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2025-05-04 09:44
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Policy
'Eutropin¡¤Biktarvy' price drop amid sales hike
by
Lee, Tak-Sun
Nov 6, 2024 05:52am
Due to the increased volume of usage, drug pricing for 'Eutropin Inj (somatropin, LG Chem)' and 'Biktarvy (Bictegravir/Emtricitabine/Tenofovir Alafenamide, Gilead Science),' which recently showed a sales hike, is expected to be reduced. Sources said on November 5th that the Health Insurance Review and Assessment Service (HIRA) recently
Company
20-valent pneumococcal conjugate vaccine set to launch
by
Moon, sung-ho
Nov 6, 2024 05:52am
Attention has been drawn to another competitor set to launch in the market for the 'pneumococcal vaccine.' This year, the pneumococcal vaccine market has been fiercely competitive with newly released products. As the 20-valent vaccine is likely to come out right after the 15-valent conjugate vaccine has entered the market after 13 years, comp
Company
Roche seeks digital solutions for its healthcare ecosystem
by
Whang, byung-woo
Nov 6, 2024 05:52am
With the importance of personalized healthcare being emphasized more than ever with the emergence of innovative new drugs, Roche Diagnostics Korea is aiming to lead the market by focusing on digital solutions. The company plans to lead the healthcare sector through digital transformation in line with the paradigm shift in treatment, from earl
Company
CKD¡¯s CKD-508 receives approval to initiate P1T in the U.S.
by
Son, Hyung Min
Nov 6, 2024 05:52am
Chong Kun Dang announced on the 4th that it has received approval from the U.S. Food and Drug Administration (FDA) for the Phase I clinical trial of CKD-508, its new drug candidate for dyslipidemia. In the trial, Chong Kun Dang will confirm the safety and lipid-improving effects of CKD-508 and explore the optimal dose for a Phase II trial
Policy
How will the new drug review process change with fee hike?
by
Lee, Hye-Kyung
Nov 6, 2024 05:52am
The Ministry of Food and Drug Safety (MFDS) announced plans to raise the fee for new drug approvals to KRW 410 million from January 1 next year. The agency has prepared the approval and review process to implement the plan and has begun collecting industry opinion. According to MFDS¡¯s press corp coverage, the MFDS recently delivered a revise
Company
Amgen's Prolia¡¤Evenity generate KRW 2T in quarterly sales
by
Son, Hyung Min
Nov 6, 2024 05:52am
Amgen's Prolia and Evenity for the treatment of osteoporosis continue to show sales growth. Prolia and Evenity led Amgen's performance, generating sales of KRW 2 trillion in Q3. Analysis suggests that sequential therapy, using Evenity followed by Prolia for the treatment of osteoporosis with high-risk fractures, has been widely used, and it
Company
Chong Kun Dang speeds up dyslipidemia drug development
by
Son, Hyung Min
Nov 5, 2024 05:46am
&160; Chong Kun Dang is accelerating the development of new drugs for dyslipidemia. The company has received approval to initiate a second global clinical trial in 10 years for its new drug candidate 'CKD-508' since the company began its research in 2014. According to industry sources on the 4th, Chong Kun Dang recently received approva
Company
¡®Prevent MI recurrence through efficient LDL-C control'
by
Whang, byung-woo
Nov 5, 2024 05:45am
With the rise of metabolic diseases such as hypertension, diabetes, and hyperlipidemia increase in Korea, the prevalence of myocardial infarction and atherosclerotic cardiovascular diseases are also on the rise. The mortality rate of myocardial infarction is in the 20-30% range when it occurs for the first time, but the mortality rate increas
Company
New oHCM drug 'Camzyos' nearing approval for reimb in KOR
by
Eo, Yun-Ho
Nov 5, 2024 05:45am
'Camzyos,' a new drug to treat obstructive hypertrophic cardiomyopathy (oHCM), is nearing 90% approval for insurance reimbursement listing. Sources said that BMS Pharmaceutical Korea and the National Health Insurance Service (NHIS) concluded drug pricing negotiations for Camzyos (mavacamten), a new drug for obstructive hypertrophic cardi
Policy
Reimb standards that prevent abuse of HA Eye Drops imminent
by
Lee, Tak-Sun
Nov 5, 2024 05:45am
Health authorities are expected to establish reimbursement standards to prevent the misuse of hyaluronic acid eye drops after failing to reach a conclusion during last year's reimbursement adequacy evaluations. It is reported that the Ministry of Health and Welfare is preparing an administrative notice to announce the reimbursement standar
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