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Completed

NCT Number: NCT02342665

Japanese Phase Ib/II Copanlisib in Relapsed, Indolent B-cell NHL

The primary objective of this study is to assess the safety profile of copanlisib at the recommended dose (primary endpoint). The recommended dose of copanlisib for Japanese patients will be determined in the dose escalation/safety evaluation part.

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Nagoya, Aichi-ken, Japan

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically confirmed diagnosis of indolent B-cell NHL, with histological subtype limited to the following:

Follicular lymphoma (FL) grade 1-2-3a Small lymphocytic lymphoma (SLL) with absolute lymphocyte count < 5 x 109/L at the time of diagnosis and at study entry Lymphoplasmacytoid lymphoma/Waldenström macroglobulinemia (LPL/WM) Marginal zone lymphoma (MZL) (splenic, nodal, or extra-nodal)

  • Relapsed or refractory after ≥ 2 prior lines of therapy (refractory defined as not responding to a standard regimen or progressing within 6 months of the last course of a standard regimen). Patients must have previously received rituximab and alkylating agent(s).
  • Japanese patients ≥ 20 years of age
  • ECOG performance status ≤ 2 (Eastern Cooperative Oncology Group:ECOG)
  • Life expectancy of at least 3 months
  • Adequate bone marrow, liver and renal function as assessed within 7 days before starting study treatment
  • Left ventricular ejection fraction (LVEF) ≥ lower limit of normal (LLN) for the Institution
  • Availability of fresh or archival tumor tissue

Exclusion criteria

  • Uncontrolled hypertension (blood pressure ≥ 150/90 mmHg, defined as systolic blood pressure > 150 mmHg and/or diastolic blood pressure > 90 mmHg, despite optimal medical management)
  • Patients with evidence or history of bleeding diathesis. Any hemorrhage or bleeding event ≥ CTCAE Grade 3 (NCI-CTC version 4.0) within 4 weeks of start of study medication (CTCAE: Common Terminology Criteria for Adverse Events, NCI: National Cancer Institute).
  • History or concurrent condition of interstitial lung disease or severely impaired pulmonary function
  • Unresolved toxicity higher than CTCAE grade 1 attributed to any prior therapy/procedure excluding alopecia.
  • Prior treatment with PI3K inhibitors
  • Systemic corticosteroid therapy (ongoing)
  • Type I or II diabetes mellitus with HbA1c > 8.5% or fasting plasma glucose > 160 mg/dL at Screening
  • Known history of human immunodeficiency virus (HIV) infection.
  • Hepatitis B or C requiring treatment
  • Cytomegalovirus (CMV) PCR positive at baseline
  • Known lymphomatous involvement of the central nervous system

Treatment and study plan

Copanlisib (BAY80-6946)

Drug

Dosing is weekly for the first 3 weeks (on Days 1, 8, and 15) of a 28-day cycle, followed by a 1-week break (i.e., no infusion on Day 22).

Primary outcomes

  1. Number of participants with Adverse Events

    Time frame: Up to 18 months

  2. Intensity of AE

    Time frame: Up to 18 months

    The NCI Common Terminology Criteria for Adverse Events (CTCAE, Version 4.0) will be used to assess the intensity of AE

  3. Objective Tumor Response (OR)

    Time frame: Up to 18 Years

    OR: Best response rating of complete response or partial response according to the criteria defined in the Revised Response Criteria for Malignant Lymphoma(JClin Oncol.2007 Feb)

  4. Recommended dose determined in the dose escalation/safety evaluation

    Time frame: Up to 18 months

Sponsors and collaborators

Lead sponsor

Bayer

Industry

Registry information

Official study title

Open-label, Uncontrolled, Single-arm, Phase Ib/II Study of Intravenous Copanlisib in Japanese Patients With Indolent B-cell Non Hodgkin's Lymphomas Relapsed After or Refractory to Standard Therapy

Important dates

Study start
2015
Primary completion
2018
Study completion
2022
First posted
Jan 21, 2015
Registry last updated
Jan 20, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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