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[News] Publication of Review Result of the Fifth Pharmaceutical Reimbursement Evaluation Committee of 2022
  • Date2024-09-06

Publication of Review Result of the Fifth Pharmaceutical Reimbursement Evaluation Committee of 2022

 

The Health Insurance Review and Assessment Service (President Kim Sun-min) releases the results of the deliberations of the 5th Pharmaceutical Reimbursement Evaluation Committee in 2022 as follows.

 

 ○ Result of the review of the adequacy of the healthcare benefit for the pharmaceutical applied for assessment

 
 

Product

Pharmaceutical company

Efficacy and effectiveness

Deliberation results

 

Zolgensma Inj.

(Onasemnogene abeparvovec)

Novartis Korea Ltd

Patient with spinal muscular atrophy (SMA) with a biallelic mutation in the SMN1 gene

Reimbursement is adequate.

*If healthcare benefit is pre- authorized, and patient-level performance-based risk sharing and total amount limit apply.

Fexuclue Tab 40mg etc 4 product

(Fexuprazan hydrochloride)

Daewoong Pharmaceutical co. Ltd,

Daewoongbio co. Ltd,

Hanall Biopharma co. Ltd,

In Therapeutics co. Ltd

Treatment of erosive gastroesophageal reflux disease (GERD)

Reimbursement is adequate when accepted at or below assessed value.

Donepezil/Donesive Patch 87.5 175mg (Donepezil)

CELLTRION Inc,

icure pharmaceutical & cosmetics co. Ltd

Treating symptoms of Alzheimer's type dementia

Reimbursement is adequate when accepted at or below assessed value.

Emgality 120 mg

/Milliliter pre-filled pen,Pre-filled syringe

(Galcanezumab, Recombinant DNA)

Eli Lilly and Company Korea

Prevention of migraine in adults

Reimbursement is adequate.

 Pursuant to Article 11(2) of the Rules on the Criteria for National Health Insurance Reimbursement, the President of the Health Insurance Review and Assessment Service evaluates the adequacy of reimbursement for drugs after deliberation by the Pharmaceutical Reimbursement Evaluation Committee. The final evaluation results may be subject to change if there are changes in the detailed reimbursement scope and items of the drug, changes in the approval of the item applied for decision, or revocation (cancellation) of the approval.
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