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Shorla Oncology: A Leader in Innovative Oncology Solutions
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FDA Approves Nelarabine Injection for T-cell Leukemia and Lymphoma

July 18th 2025March 27th 2023

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US FDA approves Shorla’s oncology drug for T-cell leukaemia

March 20th 2023

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Shorla wins FDA approval for leukaemia drug

March 20th 2023

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Irish-founded Shorla Oncology secures FDA approval for leukaemia drug

March 9th 2023

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Improve Oncology Drug Shortages with A More Reliable Supply Source

October 13th 2022October 10th 2022

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Our CEO on Biocentury’s Bio€quity Europe podcast

May 25th 2022May 18th 2022

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3 Keys To A Successful Biotech Launch

February 28th 2022February 1st 2022

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Shorla: making women’s and children’s cancer drugs more accessible

March 7th 2022December 22nd 2021

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PharmaVoice Women of the Week – Podcast

March 7th 2022June 2nd 2021

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IRELAND HQ:
Questum Acceleration Center,
Ballingarrane Science & Technology Park,
Clonmel, Co. Tipperary,
E91 V329, Ireland

Shorla Pharma Ltd trading as Shorla Oncology®

All trademarks are the property of their respective owners.

US OFFICE:
245 Main St.,
2nd floor,
Cambridge,
MA 02142, USA

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©SHORLA ONCOLOGY® 2025

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  • About Us
    • Executive Team
    • Leadership Team
    • Board of Directors
    • Advisory Team
  • Products
    • TEPYLUTE
    • IMKELDI
    • JYLAMVO
    • Nelarabine Injection
  • Pipeline
  • News
    • Company Updates
    • Media
  • Careers
  • Contact

Now approved for use in Pediatrics

  • Treatment of pediatric patients with polyarticular juvenile idiopathic arthritis (pJIA).
  • Treatment of pediatric patients with acute lymphoblastic leukemia (ALL) as part of a combination chemotherapy maintenance regimen.

Please click here for the full Prescribing information, including Boxed Warning regarding embryo-fetal toxicity, hypersensitivity reactions, and severe adverse reactions.