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2025-05-02 23:07
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Company
"Paradigm shift in follicular lymphoma treatment: CAR-T"
by
Whang, byung-woo
Feb 13, 2025 05:58am
"Although CAR-T cell therapy or bispecific antibody respectively offers an advantage for treating follicular lymphoma, CAR-T data demonstrating positive results over 10 years in 60% of patients indicate that it is an effective treatment option." As various treatment options are introduced to treat relapsed/refractory follicular lymphoma (FL)
Company
Celltrion wins, Samsung loses Eylea patent trial
by
Kim, Jin-Gu
Feb 13, 2025 05:58am
Companies have seen mixed results regarding the preliminary injunction applications over the biosimilar version of the macular degeneration drug Eylea (aflibercept). While Samsung Bioepis lost the preliminary injunction application for patent infringement filed by Bayer, Celltrion won its case. The conflicting results have also led to
Company
Officially launched Vantive Korea targets renal care market
by
Whang, byung-woo
Feb 13, 2025 05:58am
As Baxter's 'Renal Care and Acute Therapies Businesses' launches as an independent global company completes, it has begun officially operating under a new company name. According to medical devices industry on February 5, a fund managed by global investment firm the Carlyle Group has completed the acquisition of Baxter International¡¯s Ren
Company
¡®Employees work long-term at Daiichi Sankyo for a reason'
by
Eo, Yun-Ho
Feb 13, 2025 05:58am
To survive and develop, we need to change and adapt to change. This is easy to say, but never easy to do. Daiichi Sankyo is a master of adaptation. The company has established itself in the domestic market by supplying drugs for chronic diseases, mainly cardiovascular diseases. Starting with hypertension drugs such as Olmetec, Sevikar, an
Product
Non-face-to-face treatment takes another hit
by
Jung, Heung-Jun
Feb 12, 2025 06:13am
Following the restriction of Wegovy prescriptions through non-face-to-face medical care, voices are rising on the need to regulate the prescription of artificial tears as well. The platform industry believes that overprescription is an issue that occurs regardless of whether the patient receives face-to-face or non-face-to-face care. The
Opinion
[Reporter's View] KRW 400m drug approval fee
by
Lee, Hye-Kyung
Feb 12, 2025 06:13am
Now, the new drug approval fee in South Korea costs KRW 410 million. On September 9th, 2024, the Ministry of Food and Drug Safety (MFDS) issued an administrative notice of 'Revision to the Regulation of Fees for Pharmaceutical Approval.' The revision specifies details of increasing the new drug approval fee to KRW 410 million and reducing th
Product
Wegovy outpatient prescriptions ¡é¡¦pharmacy burden¡è
by
Jung, Heung-Jun
Feb 12, 2025 06:13am
Wegovy, whose sales suffered due to inventory shortage in pharmacies, has now become an intractable inventory four months after its launch in Korea. Wegovy is a self-injectable drug that requires refrigeration and is a non-returnable product. Each unit costs tens of thousands of won, so pharmacies bear a heavy burden if it becomes a dead
Policy
P3T for Sanofi¡¯s Itepekimab in rhinosinusitis approved
by
Lee, Hye-Kyung
Feb 12, 2025 06:13am
Sanofi Aventis' biological drug 'Itepekimab' is entering Phase III trial in Korea to secure an indication for chronic rhinosinusitis following chronic obstructive pulmonary disease (COPD). On the 10th, the Ministry of Food and Drug Safety approved Sanofi¡¯s 52-week Phase III randomized, double-blind, placebo-controlled, parallel-group cli
Company
Will 'Verzenio' be reimb for early breast cancer in 2025?
by
Eo, Yun-Ho
Feb 12, 2025 06:13am
The industry eyes whether 'Verzenio,' with expanding reimbursement challenges, will obtain results this year. According to sources, Lilly Korea's CDK4/6 inhibitor Verzenio (abemaciclib) is expected to be considered for the upcoming Cancer Disease Review Committee (CDRC) of the Health Insurance Review and Assessment Service (HIRA) for its
Policy
Boryung¡¯s Lenvima generic approved in Korea
by
Lee, Hye-Kyung
Feb 11, 2025 06:03am
Boryung has received approval for a generic version of the liver cancer treatment 'Lenvima Cap (lenvatinib).' It received approval as an incrementally modified drug (new salt version) and added a 12 mg dose, which is not available with the original drug. The Ministry of Food and Drug Safety (MFDS) approved three items on the 6th, includin
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