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FDA OKs Nelarabine Larger Vial Size for T-ALL and T-LBL: Data and Dosing

January 30th 2026

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Cure Today Logo

FDA Approves Larger Nelarabine Vial for Some Leukemias and Lymphomas

January 29th 2026

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Cancer Network Logo

FDA OKs Larger Nelarabine Vial in T-Cell Leukemia and Lymphoma Populations

January 29th 2026

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FDA Clears Larger Vial Size of Nelarabine Injection in T-ALL and T-LBL

January 29th 2026

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Oncology Live Logo

FDA Approves Larger Vial Size for Nelarabine Injection in T-ALL and T-LBL

January 29th 2026

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SH-110 receives FDA orphan drug designation for the treatment of Glioma

July 22nd 2025

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Cure Today Logo

FDA Grants Orphan Status to Liquid Glioma Treatment SH-110

July 18th 2025

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Oncology Live Logo

FDA Grants Orphan Drug Designation to SH-110 for Oral Suspension in Glioma

July 17th 2025July 16th 2025

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AMERICAN PHARMACEUTICAL REVIEW LOGO

Oral Liquid for Brain Cancer Gets FDA Fast Track Designation

July 17th 2025July 16th 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.