Kumaha Cina nuju ngembangkeun terapi T-Cell CAR?

Ngembangkeun terapi CAR T Cell di Cina
Jumlah uji coba terapi CAR-T di Cina ngaleuwihan anu di Amérika Serikat ku 2018 salaku hasil tina ékosistem anu maju ieu. Nepi ka Juni 2022, perusahaan Cina parantos ngalaksanakeun 342 uji klinis CAR-T. Malignancies tina garis keturunan B mangrupikeun manifestasi anu paling umum. Dua produk CAR-T gaduh aplikasi komérsial, Yescarta dina Juni 2021 sareng Relma-cel dina Séptémber 2021, diantara seueur calon ubar.

Bagikeun Post Ieu

2023 Maret: CAR-T-cell therapy is a novel and effective cancer treatment modality that has revolutionized the treatment of cancer, particularly blood cancers. This therapy achieves a therapeutic effect or cures disease by repairing or reconstructing genetic materials that have been damaged. Since Roseberg first isolated tumour-infiltrating lymphocytes (TILs) to treat melanoma in 1986, the development of modified T cell therapy has gained significant momentum. Since the FDA approved the first Terapi CAR-T, Kymriah, in 2017, the CAR-T market has grown rapidly. According to Frost & Sullivan, the global CAR-T market size is projected to increase from USD 10 million in 2017 to USD 1.08 billion in 2020, and then to USD 9.05 billion in 2025, with a compound annual growth rate (CAGR) of 55% from 2019 to 2025, making it the fastest-growing segment of the global cell and gene therapies (CGT) market.

CAR-T therapy is one of CGT therapy’s subsegments. On the basis of the origin of T cells, CAR-T therapy can be divided into two categories. Autologous CAR-T-cell therapy, which employs the patient’s own immune cells, and allogeneic CAR-T-cell therapy, which employs T cells from donor blood or occasionally umbilical cord blood,. The majority of CAR-T therapies are autologous CAR T-sél terapi, which typically involve the steps outlined below:

Anjeun panginten hoyong maca: Terapi Sél T T di Cina

1) Sél T dipanén tina getih periferal pasien;

2) Viral vectors such as AAV then modify T cells with CAR genes that are directed against a specific cell-surface protein on cancer cells;

3) The modified CAR-T cells population is expanded according to the patient’s weight;

4) The expanded CAR-T cells are then reinfused back into the patient. The entire manufacturing procedure lasts between one and three weeks and requires GMP compliance in an ultra-clean environment.

CAR-T therapy has reached a level of success that has never been seen before in treating B-cell cancers that are resistant to or refractory to chemotherapy, including R/R, B-ALL, NHL, and MM. The effectiveness of treating solid tumours is also currently under investigation. CD19-targeting and BCMA-targeting CAR-T therapies achieve the greatest clinical success among all CAR-T therapies. Four of the six CAR-T therapies approved by the FDA target CD19, while two target BCMA.

The most significant advantage over small and large molecule drugs is that patients can replace lifelong treatment of chronic disease with a limited number of doses, or even just one.

The United States pioneered the development of the CAR-T industry. However, by the middle of the 2010s, China had learned quickly and was catching up to the United States. Principally, the key drivers can be attributed to the Chinese government’s support for the development of a CGT ecosystem comprised of biotech companies, academics, healthcare providers, investors, and the government. Following the prioritization of biotechnology in the thirteenth five-year plan, the Chinese government emphasized its strategy to accelerate the innovation and development of biotech industries, including cell therapy. In addition, pertinent ministries have issued encouraging action regulations.

Saatos publikasi Pendapat Déwan Nagara ngeunaan Reformasi Sistem Evaluasi, Tinjauan, sareng Persetujuan Narkoba sareng Alat Médis di 2015, pasar modal ogé aktip. Dina laju pertumbuhan taunan sanyawa 45%, perusahaan terapi sél Cina ngumpulkeun dana kira-kira USD 2.4 milyar antara taun 2018 sareng 2021.

Anjeun panginten hoyong maca: Biaya terapi CAR T Cell di Cina

The number of CAR-T therapy trials in China surpassed those in the United States by 2018 as a result of this thriving ecosystem. As of June 2022, Chinese companies had conducted 342 clinical CAR-T trials. Malignancies in the B lineage were among the most prevalent manifestations. Two Mobil-T products have commercial applications: Yescarta in June 2021 and Relma-cel in September 2021, among numerous drug candidates.

Numutkeun kana Frost & Sullivan, pasar CAR-T domestik diperkirakeun ningkat tina CNY 0.2 milyar dina 2021 janten CNY 8 milyar dina 2025, teras janten CNY 28.9 milyar dina 2030, dina CAGR 45% ti 2022 dugi ka 2030. kanyataan yén pasar CAR-T Cina masih di infancy na, kakuatan nyetir mantap aya.

Although the two approved CAR-T products are from Sino-US joint ventures Fosun Kite and JW Terapeutics, domestic players have made breakthroughs and caught up to global players in recent years. Legend Biotech, IASO Biotherapeutics, and CARsgen Therapeutics all obtained NDA approval for their BCMA CAR-T products, establishing them as the leaders in BCMA CAR-T therapy. CD19 CAR-T products are a focus for Juventas Therapeutics, Gracell Biotechnologies, Hrain Biotechnology, ImunoPharm, Shanghai Cell Therapy Group, and numerous domestic companies. Juventas Therapeutics is the leader in Chinese CD19 Terapi CAR-T now that the NMPA has accepted its NDA for CNCT19. CARsgen Therapeutics is a global leader in solid tumours, and CT041 is the first CAR-T candidate for treating solid tumours to enter Phase II percobaan klinis. Bioheng Biotéh sareng BRL Biotéh (Cina: ) nyiptakeun pasar CAR-T alogén anyar.

Anjeun panginten hoyong maca: Terapi CAR T Cell pikeun sababaraha myeloma di Cina

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