AFT Pharmaceuticals (ASX: AFP) has provided a significant update to guidance for the financial year to the end of March 2024 (FY 24).
The update follows a review of January trading and news that Hikma Pharmaceuticals, the US licensee of Maxigesic IV, has made its first sale of the intravenous pain relief medicine, an event that triggers a US$6 million license fee payment to AFT and its development partner Belgium’s Hyloris Pharmaceuticals.
AFT now expects FY 24 operating profit, including the company’s share of the license fee, to range between $23 million to $25 million. AFT’s earlier guidance for an FY 24 operating profit of $22 million to $24 million, excluded the Hikma license income and was subject to finalisation of the US commercialisation plans, and the related investment costs, for Maxigesic Rapid, a prescription-only tablet form of the pain relief medicine approved for sale in the US last year.
The company continues to expect to declare a dividend for FY24.
The new operating profit guidance, which represents an improvement over the $19.7 million operating profit posted in the year to the end of March 2023, follows lower than forecast Australasian sales. This reflected some launch delays and slower than forecast sales offtakes for newly launched products in these markets. It also reflects a decision to take advantage of the Hikma license fee income to accelerate investments for growth. These investments include:
“Trading in Australasia, with some launch delays and slower launch offtakes for new products have represented a headwind to the company. After the license income, these weaker than expected sales represent the largest factor in the change to the operating result,” Managing Director Hartley Atkinson said.
“However, supported by our decades-long record of delivering steady growth in Australasia, we remain confident of our prospects and the value of investing through short term swings.
“Similarly, given our success in international markets we are confident in our ability to take advantage of the strong potential we see for our portfolio of medicines around the world. Given this outlook and the license fee gain, we have resolved it is in shareholders’ interests to continue to significantly invest to support growth.
“In the current financial year, we have struck more than 109 in-licensing agreements1 and expanded our product development portfolio, adding three new projects including a topical treatment for strawberry birthmarks, a treatment for Burning Mouth Syndrome and a treatment for Vulvar Lichen Sclerosus. We also have a further two projects under consideration.