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2025-05-02 23:49
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Policy
New PVA operation system will be implemented from May
by
Lee, Tak-Sun
Apr 30, 2024 05:49am
The detailed operation standards for the Price-Volume Agreement negotiations will change drastically from May. The reduction rate will be applied differently depending on the amount of each drug¡¯s insurance claims, and products with annual claims of less than KRWk 3 billion will be excluded. In addition, the discount rate of drugs that ha
Policy
Gov¡¯t discloses draft for overseas drug price reevals
by
Lee, Tak-Sun
Apr 29, 2024 05:50am
The Korean government presented a draft of its plan during a meeting for the foreign drug price comparison reevaluations that was held on the 26th. The government¡¯s foreign drug price comparison reevaluation was planned by the government to adjust the price of off-patent drugs by comparing their price to the upper limit of A8 countries (Jap
Policy
Jardiance under review for expanding reimb to kidney disease
by
Lee, Tak-Sun
Apr 29, 2024 05:49am
'Jardiance tab (empagliflozin, Boehringer Ingelheim Korea),' SGLT-2 class of treatment, is considered for expanding reimbursement to kidney disease, in addition to its current reimbursement for diabetes and cardiac failure. As Forxiga, a competing drug in the same class as Jardiance, is expected to withdraw from the Korean market in the
Policy
Pharma companies with 'superior R&D¡¤K-made drug ingredients
by
Lee, Jeong-Hwan
Apr 26, 2024 05:48am
Starting this year, under the 2nd comprehensive National Health Insurance Plan (hereafter, referred to as NHI Plan), the government will provide preferential drug pricing for new drugs developed by pharmaceutical companies with high R&D costs. Additionally, the plan will expand the scope of the risk sharing agreement (RSA) for severe disea
Policy
Prolia and Ryaltris adjust drug pricing
by
Lee, Tak-Sun
Apr 23, 2024 05:40am
Amgen Korea and Chong Kun Dang Pharmaceutical will voluntarily reduce the price of 'Prolia,' which they are jointly selling. As the government expanded the administration guidance of osteoporosis medicines, Prolia, which is expected to see an increase in sales following the reimbursement expansion, voluntarily adjusted the ceiling price
Policy
HK inno.N starts developing a Lixiana generic
by
Lee, Hye-Kyung
Apr 23, 2024 05:36am
HK inno.N is joining the race to develop a generic version of the NOAC (novel oral anticoagulant) drug Lixiana (edoxaban). The Ministry of Food and Drug Safety recently approved clinical trials to evaluate the bioequivalence of the Lixiana generic ¡®IN-G00002¡¯ and IN-R00002 (Lixiana). The IN-G00002 bioequivalence trial will evaluate t
Policy
Atopic dermatitis drug Adtralza will be reimb in May
by
Lee, Jeong-Hwan
Apr 22, 2024 05:45am
Leo Pharma Korea¡¯s atopic dermatitis treatment, Adtralza (tralokinumab), will be reimbursed from May 1 in Korea. The reimbursement standards for osteoporosis drugs will also be improved, and patients who show some improvement in bone mineral density will be able to continue receiving reimbursement. As such, JW Pharmaceuticals' iron injec
Policy
KMPG ¡®We ask for the prompt reimbursement of Xpovio¡¯
by
Kim, Jung-Ju
Apr 22, 2024 05:45am
Patients¡¯ demand for the reimbursement listing of ¡®Xpovio 20mg (selinexor),¡¯ a new drug for multiple myeloma that was developed by the Chinese pharmaceutical company Antengene, is growing. The patients are claiming that they are becoming ¡®medical poor¡¯ due to the delay in the reimbursement of the only option available in the area. Xp
Policy
Will the 37th new drug in Korea receive approval?
by
Lee, Hye-Kyung
Apr 22, 2024 05:45am
The approval for the 37th new drug in Korea is approaching. According to industry sources on the 22th, the Ministry of Food and Drug Safety (MFDS) completed the safety and efficacy assessment of the three zastaprazan-containing products from Onconic Therapeutic, Jeil Healthscience, and Jeil Pharmaceutical. The completion of the safet
Policy
Reimb expansions of Keytruda have failed the 4th CDRC
by
Lee, Tak-Sun
Apr 19, 2024 06:24am
Keytruda¡¯s reimbursement expansion item did not cross the Cancer Disease Review Committee (CDRC) threshold for the fourth time following its expansion in June last year. The analysis is that this attempt is particularly significant as all 15 indications were reviewed by the CDRC, and MSD¡¯s financial contribution proposal was discussed f
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