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Etuvetidigene autotemcel

Etuvetidigene autotemcel is a medicine in the class miscellaneous.

  • 藥物類別: Miscellaneous

最後更新 來源: US FDA label

僅供醫療專業人員參考。本頁為簡要摘要,並非醫療建議,亦不能取代官方仿單或臨床判斷。開立處方或調劑前請務必核實。

本頁的臨床內容僅提供英文版。

重點資訊

藥物類別
Miscellaneous
常見劑型
注射劑
商品名
1
國家與市場
1

劑型、規格與商品名稱會因國家而異。請核對您手上的產品。

作用方式

Adds full-length copies of the human WAS cDNA into the patient's hematopoietic stem cells by lentiviral vector transduction. After infusion the modified cells engraft in bone marrow and repopulate the hematopoietic compartment, and their progeny express WAS protein (WASP).

成人常用劑量(仿單摘要)

Wiskott-Aldrich Syndrome: minimum recommended dose 7 × 10 6 CD34 + cells/kg based on body weight at infusion, single-dose intravenous infusion via central venous catheter; maximum volume must remain < 20% of estimated plasma volume

僅摘錄仿單中第一行劑量說明;完整的劑量內容請見 App。

懷孕與哺乳

懷孕
Unsafe One-time gene therapy (own modified stem cells). No data in pregnancy. It must not be given during pregnancy because of the risks of the conditioning chemotherapy. Confirm a negative pregnancy test first; use contraception from stem-cell collection until at least 6 months after the infusion.
哺乳
Unsafe No data on presence in milk. Nearly all patients are boys (X-linked disease). Because of the risks of conditioning chemotherapy, breastfeeding must stop during conditioning; afterwards follow the advice for the conditioning drugs.

已通報的副作用

  • Catheter related infection
  • Bacterial and viral infections
  • Diarrhea
  • Vomiting
  • Stomatitis
  • Liver injury

禁忌症

  • Hypersensitivity to the active substance or to any of the excipients
  • Previous HSCT within 6 months prior to treatment, or HSCT with evidence of residual donor cells
  • Previous treatment with hematopoietic stem cell gene therapy

哪些人需要特別留意

  • Hypersensitivity and infusion-related reactions, including anaphylaxis, may occur due to DMSO; monitor during and after infusion
  • Engraftment failure may occur; if so, infuse non-transduced back-up stem cells
  • Severe cytopenias occur for several weeks; monitor for at least 8 weeks

請告知藥師或醫師您是否懷孕或哺乳、是否患有腎臟或肝臟疾病、是否有過敏,以及您正在使用的所有其他藥物或保健品。

Pro+ 會員專屬

解鎖完整頁面

建立帳號並開始 Pro+ 試用,即可開啟 Etuvetidigene autotemcel 的完整藥品專論:劑量、懷孕與哺乳、副作用、警示及所有交互作用。

  • Dosing by age, kidney and liver function, and further dose lines
  • Paediatric dosing
  • How to give it
  • Patient counselling points
  • IV preparation and dilution

在網頁版免費試用 Pro+ 14 天,無需信用卡。

同類別的其他藥品

常見問題

What is Etuvetidigene autotemcel used for?

Etuvetidigene autotemcel is a medicine in the class miscellaneous.

What side effects have been reported with Etuvetidigene autotemcel?

Catheter related infection, Bacterial and viral infections, Diarrhea, Vomiting, Stomatitis, Liver injury.

Can Etuvetidigene autotemcel be taken in pregnancy or while breastfeeding?

Pregnancy: Unsafe. One-time gene therapy (own modified stem cells). No data in pregnancy. It must not be given during pregnancy because of the risks of the conditioning chemotherapy. Confirm a negative pregnancy test first; use contraception from stem-cell collection until at least 6 months after the infusion. Breastfeeding: Unsafe. No data on presence in milk. Nearly all patients are boys (X-linked disease). Because of the risks of conditioning chemotherapy, breastfeeding must stop during conditioning; afterwards follow the advice for the conditioning drugs.

What does Etuvetidigene autotemcel interact with?

MediHelp does not list a checked interaction for Etuvetidigene autotemcel yet. Always tell your pharmacist about every medicine you take.

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