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AstraZeneca India Secures Regulatory Approval for Novel Hyperkalaemia Treatment Lokelma

7 months ago2 min read

Key Insights

  • AstraZeneca Pharma India has received CDSCO approval to import and market sodium zirconium cyclosilicate (Lokelma) for treating high potassium levels in adult patients.

  • The approved formulation will be available in 5g and 10g doses as an oral suspension powder, expanding treatment options for hyperkalaemia management in India.

  • This regulatory milestone follows AstraZeneca's earlier approval for Durvalumab (Imfinzi) in cancer treatment, demonstrating the company's expanding presence in the Indian pharmaceutical market.

The Indian pharmaceutical landscape is set to welcome a new treatment option for hyperkalaemia as AstraZeneca Pharma India receives crucial regulatory approval for its novel therapy. The Central Drugs Standard Control Organisation (CDSCO) has granted permission to import and market sodium zirconium cyclosilicate powder, marketed under the brand name Lokelma, for treating elevated potassium levels in adult patients.

Treatment Specifications and Formulation

The approved medication will be available as an oral suspension powder in two dosage strengths - 5g and 10g. Lokelma represents a significant addition to the therapeutic arsenal for managing hyperkalaemia, a serious condition characterized by elevated potassium levels in the blood that can lead to severe complications if left untreated.

Regulatory Pathway and Market Impact

The CDSCO approval marks a crucial milestone in bringing this important medication to Indian patients. However, AstraZeneca notes that the actual launch remains contingent upon receiving additional statutory approvals. This development follows the company's recent regulatory success with Durvalumab (Imfinzi), their cancer treatment solution, highlighting AstraZeneca's commitment to expanding their therapeutic portfolio in India.

Market Response and Company Performance

The announcement has been well-received by the market, with AstraZeneca's shares showing positive movement on the National Stock Exchange. The company's stock closed 1.73% higher at Rs 7,466.65 per share, outperforming the benchmark Nifty index which advanced by 0.93%. However, it's worth noting that the company's stock has experienced a 38.39% decline over the past twelve months.

Clinical Significance

Hyperkalaemia management remains a critical concern in clinical practice, particularly among patients with kidney disease, heart failure, or those taking certain medications that can affect potassium levels. The introduction of Lokelma provides healthcare providers with an additional treatment option, potentially improving patient care outcomes in the management of this serious electrolyte disorder.
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