This promotional website is for UK Healthcare Professionals involved in the management of haematological malignancies. Adverse event reporting information can be found below.
VENCLYXTO (venetoclax) is licenced in the following indications for CLL:1
VENCLYXTO in combination with obinutuzumab (VEN+O) or ibrutinib (VEN +I) is indicated for the treatment of adult patients with previously untreated CLL
VENCLYXTO in combination with rituximab (VEN+R) is indicated for the treatment of adult patients with CLL who have received at least one prior therapy
VENCLYXTO is licensed as monotherapy (VEN mono) for the treatment of CLL:
- in the presence of del(17p) or TP53 mutations in adult patients who are unsuitable for, or have failed a BCRi
- in the absence of del(17p) or TP53 mutations in adult patients who have failed both chemoimmunotherapy and a BCRi.
BCRi, B-cell receptor pathway inhibitor; CLL, Chronic lymphocytic leukaemia; HCP, Healthcare professional; del(17p), 17p deletion; R/R, Relapsed/refractory; TP53, Tumour protein 53; VEN mono, VENCLYXTO monotherapy; VEN+O, VENCLYXTO and Obinutuzumab; VEN+R, VENCLYXTO and Rituximab.
References
- VENCLYXTO Summary of Product Characteristics.
You are advised to read the Prescribing Information and Summary of Product Characteristics to evaluate patient suitability for VENCLYXTO.
VENCLYXTO PRESCRIBING INFORMATION
By clicking the link above you will leave the AbbVie Pro website and be taken to the eMC PI portal website.
VENCLYXTO SUMMARY OF PRODUCT CHARACTERISTICS
UK-VNCCLL-250022. Date of preparation: January 2025.