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2025-09-11 00:01
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"Increasing role of Kisqali in breast cancer therapy"
by
Whang, byung-woo
Feb 24, 2025 05:51am
The introduction of CDK 4/6 inhibitors has changed the treatment paradigm for metastatic breast cancer, addressing previously unmet needs. The introduction of a new treatment option has been positively evaluated because the existing endocrine therapy, which is used as first-line treatment for HR+/HER2 advanced and metastatic breast cancer, ac
Company
Will Prevnar 20 be included in NIP in 1H 2025?
by
Whang, byung-woo
Feb 24, 2025 05:51am
Pfizer is seeking to release Pfizer¡¯s new pneumococcal vaccine, Prevenar 20, in the first half of this year with its inclusion in the National Immunization Program (NIP) for children. According to industry sources, the Korea Disease Control and Prevention Agency and Pfizer have made progress in discussions on whether Prevnar20 should be
Company
Primary biliary cholangitis drug Iqirvo to land in Korea
by
Eo, Yun-Ho
Feb 24, 2025 05:51am
The new drug for primary biliary cholangitis Iqirvo may soon be launched in Korea. According to industry sources, Ipssen Korea is in the process of obtaining marketing authorization from the Ministry of Food and Drug Safety for Iqirvo (elafibranor), a dual peroxisome proliferator-activated receptor (PPAR) alpha/delta (PPAR ¥á, ¥ä) agonist
Company
Pricing negotiations for Vocabria+Rekambys combo complete
by
Eo, Yun-Ho
Feb 24, 2025 05:51am
The long-acting HIV drug Vocabria+Rekambys combination therapy is on the verge of being reimbursed in Korea, 2 years after its approval. According to industry sources, GSK Korea recently concluded drug price negotiations with the National Health Insurance Service for the combination therapy of the new HIV drugs Vocabria (cabotegravir) and
Company
Asthma drug Tezspire ready for launch
by
Whang, byung-woo
Feb 21, 2025 05:56am
Tezspire (tezepelumab), an anti-TSLP therapy for the treatment of severe asthma, is entering the market with its effectiveness regardless of biomarker status. Although the drug still faces reimbursement hurdle, clinical practices have high hopes. They expect that Tezspire's versatility can change the current treatment paradigm in which drug
Company
The aftermath of the prolonged medical care gap continues
by
Moon, sung-ho
Feb 20, 2025 05:59am
Global pharmaceutical companies are launching new blood cancer drugs in Korea one after another, but the situation on site is impeding their access. According to industry sources on the 17th, the the medical school admission expansion policy last year has led to a continued mass resignation of residents, which has disrupted the treatment of b
Company
Jeil¡¯s super-antibiotic cefiderocol approved in Korea
by
Nho, Byung Chul
Feb 20, 2025 05:59am
Jeil Pharmaceutical (CEO Seok-je Sung) announced on the 19th that it has received approval from the Ministry of Food and Drug Safety to market the drug Fetroja Inj 1g¡¯ (cefiderocol sulfate tosylate) for the treatment of multidrug-resistant gram-negative bacterial infections. With the approval, adult patients may use Fetroja for the trea
Company
Myelofibrosis drug 'Omjjara' attempts at reimb listing
by
Eo, Yun-Ho
Feb 20, 2025 05:59am
'Omjjara,' a targeted treatment for myelofibrosis, attempts to be added to the National Health Insurance reimbursement list. According to industry sources, GSK Korea submitted a reimbursement application for its new myelofibrosis drug, Omjjara (momelotinib), at the end of last year, and is awaiting to be considered for the Health Insuranc
Company
Organon Korea releases first product after spinoff
by
Whang, byung-woo
Feb 20, 2025 05:58am
Organon Korea is launching a new product for the first time since its spin-off in June 2019 and is beginning to expand its influence in earnest. The product, which was unveiled about 3 years after the official launch of the Korean subsidiary, is JADA, a medical device used to control and treat postpartum hemorrhage. The company plans to targe
Company
Celltrion¡¯s Prolia and Xgeva biosimilars approved in Europe
by
Chon, Seung-Hyun
Feb 19, 2025 05:56am
On the 18th, Celltrion announced that it had received marketing authorization from the European Commission for Stobocolo and Osenvelt, which are biosimilar versions of Prolia and Xgeva, respectively. The final approval was granted 2 months after the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA
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