
NephLong
Imanix
Details
400 mg
Imanix 400 mg is a tyrosine kinase inhibitor manufactured by Beacon Pharmaceuticals Ltd. It contains imatinib mesylate, a targeted therapy used in oncology
🧫 Mechanism of Action
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Inhibits BCR‑ABL tyrosine kinase, the abnormal enzyme produced by the Philadelphia chromosome in chronic myeloid leukemia (CML).
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Also targets c-KIT and PDGF receptors, crucial in other cancers like GI stromal tumors (GIST) and hypereosinophilic syndrome.
✅ Approved Indications
Imanix 400 mg is indicated for treatment in:
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Chronic myeloid leukemia (Ph+ CML) across chronic, accelerated, and blast phases
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Acute lymphoblastic leukemia (Ph+ ALL)
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Gastrointestinal stromal tumors (GIST) — unresectable, metastatic, or adjuvant
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Myelodysplastic/myeloproliferative diseases, systemic mastocytosis, hypereosinophilic syndrome/chronic eosinophilic leukemia, dermatofibrosarcoma protuberans, and more
💊 Dosage & Administration
| Condition | Typical Adult Dose |
|---|---|
| CML chronic phase | 400 mg once daily |
| CML accelerated/blast crisis & Ph+ ALL | 600 mg once daily |
| GIST (unresectable/metastatic/adjuvant) | 400 mg once daily |
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Pediatric dosing: typically 340 mg/m²/day
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Taken with food and a large glass of water. 800 mg doses are split (400 mg twice daily) to optimize absorption.
⚠️ Precautions & Interactions
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CYP3A4 metabolism: strong inducers reduce levels; strong inhibitors (e.g., grapefruit juice) increase levels. Adjust dosage accordingly.
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May interact with warfarin and other CYP-metabolized drugs — monitor closely.
📋 Pharmacokinetics
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Bioavailability: ~98%, with peak plasma levels in 2–4 hours.
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Protein binding: ~95%.
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Half-life: ~18 hours; active metabolite CGP74588 ~40 hours.
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Excretion: ~81% within 7 days, mostly fecal, some urinary.
💾 Storage & Handling
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Store < 30 °C, in a cool, dry, light‑protected place. Keep out of children’s reach.
⚕️ Side Effects & Patient Advice
Common side effects include:
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Gastrointestinal issues (nausea, diarrhea, abdominal pain)
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Fatigue, muscle cramps, edema, rash
Important guidance:
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Avoid breastfeeding and pregnancy unless absolutely necessary
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Caution for liver or kidney impairment; dose adjustment may be needed
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May cause dizziness—avoid driving until response is known
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Skip missed doses; do not double dose.
Keto Nephron™ DS is a Medical Food as defined under 21 U.S.C. §360ee(b)(3) and 21 CFR 101.9(j)(8), formulated for the dietary management of Chronic Kidney Disease (CKD) Stages 3-5 in adults following physician-supervised protein-restricted diets. It is not a drug, not a dietary supplement, and is not intended for self-medication or general wellness use. MUST BE USED UNDER MEDICAL SUPERVISION. Quantum LifeSciences Inc., Claremont, CA 91711, USA. FDA Food Facility (Manufacturer) Reg. No. 14961463490.