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Active Pharma Ingredients / 24 Sep 2026

CUSTIRSEN

Generic Name: CUSTIRSEN

ABSTRACT -

Custirsen is an investigational antisense oligonucleotide designed to reduce clusterin expression. Clusterin is associated with cell-survival signaling and treatment resistance; downregulation was investigated as a chemosensitizing strategy in prostate cancer and other malignancies.

DOSAGE -

No approved standard dose is established. Oncology studies evaluated intravenous custirsen sodium, including a 640 mg weekly regimen combined with docetaxel and prednisone in metastatic castration-resistant prostate cancer trials.

SIDE EEFECTS -

  • Fever, chills, rigors, fatigue, or flu-like symptoms
  • Nausea, vomiting, anorexia, or mucositis
  • Anemia, thrombocytopenia, leukopenia, or neutropenia
  • Dyspnea, pleural effusion, or fluid-related symptoms in susceptible patients
  • Injection/infusion-related reactions and laboratory abnormalities

ALLERGIC REACTIONS -

(These symptoms may indicate an allergic reaction and require medical attention.)

  • Rash, itching, hives, or flushing
  • Swelling of the face, lips, tongue, or throat
  • Breathing difficulty, wheezing, or chest tightness
  • Severe dizziness, hypotension, or anaphylaxis

DRUG INTERACTIONS-

  • Combination with cytotoxic chemotherapy may increase myelosuppression and infection risk
  • Anticoagulants or antiplatelet drugs may require closer monitoring if platelet counts fall
  • Nephrotoxic or fluid-retaining medicines may complicate tolerability
  • Drug interactions are incompletely defined because custirsen remains investigational

PREAUTONS–

  • Use only under oncology specialist supervision or a clinical trial protocol
  • Monitor blood counts, renal/hepatic function, fluid status, and respiratory symptoms
  • Assess infection risk and manage fever or neutropenia promptly
  • Pregnancy and lactation safety are not established
  • Confirm oligonucleotide identity by sequence/backbone chemistry rather than by a conventional small-molecule drawing

WARNINGS –

  • Investigational agent with no routine approved therapeutic use in many jurisdictions
  • Serious cytopenias, infections, dyspnea, or effusions may occur with combination therapy
  • Not interchangeable with cysteine/cystine nutritional products or other antisense oligonucleotides
  • Clinical trials did not establish a survival benefit in some late-stage prostate cancer settings

Have any questions? or Need help Contact us – 022 6163 6163 | support@medicus.com

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