Yondelis

trabectedin · Pharma Mar S.A.
AUTHORISED IN THE EU

What Yondelis is used for

Yondelis is indicated for the treatment of patients with advanced soft-tissue sarcoma, after failure of anthracyclines and ifosfamide, or who are unsuited to receive these agents. Efficacy data are based mainly on liposarcoma and leiomyosarcoma patients. Yondelis in combination with pegylated liposomal doxorubicin (PLD) is indicated for the treatment of patients with relapsed platinum-sensitive ovarian cancer.

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Yondelis
Active substance
trabectedin
Disease area
Ovarian Neoplasms; Sarcoma
Medicine group
Antineoplastic agents
ATC code
L01CX01
Marketing authorisation holder
Pharma Mar S.A.
Authorised in the EU since
2007

Official information

In the USA

Same active substance: Evdi, Yondelis

In India

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 Yondelis used for?

Yondelis is indicated for the treatment of patients with advanced soft-tissue sarcoma, after failure of anthracyclines and ifosfamide, or who are unsuited to receive these agents. Efficacy data are based mainly on liposarcoma and leiomyosarcoma patients. Yondelis in combination with pegylated liposomal doxorubicin (PLD) is indicated for the treatment of patients with relapsed platinum-sensitive ovarian cancer.

What is the active substance in Yondelis?

Yondelis contains trabectedin.

Who makes Yondelis?

The EU marketing authorisation holder is Pharma Mar S.A..

Source: European Medicines Agency medicines data (ema.europa.eu), reproduced with acknowledgement of the source. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, EU

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