Daily Newsletter

15 November 2023

Daily Newsletter

15 November 2023

Telix plans $125m acquisition of radiopharmaceuticals company QSAM

Telix with pay $2m upfront, $33m on closing, and up to $90m in milestone-based payments.

Phalguni Deswal November 14 2023

Telix Pharmaceuticals has signed a conditional non-binding term sheet to acquire QSAM Biosciences in a deal worth up to $125m.

The term sheet agreement also includes the acquisition of QSAM’s lead radiopharmaceutical therapeutic agent CycloSam (samarium-153-DOTMP).

Telix will pay $2m in pre-losing collaboration and option fees following signing the term sheet. For the acquisition, the Australian company will also pay $33.1m in equity as ordinary shares, as per a 13 November press release.

QSAM will also be entitled to receive $90m in clinical and commercial milestone-based payments following the closing of the acquisition. The deal is expected to close in Q1 2024, as per a 14 November press release.

If the QSAM acquisition is terminated, the option fee and upfront costs will be converted to QSAM common stock, priced at $6.70 per share.

CycloSam has received an orphan drug designation and rare paediatric disease designation from the US Food and Drug Administration (FDA) for the treatment of paediatric osteosarcoma.

CycloSam is currently being investigated as a potential treatment for primary and metastatic bone cancer, including osteosarcoma. The open-label, unblinded, dose-finding Phase I trial (NCT06008483) for CycloSam is planned for completion in Q1 2024, as per a 16 August press release.

“With CycloSam we plan to leverage Telix's extensive experience and success in distributing short-life radiopharmaceuticals using a cold kit product from a nuclear pharmacy. Given these factors, we see a strong pathway to commercialisation," said Telix managing director and group CEO Dr Christian Behrenbruch in a 13 November press release.

Telix’s pipeline consists of therapeutic and diagnostic radiological agents, including targeted radiation therapy, TLX250 (¹⁷⁷Lu-DOTA-girentuximab). It is currently in Phase I clinical trial (NCT05868174)  as a combination therapy with Merck (MSD)’s M3814 (peposertib) in patients with solid tumours that express carbonic anhydrase IX.

Disease-modifying therapies (DMTs) entering the PD market pose significant opportunities and risks

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. Targeting α-synuclein and other neurotoxic proteins is a key strategy in the late-stage pipeline for DMTs. However, the lack of validated predictive biomarkers of PD progression have made the development of DMTs and neuroprotective agents challenging.

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