Release date: 2024-08-14 10:52:22 Article From: Lucius Laos Recommended: 138
Pemigatinib leads to constitutive activation of FGFR by activating FGFR amplification and fusion, thereby inhibiting FGFR1-3 phosphorylation and signaling and decreasing cell viability.
In a phase II clinical trial called FIGHT-202, Pemigatinib was evaluated in 107 patients with locally advanced or metastatic cholangiocarcinoma who had previously undergone FGFR2 gene fusion or nonfusion reconstruction. The results showed that among patients treated with Pemigatinib, the objective response rate (ORR) reached 36%, with 2.8% achieving complete response and 33% achieving partial response. In addition, 63% of patients achieved remission at 6 months or more, and 18% maintained remission at 12 months or more.
Clinical studies have shown that the median overall survival (OS) of Pemigatinib is 21.1 months, which is more than 3-fold compared to the historical average survival of patients treated with second and third-line therapy in the past, which is 6-7 months.
Pemigatinib inhibits the growth and spread of tumor cells by inhibiting the phosphorylation and signaling processes of FGFR1-3 and blocking the constitutive activation of FGFR signaling caused by FGFR amplification and fusion. In clinical trials, patients treated with Pemigatinib showed a reduction in tumor volume.
Pemigatinib has a high disease control rate (DCR) of 82%, indicating that the drug has a significant effect in controlling disease progression.
Pemigatinib can significantly prolong the overall survival of patients and bring new hope for the treatment of cholangiocarcinoma patients.
Pemigatinib is the first FDA-approved targeted therapy for cholangiocarcinoma, bringing a new breakthrough in the treatment of cholangiocarcinoma. In the future, with further research on Pemigatinib and the accumulation of clinical application experience, the drug is expected to play a greater role in the treatment of cholangiocarcinoma.
In addition, Pemigatinib has also been in clinical trials in other types of tumors, such as bladder cancer, urothelial cancer, colorectal cancer, and myeloproliferative tumors, showing broad application prospects.
【Warm tips】When patients buy generic drugs, they should choose formal channels to ensure the quality and safety of the drugs. Avoid purchasing counterfeit products from informal sources.
Lung cancer is the most rapidly increasing malignant tumor with the fastest increasing morbidity and···【more】
Recommended:2012024-09-07
On November 14, 2024, the Committee for Medicinal Products for Human Use (CHMP) of the European Medi···【more】
Recommended:1582025-13-01
Recent advancements have reaffirmed the significance of liquid biopsy in the management of advanced ···【more】
Recommended:1562025-06-01
FDA Approves First Generic Version of Victoza (liraglutide injection)The U.S. Food and Drug Administ···【more】
Recommended:1712024-30-12
The new indication involves the treatment of adult patients with locally advanced, unresectable non-···【more】
Recommended:1612024-24-12
he U.S. Food and Drug Administration (FDA) has approved Crenessity (crinecerfont) for use in combina···【more】
Recommended:1462024-17-12
In the phase Ib/II multicenter pivotal FELIX study, the autologous 41BB-ζ anti-CD19 chimeric antigen···【more】
Recommended:1052024-13-12
On 25 July 2024, the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHM···【more】
Recommended:2482024-26-08
Lucius Pharmaceutical Co., Ltd., was established in 2020 in Vientiane, the capital of Laos. It aims to offer safe, effective, and affordable medicines globally. With a factory spanning 25,000 square meters, the company manufactures 200+ generic drugs in diverse therapeutic fields.
Address:No.26 Thongmang village, Xaythany district, Vientiane Capital, Laos
E-mail:laoslucius@gmail.com
Whatsapp: