Product image of Kayfanda (Odevixibat) supplied by GNH India

Kayfanda

Active Ingredient:
Odevixibat
Origin:
EU

Kayfanda (Odevixibat)

Odevixibat, the active ingredient in Kayfanda, is a Ileal bile acid transporter (IBAT) inhibitor presented as an oral formulation for oral use. It is indicated for the treatment of pruritus associated with progressive familial intrahepatic cholestasis (PFIC) and Alagille syndrome, conditions characterized by cholestatic liver disease.
GNH India supplies Kayfanda as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide, adhering to stringent quality standards and providing full regulatory documentation to streamline import, distribution and clinical use across global markets.

Manufacturer / TM Owner

Ipsen Pharma

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Indications & Clinical Uses

Kayfanda (odevixibat) acts on the bile acid transport pathway to relieve itching in cholestatic liver disorders.

  • Pruritus associated with progressive familial intrahepatic cholestasis (PFIC): reduces itch intensity and improves quality of life.
  • Pruritus associated with Alagille syndrome: alleviates severe itching symptoms in affected patients.
  • Cholestasis treatment: lowers serum bile acid concentrations, addressing the underlying cause of pruritus.

How It Works

  • Odevixibat selectively inhibits the ileal bile acid transporter (IBAT) located on the apical membrane of enterocytes in the distal ileum. By blocking this transporter, the drug reduces the re‑absorption of bile acids from the intestinal lumen, interrupting enterohepatic circulation. The resulting decrease in circulating bile acid levels diminishes the pruritic stimulus in cholestatic liver disease, thereby providing symptomatic relief for patients.

Side Effects

Adverse reactions reported with Kayfanda are generally related to its impact on gastrointestinal function and metabolic processes.

Common Side Effects

  • Diarrhea: frequent loose stools.
  • Abdominal pain: cramping or discomfort in the stomach area.
  • Nausea: feeling of sickness or urge to vomit.

Serious or Rare Side Effects

  • Elevated liver enzymes: indicates potential liver injury.
  • Severe dehydration: due to excessive fluid loss from diarrhea.
  • Allergic reaction: rash, swelling, or difficulty breathing.
  • Pancreatitis: inflammation of the pancreas presenting with severe abdominal pain.

Precautions & Warnings

When prescribing Kayfanda, clinicians should consider several precautionary measures to ensure patient safety.

  • Monitor liver function: perform baseline and periodic liver enzyme tests.
  • Assess hydration status: ensure adequate fluid intake to prevent dehydration.
  • Avoid use in patients with known hypersensitivity to odevixibat or excipients.
  • Use caution in severe renal impairment: adjust monitoring and consider risk‑benefit.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Kayfanda may interact with other medicines that affect bile acid metabolism or drug absorption.

Major Interactions (Avoid)

  • Bile acid sequestrants: can bind odevixibat and markedly reduce its absorption.
  • Strong CYP3A4 inducers: may decrease odevixibat plasma concentrations and efficacy.
  • Concomitant use with cholestyramine: interferes with drug bioavailability.

Moderate Interactions (Monitor Closely)

  • Antacids: may alter gastrointestinal pH and affect odevixibat absorption.
  • High‑fat meals: can modify the rate of drug uptake and require timing adjustments.

Frequently Asked Questions

Kayfanda contains odevixibat and is prescribed to treat severe itching (pruritus) associated with progressive familial intrahepatic cholestasis (PFIC) and Alagille syndrome, both of which are cholestatic liver disorders that cause elevated bile acid levels.

Odevixibat blocks the ileal bile acid transporter (IBAT) in the distal ileum, preventing re‑absorption of bile acids. This interruption reduces circulating bile acid concentrations, which in turn lessens the itch stimulus that characterises cholestatic liver disease.

The dosage of Kayfanda is individualized. A qualified prescriber determines the appropriate dose and dosing schedule based on the patient’s age, weight, disease severity, and clinical response.

Safety data for odevixibat during pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision should be made by the treating physician.

To order Kayfanda, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

The primary alternative for cholestatic pruritus is ursodeoxycholic acid, which works by altering bile composition. Odevixibat targets the IBAT pathway, directly reducing bile acid re‑absorption. Clinical experience suggests that IBAT inhibition can provide more rapid itch relief in PFIC and Alagille syndrome, though individual response varies.

Kayfanda should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, excessive heat and direct sunlight to maintain its stability and potency.

Kayfanda is taken orally, usually as a tablet or capsule, with or without food as directed by the prescribing clinician. Patients should follow the specific administration instructions provided on the prescription label.

Serious risks include elevated liver enzymes indicating possible liver injury, severe dehydration from persistent diarrhea, allergic reactions such as rash or breathing difficulty, and rare cases of pancreatitis. Patients should seek immediate medical attention if any of these symptoms develop.

Kayfanda should be avoided in individuals with known hypersensitivity to odevixibat or any of its excipients, and caution is advised in patients with severe hepatic impairment. The drug is also not recommended for use in patients where the risk‑benefit profile is unfavorable, as determined by their healthcare provider.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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