Arcturus Therapeutics Gains Momentum with Regulatory Approval and Clinical Advancements
• Arcturus Therapeutics' Kostaive vaccine receives Japanese regulatory approval for updated JN.1 formulation, expected to generate $85 million in revenue. • The company's cystic fibrosis treatment, ARCT-032, advances to Phase 2 study after promising Phase 1/1b trial results. • Arcturus is awaiting European Medicines Agency (EMA) decision on Kostaive approval, anticipated in the third quarter of 2024.
Arcturus Therapeutics (NASDAQ: ARCT) is experiencing positive momentum with recent regulatory achievements and advancements in its clinical programs. The Japanese Ministry of Health, Labor and Welfare has approved the updated JN.1 formulation of Arcturus' Kostaive vaccine for adults 18 and over, marking an anticipated annual update for the new strain of the vaccine. This endorsement follows the initial approval of Kostaive in Japan in November 2023.
In collaboration with partners CSL and Meiji, Arcturus Therapeutics is preparing to distribute approximately 4 to 4.5 million doses of Kostaive in October. This distribution is projected to generate around $85 million in revenue for Arcturus. However, the exact timing of revenue recognition remains uncertain and is not expected until 2025 due to profit-sharing intricacies with its partners. The company is also scheduled to present further antibody persistence data at the upcoming XII Options Conference in Brisbane, Australia, from September 29 to October 2.
Arcturus is also awaiting a decision from the European Medicines Agency (EMA) regarding the approval of Kostaive, which is anticipated in the third quarter of 2024. A positive decision from the EMA would further expand the global reach of Arcturus' COVID-19 vaccine.
In addition to its vaccine program, Arcturus Therapeutics is making significant strides in its clinical trials for ARCT-032, a treatment for cystic fibrosis. The U.S. Food and Drug Administration (FDA) has granted approval for the company to commence a Phase 2 study, following promising results from Phase 1/1b trials that demonstrated early efficacy and a positive safety profile. Investment firms Canaccord Genuity and William Blair have maintained positive ratings on Arcturus, expressing confidence in the company's cystic fibrosis program. The Cystic Fibrosis Foundation's Therapeutics Development Network is also backing this program, reflecting heightened patient interest.
Arcturus Therapeutics reported a Q2 2024 revenue of $49.9 million, despite a net loss of $17.2 million. The company maintains a robust cash position of $317.2 million, ensuring financial stability through Q1 2027. These financial results reflect progress across the company's vaccine and therapeutic franchises, including the anticipated launch of Kostaive in Japan.
Arcturus Therapeutics holds a market capitalization of approximately $557.34 million. Despite the recent Japanese regulatory approval, Arcturus has faced challenges, as evidenced by a negative gross profit margin of -18.43% over the last twelve months as of Q2 2024. The company's stock price has experienced significant volatility, with a 6-month total price return of -42.85%. Arcturus maintains more cash than debt, providing financial flexibility in the near term. However, analysts have revised earnings downwards for the upcoming period, and the company is not expected to be profitable this year.

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Canaccord highlights Arcturus stock potential amid regulatory wins - Investing.com
investing.com · Sep 17, 2024
Canaccord Genuity maintains Buy rating on Arcturus Therapeutics, following Japanese approval of Kostaive JN.1. Arcturus ...