Fotoran E6 (Lyophilisate) Instructions for Use
ATC Code
L01XD (Sensitizing agents used for photodynamic/radiation therapy)
Pharmacotherapeutic Group
Antineoplastic agents; other antineoplastic agents; sensitizing agents used in photodynamic/radiation therapy
Pharmacological Action
Chlorin E6 selectively accumulates in pathological tissue (benign and malignant neoplasms of various origins and localizations, predominantly characterized by neovascularization) and, upon local exposure to light with a wavelength of 660-670 nm, provides a photosensitizing effect leading to damage of tumor tissue. Chlorin E6 is a highly informative diagnostic agent in spectrofluorescent studies.
Pharmacokinetics
After IV administration, the Cmax of Chlorin E6 in tumors is recorded after 3 hours, then its concentration slowly decreases. In vascular endothelial cells, the Cmax of Chlorin E6 is detected 10-15 minutes after the start of the infusion. Trace amounts of Chlorin E6 are detected in the blood 24 hours after IV administration. It penetrates well through tissue and cellular barriers and is detected in the thymus, skin, brain and bone marrow, spleen, ovaries, adrenal glands, heart, pancreas, stomach, kidneys, liver, and lungs.
Indications
In oncology: photodynamic therapy of malignant neoplasms – skin cancer (squamous cell and basal cell), melanoma, intradermal and subcutaneous metastases of melanoma, breast cancer and its intradermal metastases, cancer of the mucous membranes, including hollow organs (vulva, cervix (including cervical intraepithelial neoplasia grades I-III), esophagus, rectum, etc.); diagnosis of malignant neoplasms by the spectrofluorescent method.
In ophthalmology: photodynamic therapy in patients with central involutional chorioretinal dystrophy with classic choroidal involutional neovascularization, with subfoveal choroidal neovascularization in myopia.
ICD codes
| ICD-10 code | Indication |
| C15 | Malignant neoplasm of esophagus |
| C20 | Malignant neoplasm of rectum |
| C43 | Malignant melanoma of skin |
| C44 | Other malignant neoplasms of skin |
| C50 | Malignant neoplasm of breast |
| C51 | Malignant neoplasm of vulva |
| C53 | Malignant neoplasm of cervix uteri |
| H35.0 | Background retinopathy and retinal vascular changes |
| H35.3 | Degeneration of macula and posterior pole |
| Z03 | Medical observation and evaluation for suspected disease or pathological condition |
| ICD-11 code | Indication |
| 2B70.Z | Malignant neoplasm of esophagus, unspecified |
| 2B92.Z | Malignant neoplasm of rectum, unspecified |
| 2C30.Z | Melanoma of skin, unspecified |
| 2C31.Z | Squamous cell carcinoma of skin |
| 2C32.Z | Basal cell carcinoma of skin, unspecified |
| 2C33 | Skin adnexal carcinoma |
| 2C34 | Cutaneous neuroendocrine carcinoma |
| 2C35 | Sarcoma of skin |
| 2C3Z | Malignant neoplasms of skin of unknown or unspecified type |
| 2C65 | Hereditary breast and ovarian cancer syndrome |
| 2C6Y | Other specified malignant neoplasms of the breast |
| 2C6Z | Malignant neoplasms of breast, unspecified |
| 2C70.Z | Malignant neoplasms of vulva, unspecified |
| 2C77.Z | Malignant neoplasms of cervix uteri, unspecified |
| 9B78.1Z | Background retinopathy and retinal vascular changes, unspecified |
| 9B78.3Z | Degeneration of macula or posterior pole, unspecified |
| QA02 | Medical observation or examination for suspected diseases or conditions that were ruled out |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Administer Fotoran E6 intravenously as a slow infusion. Determine the dose individually based on the tumor type, size, and localization.
For skin cancers (basal cell, squamous cell carcinoma, melanoma), use a dose of 0.8-1.2 mg/kg body weight. For mucosal lesions (esophagus, rectum, cervix, vulva), administer 1.0-1.5 mg/kg.
In ophthalmology for choroidal neovascularization, use a dose of 1.0 mg/kg. Initiate laser light exposure at a wavelength of 660-670 nm after a 3-hour interval following infusion completion.
