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Cyclopharm wins US FDA approval for Technegas

ASX News, Health Care
ASX:CYC      MCAP $157.2M
02 October 2023 15:59 (AEST)
Cyclopharm (ASX:CYC) - Managing Director and CEO, James McBrayer

Source: Cyclopharm

Cyclopharm (ASX:CYC) has received approval from the United States Food and Drug Administration (FDA) to commence commercial sales of its novel drug candidate, Technegas.

Cyclopharm will provide and install Technegas generators in nuclear medicine departments to boost the adoption and use of single-patient consumables.

The approval places CYC in the single largest market for Technegas worldwide, estimated to be worth approximately US$180 million (A$279.8 million) annually for the diagnosis and management of Pulmonary Embolism (PE).

The company plans to kick off the commercial rollout of the drug in early November, after completing the final assembly of its first wave of 200 generators.

“While FDA approval for Technegas is a major milestone for Cyclopharm, our ability to now make this technology available to US clinicians and to the patients they serve, is where the key significance lies,” CYC Managing Director James McBrayer said.

Cyclopharm will implement a planned marketing strategy to maximise sales and operational expertise across 64 countries globally where its product is already approved and established.

To date, the company has received 420 formal expressions of interest in the product from US clinicians and their representative bodies, which have lobbied heavily for Technegas’ approval.

CYC shares were up 5.12 per cent, trading at $2.98 at 3:59 pm AEDT.

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