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ASCELIA

AN ONCOLOGY-DEDICATED DRUG DEVELOPMENT COMPANY

 
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Regulatory
2025-11-05 | Quarterly Report Q3 2025: Orviglance NDA Submitted to the FDA
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Report
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Regulatory
2025-08-21 | Half-Year Report 2025: Orviglance NDA Submission Approaching
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Report
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Regulatory
2025-05-16 | Quarterly Report Q1 2025: Positive Outcome of Orviglance FDA Meeting in Advance of the NDA Submission
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Report
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Regulatory
2025-04-11 | Annual Report 2024: Orviglance Advances to Registration Phase after Successful Phase 3 Study Completion
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ESEF
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Regulatory
2025-02-07 | Q4 and Full Year Report 2024: Completion of Full Study Report Reinforces Successful Outcomes of SPARKLE Phase 3 Study
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Regulatory
2024-11-07 | Quarterly Report Q3: Successful Outcome from Rights Issue with SEK 105 Million Extends Runway Until Late 2025
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Regulatory
2024-08-15 | Half-Year Report 2024: Orviglance Completes Clinical Development with Successful Phase 3 Study
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Regulatory
2024-05-16 | Quarterly Report Q1: Primary Endpoint Met with Strong Headline Results in Orviglance Phase 3 Study
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Regulatory
2024-04-08 | Annual Report 2023: Solid Progress with Orviglance Phase 3 Patient Recruitment Completed and Headline Results Expected by May 2024
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Report
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Regulatory
2024-02-09 | Q4 and Full Year Report 2023: Strengthened Financial Position Ahead of SPARKLE Phase 3 Study Headline Results in May
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Regulatory
2023-11-08 | QUARTERLY REPORT Q3 2023: Re-evaluation of SPARKLE Phase 3 Study Images Progresses According to Plan
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Regulatory
2023-08-18 | Half-Year report 2023: Re-evaluation required after intra-reader inconsistency in scoring of images from phase 3 study SPARKLE
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Report
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Regulatory
2023-05-11 | QUARTERLY REPORT Q1 2023: Orviglance phase 3 study, SPARKLE, Last Patient Last Visit (LPLV) has been completed
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Report
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Regulatory
2023-04-13 | Correction: Ascelia Pharma publishes annual report for 2022
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Regulatory
2023-04-13 | Ascelia Pharma publishes annual report for 2022
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Regulatory
2023-02-10 | QUARTERLY REPORT Q4 2022: Orviglance phase 3 study, SPARKLE, expected to be completed in Q1 2023.
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Report
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Regulatory
2022-11-04 | QUARTERLY REPORT Q3 2022: Successful completion of two out of three studies for regulatory submission
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Regulatory
2022-08-18 | Half-year report 2022: Strong results from Orviglance Food Effect Study
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About us

Ascelia Pharma is a biotech company focused on orphan oncology treatments. We develop and commercialize novel drugs that address unmet medical needs and have a clear development and market pathway. […]
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Ascelia Pharma AB (publ) (ticker: ACE) today published its half-year financial report for 2022 (January – June 2022), which is now available on the company’s website: https://www.ascelia.com/ir-media/financial-reports/ SIGNIFICANT EVENTS IN Q2 2022Food Effect Study shows strong liver imaging enhancement with Orviglance® both with light meal and fas ...
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Our values

Our values inspire our ambitions, decision making and collaboration to help us reach our highest potential. INTEGRITY We build powerful relationship with mutual respect and adhere to the high ethical […]
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Ascelia Pharma AB
Hyllie Boulevard 34
215 32 Malmö
Sweden
Phone: +46 735 17 91 18

info@ascelia.com

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Ascelia Pharma is a biotech company focused on orphan oncology treatments. We develop and commercialize novel drugs that address unmet medical needs and have a clear development and market pathway. The company has two drug candidates – Orviglance® (former working name Mangoral) and Oncoral – in clinical development.

Ascelia Pharma has global headquarters in Malmö, Sweden, and is listed on Nasdaq Stockholm (ticker: ACE).

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