Reconstitute the lyophilisate immediately before use with 0.9% Sodium Chloride injection solution. Do not shake the vial vigorously; ensure complete dissolution.
Protect the reconstituted solution from light and administer promptly. Perform the entire procedure, from reconstitution to infusion, in a darkened room to prevent premature photosensitization.
Adverse Reactions
Possible increase in body temperature, pain in the irradiation zone (relieved by analgesic drugs), increased blood pressure in patients with concomitant diseases of the cardiovascular system. When administered in therapeutic doses, it has mild systemic phototoxicity. In the first week after administration of the drug, if the light regimen is violated, patients may develop hyperemia and edema of open body surfaces (without pigmentation).
Very rarely decreased visual acuity, visual field defects, lacrimation, subretinal hemorrhage, vitreous hemorrhage.
Contraindications
Hypersensitivity to the drug, severe renal or hepatic insufficiency, diseases of the cardiovascular system in the stage of decompensation; pregnancy, breastfeeding period; childhood.
Use in Pregnancy and Lactation
Contraindicated for use during pregnancy and breastfeeding.
Pediatric Use
Contraindicated for use in children.
Special Precautions
Starting from the first day of using Chlorin E6, open body surfaces should be treated with a photoprotective cream.
During the treatment period, it is necessary to avoid solar and ultraviolet radiation. The patient must be instructed on the need to strictly observe the light regimen (exposure to direct sunlight, watching television, etc. is excluded). The administration of Chlorin E6 should be carried out in a darkened room.
Effect on the ability to drive vehicles and mechanisms
Given the likelihood of side ophthalmological effects, activities requiring concentration and speed of psychomotor reactions should be avoided for 24 hours after the administration of Chlorin E6.
Drug Interactions
Concomitant use with analgesic agents is possible. The use of local anesthetics (infiltration anesthesia) is not recommended. Prescription of the drugs “bien”, reparaf, promotes early epithelialization of the wound defect, enhancement of connective tissue growth, and reduction of pain syndrome. Chlorin E6 should not be used simultaneously with drugs that affect photosensitivity (tetracycline and fluoroquinolone antibiotics, sulfonamides, phenothiazine derivatives, hypoglycemic drugs – sulfonylurea derivatives (glibenclamide, thiazide diuretics, griseofulvin) and other drugs with known photosensitizing activity).
Chlorin E6 should not be used simultaneously with drugs that may weaken the effectiveness of the treatment (beta-carotene, ethanol, mannitol). Simultaneous administration of drugs with known damaging effects on the liver, as well as those that may affect the metabolism of chlorin and prolong systemic phototoxicity (CYP3A4 inhibitors and inducers – cimetidine, ketoconazole, itraconazole, erythromycin, saquinavir, ritonavir, rifampicin) is excluded.
Storage Conditions
Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Rx Only
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Lyophilizate for the preparation of solution for infusion 50 mg: fl. 1 pc.
Marketing Authorization Holder
Ranpharma, LLC (Russia)
Manufactured By
Deko Company, LLC (Russia)
Dosage Form
| Fotoran E6 | Lyophilizate for the preparation of solution for infusion 50 mg: fl. 1 pc. |
Dosage Form, Packaging, and Composition
Lyophilizate for the preparation of solution for infusion greenish-black in color, in the form of a tablet.
| 1 vial | |
| Chlorin E6 trisodium salt6 (Photolon) | 50 mg |
Excipients : povidone K17, sodium hydroxide.
50 mg – vials (1) – cardboard packs.
Lyophilizate for the preparation of solution for infusion 100 mg: vial 1 pc.
Marketing Authorization Holder
Ranpharma, LLC (Russia)
Manufactured By
Deko Company, LLC (Russia)
Dosage Form
| Fotoran E6 | Lyophilizate for the preparation of solution for infusion 100 mg: vial 1 pc. |
Dosage Form, Packaging, and Composition
Lyophilizate for the preparation of solution for infusion greenish-black in color, in the form of a tablet.
| 1 vial | |
| Chlorin E6 trisodium salt6 (Photolon) | 100 mg |
Excipients : povidone K17, sodium hydroxide.
100 mg – vials (1) – cardboard packs.
