Padcev Ejfv

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

Padcev Ejfv ingredients

Active ingredientStrength
Enfortumab Vedotin30 mg/3mL, 20 mg/2mL

What Padcev Ejfv is used for

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

Muscle invasive bladder cancer (MIBC) Padcev, in combination with pembrolizumab, as neoadjuvant treatment and then continued after radical cystectomy as adjuvant treatment, is indicated for the treatment of adult patients with resectable muscle invasive bladder cancer (MIBC). Unresectable or metastatic urothelial cancer Padcev, in combination with pembrolizumab, is indicated for the first-line treatment of adult patients with unresectable or metastatic urothelial cancer who are eligible for platinum-containing chemotherapy. Locally advanced or metastatic urothelial cancer Padcev as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial cancer who have previously received a platinum-containing chemotherapy and a programmed death receptor‑1 or programmed death‑ligand 1 inhibitor (see section 5.1).

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

Key facts

Brand
Padcev Ejfv
Generic name
Enfortumab vedotin
Made by
SEAGEN INC.
Forms
Injection, Powder, Lyophilized, For Solution
Given
Intravenous
FDA approval
Biologic licence (BLA) BLA761137
On the US market since
2019

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 Padcev Ejfv?

Padcev Ejfv (Enfortumab vedotin) is a cancer medicine made by SEAGEN INC., approved by the US FDA.

What are the ingredients of Padcev Ejfv?

Padcev Ejfv contains Enfortumab Vedotin (30 mg/3mL, 20 mg/2mL).

Is Padcev Ejfv approved in Europe?

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

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.