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Venclyxto (venetoclax)

Region

🇪🇺 EU

Active substance

venetoclax

Company

AbbVie Deutschland GmbH & Co. KG

Status

Authorised

Therapeutic area

Leukemia, Lymphocytic, Chronic, B-Cell

EU approval

Sun 04 Dec 2016

Application

EMEA/H/C/004106

ATC

L01XX52

Official record

www.ema.europa.eu

Indication

Venclyxto is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (CLL): in combination with acalabrutinib with or without obinutuzumab  in combination with obinutuzumab in combination with ibrutinib   Venclyxto in combination with rituximab is indicated for the treatment of adult patients with CLL who have received at least one prior therapy.   Venclyxto monotherapy is indicated for the treatment of CLL: in the presence of 17p deletion or TP53 mutation in adult patients who are unsuitable for or have failed a B cell receptor pathway inhibitor, or in the absence of 17p deletion or TP53 mutation in adult patients who have failed both chemoimmunotherapy and a B cell receptor pathway inhibitor.   Venclyxto in combination with a hypomethylating agent is indicated for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (AML) who are ineligible for intensive chemotherapy.

Regulatory milestones

No milestones recorded in the last year.

Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.