Adcetris

Brentuximab vedotin · SEAGEN INC.
CANCER MEDICINE · PRESCRIPTION ONLY (USA)

Adcetris ingredients

Active ingredientStrength
Brentuximab Vedotin50 mg/10.5mL

What Adcetris is used for

The FDA lists the approved uses on the official label (below). In the EU, brentuximab vedotin is approved as Adcetris for:

Hodgkin lymphomaAdcetris is indicated for adult patients with previously untreated CD30+ Stage IV Hodgkin lymphoma (HL) in combination with doxorubicin, vinblastine and dacarbazine (AVD).Adcetris is indicated for adult patients with previously untreated CD30+ Stage IIB with risk factors, Stage III or Stage IV HL in combination with etoposide, cyclophosphamide, doxorubicin, dacarbazine, dexamethasone (BrECADD).Adcetris is indicated for the treatment of adult patients with CD30+ HL at increased risk of relapse or progression following autologous stem cell transplant (ASCT).Adcetris is indicated for the treatment of adult patients with relapsed or refractory CD30+ Hodgkin lymphoma (HL):- following ASCT, or- following at least two prior therapies when ASCT or multi-agent chemotherapy is not a treatment option.Systemic anaplastic large cell lymphomaAdcetris in combination with cyclophosphamid…

EU wording from the European Medicines Agency; US approved uses can differ.

Key facts

Brand
Adcetris
Generic name
Brentuximab vedotin
Made by
SEAGEN INC.
Forms
Injection, Powder, Lyophilized, For Solution
Given
Intravenous
Drug class
CD30-directed Immunoconjugate
FDA approval
Biologic licence (BLA) BLA125388
On the US market since
2011

Official information

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Adcetris?

Adcetris (Brentuximab vedotin) is a cancer medicine made by SEAGEN INC., approved by the US FDA.

What are the ingredients of Adcetris?

Adcetris contains Brentuximab Vedotin (50 mg/10.5mL).

Is Adcetris approved in Europe?

The same active substance is approved in the EU as Adcetris.

From the FDA National Drug Code directory (open.fda.gov, public domain) and the European Medicines Agency medicines list. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, USA

For information only, not medical advice. This page is a plain-language summary written from standard prescribing information and the public guides linked below. Brands sometimes change their formula, so always check the composition printed on the pack. Doses here are typical adult doses; yours may differ. Do not start, stop or change a medicine without your doctor or pharmacist, and keep all medicines away from children. In an emergency, call 112 (India) or your local emergency number.