denileukin diftitox

{{Short description|Pharmaceutical drug}}

{{Use dmy dates|date=August 2024}}

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{{Infobox drug

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| verifiedrevid = 477002950

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| tradename = Ontak, others

| Drugs.com = {{drugs.com|monograph|denileukin_diftitox}}

| MedlinePlus = a611024

| DailyMedID = Denileukin diftitox

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| routes_of_administration = Intravenous

| class = Antineoplastic

| ATC_prefix = L01

| ATC_suffix = XX29

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| legal_US = Rx-only

| legal_US_comment = {{cite web | title=Ontak (denileukin diftitox) Injection for intravenous infusion Initial U.S. Approval: 1999 | website=DailyMed | url=https://dailymed.nlm.nih.gov/dailymed/archives/fdaDrugInfo.cfm?archiveid=246788 | access-date=9 August 2024}}https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/761312s000lbl.pdf

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| elimination_half-life = 70-80 min

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| CAS_number_Ref = {{cascite|correct|??}}

| CAS_number = 173146-27-5

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| IUPHAR_ligand = 7044

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| DrugBank = DB00004

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| UNII_Ref = {{fdacite|changed|FDA}}

| UNII = 25E79B5CTM

| KEGG = D03682

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| ChEMBL = 1201550

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| IUPAC_name = Diphtheria toxin-Interleukin-2 fusion protein

| C=2560 | H=4042 | N=678 | O=799 | S=17

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Denileukin diftitox, sold under the brand name Ontak among others, is an anti-cancer medication used for the treatment of adults with T-cell lymphoma. It is an IL2-receptor-directed cytotoxin. It is an engineered protein combining interleukin-2 and diphtheria toxin.{{cite journal | vauthors = Turturro F | title = Denileukin diftitox: a biotherapeutic paradigm shift in the treatment of lymphoid-derived disorders | journal = Expert Review of Anticancer Therapy | volume = 7 | issue = 1 | pages = 11–7 | date = January 2007 | pmid = 17187516 | doi = 10.1586/14737140.7.1.11 | s2cid = 9028829 }}

Medical uses

Denileukin diftitox is indicated for the treatment of adults with relapsed or refractory stage I-III cutaneous T-cell lymphoma after at least one prior systemic therapy.

Adverse effects

The prescription label contains a boxed warning that capillary leak syndrome (CLS), including life-threatening or fatal reactions, can occur in people receiving denileukin diftitox.

Society and culture

= Legal status =

In 1999, denileukin diftitox was approved by the US Food and Drug Administration (FDA) for the treatment of cutaneous T-cell lymphoma.{{cite journal | vauthors = Manoukian G, Hagemeister F | title = Denileukin diftitox: a novel immunotoxin | journal = Expert Opinion on Biological Therapy | volume = 9 | issue = 11 | pages = 1445–51 | date = November 2009 | pmid = 19817678 | doi = 10.1517/14712590903348135 | s2cid = 23956460 }}

References

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