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Multicentre Registry of Treatments and Outcomes in Patients With Chronic Lymphocytic Leukaemia (CLL) Or Indolent Non Hodgkin's Lymphoma (iNHL) (NADIR)

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Astellas

Status

Terminated

Conditions

Chronic Lymphocytic Leukaemia (CLL)
Indolent Non Hodgkin's Lymphoma (iNHL)

Study type

Observational

Funder types

Industry

Identifiers

NCT02273856
ONC-MA-1002

Details and patient eligibility

About

The purpose of this study is to document the pharmacological treatment strategies used in treatment naïve and previously treated relapsed/refractory iNHL/CLL patients in the Middle East and North African (MENA) region. This study will also record encountered tumor subtype and stage and the instituted pharmacological treatments, as well as assess the clinical outcomes of treatments.

Full description

Patients will be followed up to 30 months.

Enrollment

25 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Informed consent
  • CLL patients or
  • iNHL patients
  • Clinical decision made to initiate or adapt treatment of CLL/iNHL("Need to treat")

Exclusion criteria

  • Patient deemed unfit for enrollment by the documented opinion of the investigator
  • Watch and wait patients
  • Richter's transformation
  • Patients otherwise not eligible for (pharmacological) intervention
  • Moribund patients

Trial design

25 participants in 4 patient groups

Treatment naïve patients with CLL
Treatment naïve patients with iNHL
Relapsed/refractory patients with CLL
Relapsed/refractory patients with iNHL

Trial contacts and locations

8

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Data sourced from clinicaltrials.gov

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