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Clinical Trial Summary

Polatuzumab, bendamustine and rituximab in patients with relapsed/ refractory mantle cell lymphoma


Clinical Trial Description

Polatuzumab vedotin will be administered at a dose of 1.8 mg/kg i.v. on day 2 of cycle 1, then on day 1 of each subsequent cycle. Bendamustine will be administered at a dose 90 mg/m2 i.v. day 2 & 3 of cycle 1, then on day 1 & 2 of each subsequent cycle. Rituximab will be administered at a dose 375 mg/m2 i.v. on day 1 of each cycle. Each cycle is 21 days long Response rate by RECIST 1.1 is definied as the primary study endpoint. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05868395
Study type Interventional
Source Medical University of Vienna
Contact Barbara Kiesewetter, MD
Phone +43140400
Email barbara.kiesewetter@meduniwien.ac.at
Status Recruiting
Phase Phase 2
Start date January 2, 2024
Completion date May 24, 2027

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