Iminod

 5% Cream
Ziska Pharmaceuticals Ltd.

10 gm tube: ৳ 275.00

Indications
  • Actinic Keratosis (AK): Treatment of multiple non-hyperkeratotic, non-hypertrophic actinic keratoses on the face or scalp in immunocompetent adults.
  • Superficial Basal Cell Carcinoma (sBCC): Treatment of biopsy-confirmed primary superficial basal cell carcinoma in adults where surgical methods are not appropriate.
  • External Genital and Perianal Warts: Management of external genital and perianal warts (condyloma acuminata) in patients aged 12 years and older.

Off-label Uses:

  • Bowen’s disease (squamous cell carcinoma in situ)
  • Molluscum contagiosum
  • Certain other superficial skin cancers and viral skin infections
Dosage & Administration
  • Route: Topical
  • Actinic Keratosis: Apply a thin layer to affected area twice weekly (e.g., Monday and Thursday) at bedtime for 16 weeks.
  • Superficial Basal Cell Carcinoma: Apply once daily, five times per week (e.g., weekdays) at bedtime for 6 weeks.
  • External Genital and Perianal Warts: Apply once daily, three times per week (e.g., Monday, Wednesday, Friday) at bedtime for up to 16 weeks.

Instructions:

  • Apply to clean, dry skin.
  • Rub gently until cream disappears.
  • Leave on skin for 6–10 hours before washing off.
  • Avoid occlusive dressings unless directed.

Special Populations:

  • Safety in children under 12 not established.
  • No dose adjustment necessary for elderly or those with renal/hepatic impairment.
Mechanism of Action (MOA)

Imiquimod acts as an immune response modifier by binding to Toll-like receptor 7 (TLR7) on antigen-presenting cells, stimulating the release of cytokines including interferon-alpha, tumor necrosis factor-alpha, and various interleukins. This cytokine cascade enhances innate and adaptive immune responses, promoting the clearance of virus-infected and tumor cells at the site of application.

Pharmacokinetics
  • Absorption: Minimal systemic absorption after topical application; plasma levels typically undetectable.
  • Distribution: Localized primarily to application site; systemic distribution negligible.
  • Metabolism: Not significantly metabolized systemically due to minimal absorption.
  • Excretion: Unknown; presumed local metabolism and elimination via skin turnover.
  • Onset: Immunologic effects begin shortly after application; clinical response typically observed over weeks.
Pregnancy Category & Lactation
  • Pregnancy: Category C – Animal studies show adverse fetal effects at high doses; human data insufficient. Use only if benefits outweigh risks.
  • Lactation: Unknown if excreted in human milk; due to minimal systemic absorption, risk to infant likely low. Caution advised.
  • Recommendation: Use only if clearly necessary; avoid application on breast tissue during breastfeeding.
Therapeutic Class
  • Immune response modifier
  • Topical antiviral and antitumor agent
Contraindications
  • Hypersensitivity to imiquimod or formulation excipients
  • Application to mucous membranes, eyes, nostrils, or ears
  • History of autoimmune skin disorders at the treatment site
Warnings & Precautions
  • Monitor for severe local skin reactions (erythema, erosion, ulceration). Interrupt or reduce frequency if necessary.
  • Rare systemic flu-like symptoms have been reported.
  • Use cautiously in patients with autoimmune diseases.
  • Avoid contact with eyes and mucous membranes.
  • Safety in immunocompromised patients not established.
Side Effects
  • Common: Local erythema, scaling, flaking, pruritus, burning, pain, crusting, and ulceration at application site.
  • Less common: Hypo- or hyperpigmentation, secondary infections, rare systemic flu-like symptoms.
  • Side effects usually begin within 1–2 weeks and resolve after treatment cessation or dose adjustment.
Drug Interactions
  • No significant systemic drug interactions due to minimal absorption.
  • Avoid concurrent use with other topical immunomodulators or irritants at the treatment site.
  • No known food or alcohol interactions.
Recent Updates or Guidelines
  • Confirmed role as a non-invasive alternative to surgery for superficial basal cell carcinoma and actinic keratosis.
  • Continued recommendation as first-line topical treatment for external genital warts.
  • Emphasis on patient counseling to manage local skin reactions and improve adherence.
  • Ongoing studies for expanding indications in dermatologic viral and neoplastic conditions.
Storage Conditions
  • Store at 20°C to 25°C (68°F to 77°F).
  • Protect from moisture and light.
  • Keep container tightly closed.
  • Do not freeze.
  • Follow manufacturer instructions for discard after opening.
Available Brand Names