Wrap-Up from Interview with Deputy CEO Julie Waras Brogren
We recently hosted an event in conjunction with the Q3 report and the announcement of the full data package completion for the Phase 3 Orviglance – SPARKLE study.
As Ascelia Pharma prepare for the pre-submission meeting with the FDA and the planned NDA filing for Orviglance in mid-2025, investors should anticipate an increase in costs. To support this, the company conducted a fully subscribed rights issue in Q3, raising SEK 105 million gross. Additionally, further funding is expected from the TO1 warrant in April 2025, which, if fully subscribed, could bring in another SEK 70 million. Beyond funding efforts, Ascelia Pharma is in active discussions with potential partners for the full commercialization of Orviglance. Terms have not yet been announced but are expected to include milestone payments and royalties.
Orviglance addresses an unmet need in liver imaging for cancer patients with severe kidney impairment, a market valued at approximately USD 800 million, with half of the potential in the U.S.
Deputy CEO Julie W. Brogren shared two highly insightful slides, presenting the primary and secondary endpoints from the full study report.
Primary endpoint:
Secondary endpoint:
With strong data on both primary and secondary endpoints, a robust balance sheet, and promising partnership discussions, Ascelia Pharma is well-positioned to achieve its milestone objectives.
Listen to the interview here: Ascelia Pharma interview
Disclaimer: HC Andersen Capital receives payment from the Ascelia Pharma for a Digital IR/Corporate Visibility subscription agreement. Analyst Claus Thestrup 8:15 AM, 14.11.2024
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Ascelia Pharma
Ascelia Pharma är ett läkemedelsbolag. Bolaget är specialiserat på utveckling av särläkemedel inom onkologi (cancer). Bolaget utvecklar diverse läkemedelskandidater, där störst användning återfinns inom behandling av cancer som drabbat lever och magsäck. Bolaget grundades år 2000 och har huvudkontor i Malmö, Sverige, men är verksamt på en global marknad.
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