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All MARRegulatory
15 December, 2024
Regulatory

Statement by the Board of Directors of Abliva regarding the public cash offer from Pharming

The Board of Directors unanimously recommends the shareholders to accept the offer.
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9 December, 2024

Abliva Announces Publication of Results from Phase 1a/b Study of KL1333 in the Scientific Journal Brain

-Results demonstrated that KL1333 was safe and well tolerated, with early signs of efficacy in patients with primary mitochondrial disease- Abliva AB (Nasdaq Stockholm: ABLI) a clinical-stage company ...
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29 November, 20249 December, 2024
Regulatory

Abliva AB Interim Report January – September 2024

- Positive Interim Analysis of the FALCON Study Paves the Way for KL1333 Development -
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16 September, 20249 December, 2024

Join Abliva for World Mitochondrial Disease Week 2024, September 16 – 22

-The company shares videos each day of the week to raise awareness about mitochondrial disease and to highlight ongoing activities at Abliva- Abliva AB (Nasdaq Stockholm: ABLI), a clinical-stage compa ...
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30 August, 20249 December, 2024
Regulatory

Amended number of shares and votes in Abliva AB (publ)

Abliva AB (Nasdaq Stockholm: ABLI) today announces that the number of shares and votes in the Company has increased by 262,500,000, as a result of the conversion of a convertible loan announced by the ...
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22 August, 20249 December, 2024
Regulatory

Abliva AB Interim Report January – June 2024

FALCON Positioned for Success Following Analysis by Independent Committee ⎮ Strong Safety Profile Confirmed, and Both Primary Endpoints Passed Futility
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19 July, 2024
Regulatory

Positive interim analysis in Abliva’s FALCON study triggers convertible loan conversion

Abliva AB (Nasdaq Stockholm: ABLI) a clinical-stage company developing medicines for the treatment of rare and severe primary mitochondrial disease, today announced that the convertible loan of SEK 42 ...
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18 July, 2024
Regulatory

Abliva Announces Positive Interim Analysis of the FALCON Study for KL1333 in Primary Mitochondrial Disease

-Independent committee confirms FALCON study is powered for potential success with both alternative endpoints passing futility- -Committee confirms strong safety profile of KL1333- -Abliva to hos ...
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31 May, 2024
Regulatory

Amended number of shares and votes in Abliva AB (publ)

Abliva AB (Nasdaq Stockholm: ABLI) today announces that the number of shares and votes in the Company has increased by 103,149,954, as a result of a preferential rights issue announced by the Board of ...
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30 May, 2024

Abliva Announces Completion of 24 Weeks of Dosing in Wave 1 of the FALCON Study of KL1333 in Primary Mitochondrial Disease

-With 24 weeks of dosing complete, Abliva remains on track to report the interim analysis in early Q3 2024- Abliva AB (Nasdaq Stockholm: ABLI) a clinical-stage company developing medicines for [&helli ...
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23 May, 2024
Regulatory

Resolutions from Annual General Meeting in Abliva AB (publ) on May 23, 2024

Abliva AB (Nasdaq Stockholm: ABLI) (”Abliva” or the ”Company”) today on May 23, 2024, held its Annual General Meeting (“AGM”). A summary of the resolution follows.
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23 May, 2024
Regulatory

Abliva AB Interim Report January – March 2024

SEK 46 million raised through preferential rights issue | Preparations for the interim analysis ongoing
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This is Abliva

  • Delivering mitochondrial health
  • Orphan Drugs
  • Relevant publications

Research & Development

  • Research & Development
  • KL1333
  • NV354
  • Early programs
  • The FALCON Study

Contact

Abliva AB, member of Pharming Group
Medicon Village
223 81 Lund, Sweden

Phone
+31 (0)71 5247 400

Generel questions
info@pharming.com

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