BGB-16673-304: Safety and Efficacy of BGB-16673 Compared to Pirtobrutinib in CLL or SLL - Clinical Trial

¿Cuál es el Propósito de este estudio?

The study has 4 parts: screening, taking the study drug, stopping the drug, and follow-up. You'll get tests like blood work, heart checks, and scans. You'll be randomly given one of two medicines: BGB-16673 or Pirtobrutinib, both taken once a day. After stopping the medicine, you'll return for a check-up in about a month. If your cancer hasn't gotten worse, you'll visit every 6 months. If it has, the study team will check on you by phone or email. The whole study may last about 3 years with around 13 visits.

¿Cuál es la Condición que se está estudiando?

Relapsed/Refractory Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL)

¿Quién puede participar en el Estudio?

Who can join the study:

- Adults with a type of blood cancer called CLL or SLL who need treatment.

- They must have had certain treatments before and still have signs of the disease.

Who cannot join the study:

- People with other serious blood cancers or brain problems.

- People who had certain types of transplants or treatments recently.

- People with serious allergies to the study medicine.

- People with infections or bleeding problems.

- People who had a stroke or brain bleeding in the last 6 months.

- People who take certain blood-thinning medicines or have HIV.

Grupo etario
Adultos

¿Qué Implica?

Doctors are doing a study to test two new medicines called BGB-16673 and Pirtobrutinib. They want to find out which one works better and is safer for people who have a type of blood cancer called CLL or SLL and have already had treatment before.

Detalles del Estudio

Título Completo
BeOne Medicines Ltd. / ?A Phase 3, Open-Label, Randomized Study to Evaluate the Safety and Efficacy of BGB-16673 Compared to Pirtobrutinib in Patients With Relapsed/Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma
Investigador Principal
Andrea Sitlinger, MD
Especialista en oncología hematológica
Número de Protocolo
IRB: PRO00118734
NCT: NCT06973187
Fase
Phase III
ClinicalTrials.gov
Estado de inscripción
Abierto para inscripción
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Contribuya a Duke Health