Name No. For Patients with Purpose
CLL17 20-22

Previously untreated Chronic Lymphocytic Leukaemia (CLL)

This trial will compare the efficacy of continuous ibrutinib monotherapy with fixed-duration venetoclax plus obinutuzumab and fixed-duration ibrutinib plus venetoclax in patients with previously untreated CLL


Name No. For Patients with Purpose
MO40598 CTRIAL-IE 18-47


This study will evaluate the safety and efficacy of Polatuzumab Vedotin (Pola) in combination with Mabthera plus Gemcitabine plus Oxaliplatin (R-GemOx) versus R-GemOx


Name No. For Patients with Purpose

Primary Myelofibrosis, Post-PV or Post-ET Myelofibrosis

This study will assess the efficacy and safety of fedratinib compared to best available therapy.

CALLS (INCB 84344-401)

Name No. For Patients with Purpose
CALLS (INCB 84344-401) 18-48

Participants with Chronic Myeloid Leukaemia (CML) and Philadelphia-positive Acute Lymphoid Leukaemia (Ph+ALL) who are being treated with their first or subsequent tyrosine kinase inhibitor (TKI) therapy.

The purpose of this observational study is to evaluate the prevalence of mutations in patients with Chronic Myeloid Leukaemia (CML) who meet the European Leukaemia Net (ELN) criteria for warning or failure and patients with Philadelphia-positive Acute Lymphoid Leukaemia (Ph+ALL) with detectable BCR-ABL currently being treated with first or subsequent Tyrosine Kinase Inhibitor (TKI) therapy in the UK, Ireland, or France using Next-Generation Sequencing.

Paradigme (LYMRIT-37-01)

Name No. For Patients with Purpose
Paradigme (LYMRIT-37-01) 18-15

Follicular Lymphoma that did not respond to treatment or recurred after chemotherapy or immunotherapy treatment.

To investigate the efficacy and safety of a new drug called Betalutin®. One dose of Betalutin® is given to patients. Betalutin® is an antibody which targets a protein on lymphoma cancer cells together with radioactivity to kill the cancer cells. Two doses of Betalutin® are used in this clinical trial and all patients receive Betalutin®. Patients will be requested to return to clinic for up to 5 years to have their cancer assessed and to collect any side effects.

CheckMate 744

Name No. For Patients with Purpose
CheckMate 744 17-07

Children, adolescents, and young adults with Classic Hodgkin Lymphoma whose disease has come back or did not respond to initial treatment.

The purpose of this study is to determine whether certain drug combinations are safe and effective.