Study of Inotuzumab Ozogamicin + Temsirolimus in Patients With Relapsed or Refractory CD22+ B-cell NHLymphoma (IOSI-LND-001)

Cristiana Sessa

Status and phase

Completed

Phase 1

Conditions

B-cell Lymphoma Refractory

Treatments

Drug: Inotuzumab Ozogamicin

Drug: Temsirolimus

Study type

Interventional

Funder types

Other

Identifiers

NCT01535989

IOSI-LND-001

Details and patient eligibility

About

This is an open label phase I study of Inotuzumab Ozogamicin, an antibody-targeted intravenous chemotherapy agent composed of a CD22-targeted antibody linked to calicheamicin, in combination with the mammalian target of rapamycin (mTOR) inhibitor Temsirolimus, in patients with relapsed/refractory CD22+ B-cell non Hodgkin's lymphomas (NHLs). Both Inotuzumab Ozogamicin and Temsirolimus have been evaluated as single agents as well as in combination with rituximab in patients with NHLs. This is the first study combining the two agents together. In the present study Inotuzumab Ozogamicin will be administered intravenously on d1 at the starting dose of 0.8 /m2. Temsirolimus will be administered intravenously on days 1,8,15 and 22 at the starting dose of 15mg. Cycles will be repeated every 28 days.

Enrollment

25 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Key inclusion criteria

Histologically and/or cytologically confirmed relapsed or refractory CD22+ B-cell Non Hodgkin's Lymphomas
No limitations on prior treatments. Patients must have progressed after at least one prior therapy.
Adult patients (aged > 18yrs old).
ECOG status ≤ 1.
Life expectancy greater than 3 months.
Adequate organ and marrow function.

Key exclusion criteria