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Summary

A Phase III, Randomized, Double-blind, Controlled Multicenter Study of Intravenous PI3K Inhibitor Copanlisib in Combination With Standard Immunochemotherapy Versus Standard Immunochemotherapy in Patients With Relapsed Indolent Non-Hodgkin’s Lymphoma (iNHL)

Acronym:

Chronos 4

ACTRN/NCT /ethics:

NCT02626455

Scientific title:

A Phase III, Randomized, Double-blind, Controlled Multicenter Study of Intravenous PI3K Inhibitor Copanlisib in Combination With Standard Immunochemotherapy Versus Standard Immunochemotherapy in Patients With Relapsed Indolent Non-Hodgkin’s Lymphoma (iNHL)

Sponsor / Cooperative group:

Bayer

Summary:

The purpose of this study is to assess whether copanlisib in combination with standard immunochemotherapy (rituximab in combination with bendamustine [R-B] and rituximab in combination with a 4 drug combination of cyclophosphamide, doxorubicin, incristine and prednisone/prednisolone [R-CHOP]) is effective and safe compared with placebo in combination with standard immunochemotherapy (R-B or R-CHOP) in patients with relapsed iNHL who have received at least one, but at most three, lines of treatment, including rituximab and alkylating agents.

Trial & Patient Characteristics

Cancer TypeLymphoma
Trial TypeTreatment
PhasePhase III
Age Range18+ years
SexBoth
Tumour Streamnon-Hodkin's Lymphoma
Cancer StageLocally Recurrent or Locally Advanced
Anticipated Start Date2016-01-06
Anticipated End Date2024-12-31

Participating Hospitals

HospitalAshford Cancer Centre Research
Clinical Trial CoordinatorSue Yeend
Emailsyeend@adelaidecancercentre.com.au
Phone08 8292 2240
Principal InvestigatorDr Nicholas Wickham
Recruitment StatusRecruiting