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Vyndamax tries RSA after failing essential drug designation

By Eo, Yun-Ho | translator Alice Kang

21.04.14 15:02:09

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Submitted supplemented data after PE assessment ¡¦ a matter of whether the company reaches an agreement with the government

The only ATTR-CM treatment option ¡¦ proven to reduce death in the Phase 3 trial



Once again, attempts are in progress to receive reimbursement for 'Vyndamax,' a new drug for the treatment of transthyretin amyloid cardiomyopathy (ATTR-CM).

Industry sources said that Pfizer Korea had recently submitted an application for the reimbursement of its new ATTR-CM drug, Vyndamax (tafamidis 61mg). This time, the company conducted the PE assessment and aims to receive reimbursement through the risk-sharing agreement (RSA) scheme.

After failing to receive designation as an essential drug earlier this year, the company has quickly supplemented the data to try for reimbursement once again, which shows the company¡¯s determination to be listed for reimbursement.

Eo, Yun-Ho(unkindfish@dailypharm.com)
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