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Mogamulizumab-Kpkc: uses, dosing, side effects & brands

Mogamulizumab-Kpkc is a medicine sold in the U.S. under one brand, for mycosis fungoides and sezary syndrome. Below: what the FDA label says, every product that contains it, what the pills look like, and its recall record.

By the pharmaranks editorial teamReviewed against the FDA (openFDA label, NDC Directory & Enforcement) sourcesUpdated Jul 24, 2026How we research

Key facts

Treats
Mycosis Fungoides and Sezary Syndrome
Available as
Injectable
Sold as
Poteligeo
Prescription?
Prescription only
Generic available?
Not in our catalog

How mogamulizumab-kpkc is dosed

From the FDA label for Poteligeo (application BLA761051). Other mogamulizumab-kpkc products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.

1 mg/kg as an intravenous infusion over at least 60 minutes on days 1, 8, 15, and 22 of the first 28-day cycle and on days 1 and 15 of each subsequent cycle ( 2 ). 2.1 Recommended Dosage The recommended dose of POTELIGEO is 1 mg/kg administered as an intravenous infusion over at least 60 minutes. Administer on days 1, 8, 15, and 22 of the first 28-day cycle, then on days 1 and 15 of each subsequent 28-day cycle until disease progression or unacceptable toxicity. Administer POTELIGEO within 2 days of the scheduled dose. If a dose is missed, administer the next dose as soon as possible and resume dosing schedule. Do not administer POTELIGEO subcutaneously or by rapid intravenous administration. Recommended Premedications Administer premedication with diphenhydramine and acetaminophen for the first POTELIGEO infusion. 2.2 Dose Modifications for Toxicity Dermatologic Toxicity Permanently discontinue POTELIGEO for life-threatening (Grade 4) rash or for any Stevens-Johnson syndrome (SJS) or toxic epidermal necrolysis (TEN) [ see Warnings and Precautions (5.1) ]. If SJS or TEN is suspected, stop POTELIGEO and do not resume unless SJS or TEN has been excluded and the cutaneous reaction has resolved to Grade 1 or less. If moderate or severe (Grades 2 or 3) rash occurs, interrupt POTELIGEO and administer at least 2 weeks of topical corticosteroids. If rash improves to Grade 1 or less,…

Mogamulizumab-Kpkc side effects

The following serious adverse reactions are discussed in greater detail in other sections of the labeling: Dermatologic Toxicity [ see Warnings and Precautions (5.1) ]. Infusion Reactions [ see Warnings and Precautions (5.2) ]. Infections [ see Warnings and Precautions (5.3) ]. Autoimmune Complications [ see Warnings and Precautions (5.4) ]. Complications of Allogeneic HSCT after POTELIGEO [ see Warnings and Precautions (5.5) ]. The most common adverse reactions (reported in ≥20% of patients) are rash, infusion related reactions, fatigue, diarrhea, musculoskeletal pain, and upper respiratory tract infection ( 6.1 ). To report SUSPECTED ADVERSE REACTIONS, contact Kyowa Kirin, Inc. at 1-844-768-3544 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . 6.1 Clinical Trial Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The data described below reflect exposure to POTELIGEO in Study 0761-010, a randomized, open-label, actively controlled clinical trial for adult patients with MF or SS who received at least one prior systemic therapy [ see Clinical Studies (14) ]. Of 370 patients treated, 184 (57% with MF, 43% with SS) received POTELIGEO as randomized treatment…

Who shouldn’t take mogamulizumab-kpkc

None. None ( 4 ).

Every mogamulizumab-kpkc product we track (1)

Same active ingredient — different manufacturer, form, price and FDA recall record. That last one is what our independent score measures.

Only one: Poteligeo.

What people report to the FDA about mogamulizumab-kpkc

The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 2 reports naming mogamulizumab-kpkc, and the FDA flagged 50% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:

  • acute kidney injury1 reports
  • anaphylactic reaction1 reports
  • blood pressure systolic decreased1 reports
  • bone marrow transplant1 reports
  • chest discomfort1 reports
  • drug intolerance1 reports
  • dyspnoea1 reports
  • electrocardiogram qrs complex shortened1 reports

Read these as a signal, not a rate. A report does not mean mogamulizumab-kpkc caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label section above.

Source: openFDA drug/event (FAERS), retrieved July 25, 2026.

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Frequently asked questions

What is mogamulizumab-kpkc?

Poteligeo (Mogamulizumab-Kpkc) is a medication used to treat Mycosis Fungoides, Sezary Syndrome.

Can you take mogamulizumab-kpkc with other medicines?

It depends on the medicine. We check it against the FDA labels rather than guessing: our interaction checker searches each drug's own label for the other and quotes what it says, naming the section it came from. Run mogamulizumab-kpkc against whatever else you take — and remember that a label not naming a drug is not the same as that combination being safe.

What forms does mogamulizumab-kpkc come in?

Across the brands we track, mogamulizumab-kpkc is currently marketed as injectable, per the FDA's National Drug Code Directory. Each form is dosed differently — follow the label for the exact product you were prescribed.

Is there a generic mogamulizumab-kpkc?

We do not currently list a generic-labelled mogamulizumab-kpkc product. That does not always mean none exists — it means none appears under a generic name in the FDA data we track. Ask your pharmacist.

Cite this page
APA
pharmaranks. (2026, July 24). Mogamulizumab-Kpkc: uses, dosing, side effects & brands. https://pharmaranks.com/drugs/mogamulizumab-kpkc
MLA
“Mogamulizumab-Kpkc: uses, dosing, side effects & brands.” pharmaranks, 24 July 2026, https://pharmaranks.com/drugs/mogamulizumab-kpkc.

We summarise public FDA and NIH sources — for a clinical claim, cite the primary source we link to as well.

Sources: FDA openFDA drug label, National Drug Code Directory, and Enforcement (recall) database. This page reproduces public FDA data and is not medical advice. Dosing is set by your prescriber.

Read the full FDA label for mogamulizumab-kpkc on DailyMed (NIH) ↗.