Donislecel

Last updated

Donislecel
Clinical data
Trade names Lantidra
Other namesdonislecel-jujn
License data
Routes of
administration
Islet cell transplantation via intravenous infusion [1] [2]
ATC code
  • None
Legal status
Legal status
Identifiers
KEGG

Donislecel, sold under the brand name Lantidra, is a cellular therapy medication used for the treatment of type 1 diabetes. [3] [5] Donislecel is an allogeneic (donor) pancreatic islet cellular therapy made from deceased donor pancreatic cells. [5] Donislecel is administered as a single infusion into the hepatic (liver) portal vein. [5]

Contents

The most common adverse reactions include nausea, fatigue, anemia, diarrhea, and abdominal pain. [5]

Donislecel was approved for medical use in the United States in June 2023. [3] [5]

Medical uses

Donislecel is indicated for the treatment of adults with type 1 diabetes who are unable to approach target glycated hemoglobin (average blood glucose levels) because of current repeated episodes of severe hypoglycemia (low blood sugar) despite intensive diabetes management and education. [3] [5]

The primary mechanism of action of donislecel is believed to be the secretion of insulin by the infused allogeneic islet beta cells. [5] In some people with type 1 diabetes, these infused cells can produce enough insulin, so the recipient no longer needs to take insulin (by injections or pump) to control their blood sugar levels. [5]

Adverse effects

The most common adverse reactions include nausea, fatigue, anemia, diarrhea, and abdominal pain. [5]

History

The safety and effectiveness of donislecel was evaluated in two non-randomized, single-arm studies in which a total of 30 participants with type 1 diabetes and hypoglycemic unawareness received at least one infusion and a maximum of three infusions. [5] Overall, 21 participants did not need to take insulin for a year or more, with eleven participants not needing insulin for one to five years and ten participants not needing insulin for more than five years. [5] Five participants did not achieve any days of insulin independence. [5]

The FDA granted marketing approval of Lantidra to CellTrans, Inc. [5]

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References

  1. "Archived copy". Food and Drug Administration . Archived from the original on 9 December 2022. Retrieved 29 June 2023.{{cite web}}: CS1 maint: archived copy as title (link)
  2. "Archived copy". Food and Drug Administration . Archived from the original on 19 May 2021. Retrieved 29 June 2023.{{cite web}}: CS1 maint: archived copy as title (link)
  3. 1 2 3 4 "Lantidra- donislecel solution". DailyMed. 10 July 2023. Retrieved 28 August 2023.
  4. "Lantidra". U.S. Food and Drug Administration (FDA). 28 June 2023. Archived from the original on 5 July 2023. Retrieved 5 July 2023.
  5. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 "FDA Approves First Cellular Therapy to Treat Patients with Type 1 Diabetes". U.S. Food and Drug Administration (FDA) (Press release). 28 June 2023. Retrieved 28 June 2023.PD-icon.svg This article incorporates text from this source, which is in the public domain .

PD-icon.svg This article incorporates public domain material from the United States Department of Health and Human Services.