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Gliolan

Active Ingredient:
Aminolevulinic Acid Hydrochloride
Origin:
EU

Gliolan (Aminolevulinic Acid Hydrochloride)

Gliolan is an oral diagnostic agent whose active ingredient is aminolevulinic acid hydrochloride; the product is supplied in a tablet or liquid form (strength not specified) for use in the European market. It belongs to the oncologic diagnostic class and is prescribed by physicians to aid surgeons during fluorescence‑guided resection of malignant glioma. The compound is converted intracellularly to protoporphyrin IX, which fluoresces under blue light, highlighting tumor tissue.

Manufacturer / TM Owner

Photonamic Gmbh & Co. Kg

1
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Indications & Clinical Uses

Gliolan is indicated for fluorescence‑guided surgery of malignant glioma, helping neurosurgeons differentiate tumor tissue from normal brain during resection. The agent is administered orally prior to the operative procedure, allowing selective accumulation in tumor cells.

  • Enhances intraoperative visualization of high‑grade glioma under blue‑light excitation.
  • Supports more complete tumor removal while preserving surrounding healthy tissue.
  • Used in conjunction with standard imaging modalities such as MRI for surgical planning.
  • Applicable to adult patients with suspected or confirmed malignant glioma.
  • Facilitates documentation of fluorescence patterns for postoperative pathology correlation.

Side Effects

Adverse reactions to Gliolan are generally mild, but rare serious events have been reported; monitoring during and after surgery is recommended.

Common

  • Transient nausea or vomiting occurring shortly after oral intake of the agent.
  • Mild headache or dizziness experienced during the surgical procedure under blue light.
  • Temporary skin discoloration visible at the resection site when illuminated.
  • Light‑induced visual disturbances such as glare or reduced acuity during fluorescence imaging.

Serious

  • Severe photosensitivity reactions, including painful erythema, when exposed to intense light sources.
  • Allergic hypersensitivity manifesting as rash, pruritus, or angioedema requiring medical intervention.
  • Hepatic enzyme elevations indicating possible liver involvement, monitored via laboratory tests.
  • Acute renal impairment reported in isolated cases, necessitating renal function assessment.

Precautions & Warnings

When prescribing Gliolan, clinicians should evaluate patient history and procedural factors to minimize risk and ensure optimal fluorescence guidance.

  • Verify absence of known hypersensitivity to aminolevulinic acid or related compounds.
  • Assess liver and kidney function before administration, as impairment may affect drug metabolism.
  • Avoid exposure to strong ambient light for several hours after dosing to reduce photosensitivity.
  • Use appropriate protective eyewear for staff and patient during fluorescence imaging.
  • Consider pregnancy and lactation status; limited data are available, so weigh potential risks.
  • Coordinate timing of oral dose with planned surgical start to achieve peak tumor fluorescence.

Avoid Interactions

Gliolan may interact with other agents that influence porphyrin metabolism or photosensitivity; reviewing concomitant medications is recommended.

Avoid

  • Avoid concurrent use of photosensitizing drugs such as tetracyclines, sulfonamides, or certain chemotherapeutics.
  • Do not combine with other diagnostic agents that require blue‑light illumination, which could confound fluorescence interpretation.

Use with caution

  • Use with caution in patients receiving hepatic enzyme inducers or inhibitors, as they may alter protoporphyrin IX accumulation.
  • Caution is advised when administering anticoagulants, because intraoperative bleeding may affect fluorescence visibility.
  • Monitor closely when combined with agents that affect renal clearance, especially in patients with reduced kidney function.

Frequently Asked Questions

Gliolan contains aminolevulinic acid hydrochloride, which is metabolized inside cells to protoporphyrin IX. This compound accumulates preferentially in tumor cells and emits fluorescence when illuminated with blue light, allowing surgeons to distinguish malignant tissue from normal brain.

Gliolan is given orally as a single dose prior to the scheduled surgery. The timing is coordinated so that peak tumor fluorescence occurs during the operative procedure.

Gliolan is indicated for adult patients with suspected or confirmed malignant glioma who are undergoing surgical resection. Eligibility is determined by the treating neurosurgeon based on clinical and imaging findings.

Current labeling and clinical data primarily address adult use. Use in children should only be considered when the potential benefits outweigh the risks and after specialist evaluation.

Common adverse effects include transient nausea or vomiting, mild headache or dizziness during the procedure, temporary skin discoloration at the surgical site under blue light, and light‑induced visual disturbances.

Serious reactions, although rare, may include severe photosensitivity with painful erythema, allergic hypersensitivity such as rash or angioedema, hepatic enzyme elevations, and acute renal impairment.

Gliolan should not be used in patients with a known hypersensitivity to aminolevulinic acid or any of its excipients. Caution is advised in individuals with significant liver or kidney dysfunction.

Patients should avoid direct exposure to strong ambient or artificial light for several hours after the oral dose and wear protective clothing or sunglasses if exposure cannot be avoided.

Medications that are photosensitizing (e.g., tetracyclines, sulfonamides) or that affect porphyrin metabolism may interfere with Gliolan’s fluorescence. Clinicians should review all concurrent drugs and adjust therapy as needed.

The surgical team should record the timing of the oral dose, the fluorescence intensity observed, and any intra‑operative observations related to tumor visualization. This information supports postoperative pathology correlation and quality assurance.

Gliolan is marketed in the European Union. Availability in other regions depends on local regulatory approvals and may vary.

Standard postoperative imaging (MRI) is performed to assess the extent of resection. Laboratory monitoring of liver and kidney function may be considered if adverse effects were observed.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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