Zepuping (Gecacitinib) – Myelofibrosis | HongKong DengYue Medicine

  • Generic Name/Brand Name: ​Gecacitinib / Zepuping®
  • Indications: Myelofibrosis
  • Dosage Form: ​Capsules
  • Specification: 50 mg × 60 capsules/bottle

Gecacitinib Application Scope

Gecacitinib is a dual JAK/ACVR1 inhibitor indicated for the treatment of adult patients with intermediate-2 or high-risk primary or secondary myelofibrosis (MF), including those with anemia. It has demonstrated efficacy in reducing spleen volume, alleviating symptoms, and improving anemia in clinical trials.

zepuping gecacitinib
zepuping gecacitinib

Gecacitinib Characteristics

  • Ingredients: Gecacitinib hydrochloride (active ingredient)

  • Properties:​ Oral solid dosage form; capsules

  • Packaging Specification:​ 50 mg × 60 capsules/bottle

  • Storage:​ Store in a cool, dry place; protect from light

  • Expiry Date: 24 months from the date of manufacture

  • Executive Standard: ​Conforms to national drug quality standards

  • Approval Number: H20250023 (example format; refer to local label for specific country code)

  • Date of Revision: Refer to most recent local prescribing information

  • Manufacturer: Suzhou Zelgen Biopharmaceuticals Co., Ltd.

Guidelines for the Use of Zepuping

  • Dosage and Administration:

    • Recommended Dose: 100 mg orally once daily

    • Administration: Take with or without food; swallow whole; do not chew or crush

    • Missed Dose:​ If a dose is missed, take it as soon as remembered unless it is almost time for the next dose; do not double the dose to make up for a missed dose

  • Adverse Reactions:

    • Common Adverse Reactions: Anemia, thrombocytopenia, neutropenia, leukopenia, diarrhea, nausea, fatigue

    • Serious Adverse Reactions: Severe infections, gastrointestinal perforation, thrombosis, hemorrhage

  • Contraindications:

    • Hypersensitivity: Known hypersensitivity to gecacitinib or any excipient

    • Pregnancy: Contraindicated during pregnancy; may cause fetal harm

    • Lactation: Not recommended during breastfeeding

  • Precautions:

    • Hematologic Monitoring: Regular monitoring of complete blood counts is recommended

    • Infection Risk: Monitor for signs of infection; appropriate antimicrobial therapy should be initiated if an infection occurs

    • Liver Function: Monitor liver function tests periodically

    • Gastrointestinal Perforation: Monitor for signs and symptoms of gastrointestinal perforation

    • Thrombosis: Monitor for signs and symptoms of thrombosis

Gecacitinib Interactions

  • CYP3A4 inhibitors (e.g., ketoconazole, itraconazole) – may increase Gecacitinib plasma levels → monitor for toxicity

  • CYP3A4 inducers (e.g., rifampin, carbamazepine) – may reduce efficacy → avoid or adjust dose

  • Other myelosuppressive agents – additive hematologic toxicity → monitor CBC

  • Anticoagulants / Antiplatelets – increased bleeding risk → monitor clinically

  • Strong P-gp inhibitors – may increase absorption → monitor for adverse effects

 

Note:

  • If there is a new packaging for the drug, the new packaging shall prevail. The above information is sourced from DengYue Medicine.
  •  This content is for reference only. Prescription drugs must be used under a doctor’s guidance and purchased from authorized sources.
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