Leqselvi (Deuruxolitinib) | Severe Alopecia Areata | DengYue

  • Generic Name/Brand Name: ​Deuruxolitinib phosphate / Leqselvi
  • Indications: Adults with severe alopecia areata
  • Dosage Form: ​Oral tablets
  • Specification: 8 mg per tablet

Deuruxolitinib Application Scope

deuruxolitinib
deuruxolitinib

 

Leqselvi is approved for the treatment of severe alopecia areata in adults.

 

Deuruxolitinib Characteristics

  • Ingredients:

    • Active: Deuruxolitinib phosphate

    • Inactive: Colloidal silicon dioxide, lactose monohydrate, low-substituted hydroxypropyl cellulose, magnesium stearate, microcrystalline cellulose, povidone; film coat contains carmine, FD&C Blue #2 aluminum lake, glyceryl mono and dicaprylocaprate, polyvinyl alcohol, sodium lauryl sulfate, talc, titanium dioxide

  • Properties:​ Janus kinase (JAK) 1 and 2 inhibitor

  • Packaging Specification:​ 8mg tablets, supplied in bottles with a child-resistant cap

  • Storage: Store at room temperature between 68°F to 77°F (20°C to 25°C); protect from moisture

  • Expiry Date: ​Refer to the packaging for the specific expiration date

  • Executive Standard: ​FDA-approved labeling

  • Approval Number: NDA 217900

  • Date of Revision: ​July 2024

  • Manufacturer: Manufactured for Sun Pharmaceutical Industries, Inc. by Halo Pharmaceutical Inc., Whippany, NJ, USA

Guidelines for the Use of Deuruxolitinib

  • Dosage and Administration:

    • Recommended dosage is 8 mg orally twice daily, with or without food

    • If a dose is missed, skip the missed dose and resume at the next scheduled time

  • Adverse Reactions:

    • Common (≥1%): Headache, acne, nasopharyngitis, increased blood creatine phosphokinase, hyperlipidemia, fatigue, weight gain, lymphopenia, thrombocytosis, anemia, skin and soft tissue infections, neutropenia, herpes

  • Contraindications:

    • Patients who are CYP2C9 poor metabolizers

    • Concurrent use with moderate or strong CYP2C9 inhibitors

  • Precautions:

    • Increased risk of serious infections, including tuberculosis; screen for latent TB before initiating therapy

    • Higher rates of malignancies and major adverse cardiovascular events (MACE) have been observed with JAK inhibitors

    • Monitor for gastrointestinal perforations, laboratory abnormalities (e.g., anemia, neutropenia), and lipid elevations

    • Avoid use of live vaccines during or immediately prior to treatment

Deuruxolitinib Interactions

  • Drug Interactions:​
  • Avoid concomitant use with strong CYP3A and moderate or strong CYP2C9 inducers, as they may decrease deuruxolitinib efficacy

  • Contraindicated with moderate or strong CYP2C9 inhibitors due to increased risk of adverse reactions

 

Note:

  • If there is a new packaging for the drug, the new packaging shall prevail. The above information is sourced from DengYue Medicine.
  • It is only for internal discussion among medical staff and does not serve as a basis for medication. For specific medication guidelines, please consult the attending physician.
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