Pomalidomide Combined With Obinutuzumab in the Treatment of Patients With Relapsed/Refractory Indolent Lymphoma

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorInstitute of Hematology & Blood Diseases Hospital, China

About this trial

To explore the maximum tolerated dose (MTD) of pomalidomide in combination with obinutuzumab in patients with relapsed/refractory indolent lymphomas (including follicular lymphoma, marginal zone lymphoma, and chronic lymphocytic leukemia/small lymphocytic lymphoma) treated with the pomalidomide plus obinutuzumab combination regimen, and to determine the recommended phase II dose (RP2D); concurrently evaluating the efficacy and safety of pomalidomide combined with obinutuzumab in patients with relapsed/refractory indolent lymphomas.

Eligibility criteria

Qualifiers

Age ≥18 years old, regardless of gender;

Histopathologically confirmed CD20+ indolent lymphoma (FL, MZL, or SLL), WHO grade 1-3a;.

Relapsed or refractory disease after at least one prior line of therapy;.

ECOG-PS 0-2;

Disqualifiers

Any other type of lymphoma, including Burkitt lymphoma;

The investigator confirms that the patient may progress to aggressive lymphoma.

Patients with contraindications or allergies to the investigational drug.

History of VTE or cerebral infarction prior to treatment;.

Trial design

Treatments tested in this trial

  • Induction therapy of GP(Pomalidomide+Obinutuzumab)
  • maintenance therapy of GP(Pomalidomide+Obinutuzumab)

Treatment groups

53 Participants
are divided into 1 treatment group

Locations

This trial has no locations