Partruvix (Pamiparib) – gBRCA | HongKong DengYue Medicine

  • Generic Name/Brand Name: ​Pamiparib/Partruvix
  • Indications:Germline BRCA mutation-associated recurrent advanced ovarian, fallopian tube, and primary peritoneal cancer
  • Dosage Form: ​Administered orally in the form of capsules
  • Specification: 20 mg/capsule x 60 capsules / bottle

Pamiparib Application Scope

It is approved in China for the treatment of germline BRCA mutation-associated recurrent advanced ovarian, fallopian tube, or primary peritoneal cancer in patients who have previously undergone two or more lines of chemotherapy.

partruvix pamiparib
partruvix pamiparib

Pamiparib Characteristics

  • Ingredients: Pamiparib

  • Properties:​ The capsule shell is opaque. The contents are yellow pellets

  • Packaging Specification: Available Strength: 20 mg/capsule (calculated as C₁₆H₁₅FN₄O); Package Size: 60 capsules per bottle/box

  • Storage:​ Store at room temperature (details not explicitly found in sources; general recommendation is 20-25°C)

  • Expiry Date: To be stated on the specific packaging based on the manufacturing date, typically 24-36 months

  • Executive Standard: Complies with the quality standards approved by the National Medical Products Administration (NMPA) of China

  • Approval Number: Approved by the National Medical Products Administration (NMPA) in China

  • Date of Revision: Approved by the National Medical Products Administration (NMPA) in China

  • Manufacturer: BeiGene Ltd

Guidelines for the Use of Pamiparib

  • Dosage and Administration:

    • Recommended Dose: 40 mg taken orally twice daily.

    • Administration: Swallow capsules whole with or without food.

    • 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 doses.

  • Adverse Reactions:

    • Common Adverse Reactions:

      • Blood and lymphatic system disorders: Anemia, leukopenia, neutropenia, thrombocytopenia, lymphocytopenia.

      • Gastrointestinal disorders: Nausea, vomiting, diarrhea, abdominal pain, decreased appetite.

      • General disorders and administration site conditions: Fatigue.

      • Investigations: Increased AST, increased ALT, increased blood bilirubin.

    • Serious Adverse Reactions:

      • Myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) have been reported with PARP inhibitors.

      • Severe hematological toxicities (e.g., severe anemia, neutropenia, thrombocytopenia).

      • If serious adverse reactions occur, dose interruption, reduction, or discontinuation may be necessary.

  • Contraindications: Hypersensitivity to pamiparib or any component of the formulation.

  • Precautions:

    • Use with caution in patients with hepatic or renal impairment.

    • Not recommended during pregnancy or breastfeeding.

    • Effective contraception is advised for women of childbearing potential during and after treatment.

Pamiparib Interactions

  • CYP3A Inhibitors: Co-administration may increase pamiparib levels, potentially enhancing side effects.

  • CYP3A Inducers: Co-administration may decrease pamiparib efficacy.

  • Other Chemotherapeutic Agents: Concurrent use may exacerbate hematological toxicities.

  • Anticoagulants and NSAIDs: Increased bleeding risk due to potential platelet count reduction.

 

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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