to the closing price before Syncona's initial proposal announcement on 18 October 2023.

Freeline is focused on the development of innovative gene therapies for chronic debilitating diseases.

The company leverages its rationally designed AAV vector and capsid, AAVS3, and new promoters and transgenes to deliver a functional copy of a therapeutic gene into human liver cells.

It is currently advancing FLT201 gene therapy [a highly differentiated candidate] in a Phase I/II clinical trial in individuals with Gaucher disease type one. This therapy delivers a new transgene.

Freeline has other research programmes, including one focused on GBA1 [glycosylceramide beta 1]-linked Parkinson's disease, which utilises the same new transgene as FLT201.

Freeline CEO Michael Parini stated: “Given the compelling data that we have seen from the first two patients treated with FLT201, we are committed to advancing FLT201 as expeditiously as possible, and we believe we will be better positioned to do that as a privately held, Syncona-backed company than we could by continuing as a publicly traded company in the current environment.”

Subject to the approval of Freeline’s minority shareholders, the deal is anticipated to be completed in the first quarter of 2024.

Syncona will offer Freeline secured convertible debt financing of up to $15m.

This funding will support operations and the ongoing development of FLT201 until the transaction is finalised.

Acute Renal Failure (ARF) - Market Landscape

Only a handful of approved therapeutic drugs are currently available for the treatment of ARF, all belonging to the solute carrier family 12 member 1 inhibitor. The clinical trial space in ARF consists of almost an equal mix of commercial as well as academic sponsors, with Iran and the US emerging as the key countries for conducting Phase III trials. While the current marketed drug space for ARF has only a handful of treatment options, currently available mid-to-late-stage pipeline drugs are likely to pave the way for a new treatment approach in the future.

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