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2025-10-26 18:51
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Company
Trelegy 200 Ellipta may be prescribed at tertiary hospitals
by
Eo, Yun-Ho
Jun 25, 2024 05:46am
The double dose Trelegy Ellipta, which received approval in Korea for asthma, not COPD, may now be prescribed at general hospitals in Korea. According to industry sources, GSK Korea's Trelegy Ellipta (fluticasone furoate/umeclidinium/vilanterol) has passed the drug committees (DCs) of the Big 5 tertiary hospitals in Korea, including Sam
Company
'Camzyos' receives DREC¡¯s reconsideration decision
by
Eo, Yun-Ho
Jun 25, 2024 05:46am
The final decision was not reached on the first attempt. The path to getting 'Camzyos,' the first novel drug for obstructive hypertrophic cardiomyopathy (oHCM), listed for reimbursement seems to be challenging. According to the industry sources, BMS Korea¡¯s Camzyos (mavacamten), a novel drug used to treat obstructive hypertrophic cardio
Policy
LG Chem and Samsung Bioepis's biosimilars are reimbursed
by
Lee, Tak-Sun
Jun 25, 2024 05:46am
LG Chem and Samsung Bioepis¡¯ biosimilar products will be listed for reimbursement in July. LG Chem is launching a biosimilar of the autoimmune disease treatment Humira, and Samsung Bioepis is launching a biosimilar of Stelara. Both are aiming to list at the lowest price to compete with their respective original products. According to i
Policy
Combinatory drugs with linagliptin+dapagliflozin
by
Lee, Tak-Sun
Jun 25, 2024 05:46am
Following the patent expiration of DPP-4 inhibitor Trajenta (linagliptin), combinatory drugs containing linagliptin have been released. Next month, a combinatory drug containing linagliptin combined with SGLT-2 inhibitory dapagliflozin will enter the market. It is a combinatory drug with a new combination being introduced in South Korea. Acco
Opinion
[Reporter's View] No more exemptions, just deferrals
by
Eo, Yun-Ho
Jun 24, 2024 05:47am
The Korean government has set out to fix the pharmacoeconomic evaluation exemption system. Although the authorities coined it as an ¡°improvement,¡± the direction seems to be near a ¡°reduction.¡± A report on a study commissioned by the Health Insurance Review and Assessment Service was released at the end of last year. The study, titled
Policy
Will GMP One-strike-out be loosened?...MFDS, 'negative'
by
Lee, Hye-Kyung
Jun 24, 2024 05:47am
While pharmaceutical companies advocate for loosening the 'Cancellation of the GMP compliance decision' act, the Ministry of Food and Drug Safety (MFDS) says it will start a discussion once it receives an official submission of opinions. This is in response to biopharmaceutical companies¡¯ submission of a statement last month regarding t
Company
K-Bios make bid into pancreatic cancer treatment environment
by
Son, Hyung-Min
Jun 24, 2024 05:47am
The domestic pharmaceutical and bio-industry has made a bid into the development of new drugs for pancreatic cancer through the use of combination therapy. Despite the development of various treatments to date, the five-year survival rate of pancreatic cancer has remained the lowest among the top 10 cancers, at 12.6%. Pancreatic cancer is diffic
Policy
Price of BI¡¯s diabetes drug Trajenta is cut 30% from July
by
Lee, Tak-Sun
Jun 24, 2024 05:46am
Price of Boehringer Ingelheim¡¯s flagship diabetes drugs ¡®Trajenta¡¯ and ¡®Jardiance¡¯ will both be cut in July. Trajenta will receive an ex officio price cut due to the entry of its generic while Jardiance will see a price cut after completing price-volume agreement (PVA) negotiations. According to industry sources on the 21st, the i
Company
Pfizer reapplies for reimb listing of Vyndamax in Korea
by
Eo, Yun-Ho
Jun 21, 2024 05:47am
¡®Vyndamax,¡¯ a new drug for transthyretin&160;amyloid cardiomyopathy (ATTR-CM), is again attempting reimbursement listing in Korea. According to industry sources, Pfizer Korea had recently submitted an application for the insurance reimbursement of Vyndamax, its new drug for transthyretin amyloid cardiomyopathy (ATTR-CM). Vyndamax f
Policy
Low-dose 'nicergoline' is increasingly becoming available
by
Lee, Hye-Kyung
Jun 21, 2024 05:47am
Old drugs containing the active ingredient 'nicergoline' are on the rise for substituting 'choline alfoscerate,' which is under reassessment of clinical and reimbursement. The lower doses are also being approved. Previously, companies mostly received approvals for items containing 30 mg doses, which obtained indications for the first-l
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