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.

Pamiparib Characteristics
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Ingredients: Pamiparib
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Properties: The capsule shell is opaque. The contents are yellow pellets
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Packaging Specification: Available Strength: 20 mg/capsule (calculated as C₁₆H₁₅FN₄O); Package Size: 60 capsules per bottle/box
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Storage: Store at room temperature (details not explicitly found in sources; general recommendation is 20-25°C)
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Expiry Date: To be stated on the specific packaging based on the manufacturing date, typically 24-36 months
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Executive Standard: Complies with the quality standards approved by the National Medical Products Administration (NMPA) of China
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Approval Number: Approved by the National Medical Products Administration (NMPA) in China
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Date of Revision: Approved by the National Medical Products Administration (NMPA) in China
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Manufacturer: BeiGene Ltd
Guidelines for the Use of Pamiparib
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Dosage and Administration:
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Recommended Dose: 40 mg taken orally twice daily.
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Administration: Swallow capsules whole with or without food.
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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.
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Adverse Reactions:
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Common Adverse Reactions:
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Blood and lymphatic system disorders: Anemia, leukopenia, neutropenia, thrombocytopenia, lymphocytopenia.
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Gastrointestinal disorders: Nausea, vomiting, diarrhea, abdominal pain, decreased appetite.
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General disorders and administration site conditions: Fatigue.
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Investigations: Increased AST, increased ALT, increased blood bilirubin.
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Serious Adverse Reactions:
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Myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) have been reported with PARP inhibitors.
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Severe hematological toxicities (e.g., severe anemia, neutropenia, thrombocytopenia).
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If serious adverse reactions occur, dose interruption, reduction, or discontinuation may be necessary.
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Contraindications: Hypersensitivity to pamiparib or any component of the formulation.
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Precautions:
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Use with caution in patients with hepatic or renal impairment.
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Not recommended during pregnancy or breastfeeding.
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Effective contraception is advised for women of childbearing potential during and after treatment.
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Pamiparib Interactions
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CYP3A Inhibitors: Co-administration may increase pamiparib levels, potentially enhancing side effects.
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CYP3A Inducers: Co-administration may decrease pamiparib efficacy.
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Other Chemotherapeutic Agents: Concurrent use may exacerbate hematological toxicities.
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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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