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Clinical Trials/NCT02514239
NCT02514239
Completed
Phase 1

An Open Label, Phase I, Dose Escalation Study to Characterize the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intravenous Doses of BI 836909 in Relapsed and/or Refractory Multiple Myeloma Patients

Boehringer Ingelheim5 sites in 2 countries43 target enrollmentJuly 8, 2015
InterventionsBI 836909

Overview

Phase
Phase 1
Intervention
BI 836909
Conditions
Multiple Myeloma
Sponsor
Boehringer Ingelheim
Enrollment
43
Locations
5
Primary Endpoint
The Maximum Tolerated Dose (MTD) of BI 836909
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The primary objective of this trial is to determine the maximum tolerated dose (MTD) of BI 836909 administered by continuous i.v. infusion in patients with relapsed and/or refractory multiple myeloma. If the MTD is not reached based on safety findings, a recommended dose for further development will be determined. This will depend on the safety data, pharmacokinetic/pharmacodynamics data and potentially preliminary efficacy data. Secondary objectives are to document the safety and tolerability of BI 836909, to perform pharmacokinetic and pharmacodynamic analyses and to evaluate relevant biological effects in terms of parameters of efficacy.

Registry
clinicaltrials.gov
Start Date
July 8, 2015
End Date
July 2, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Intravenous Infusion of BI 836909 (0.2 μg/d)

Intervention: BI 836909

Intravenous Infusion of BI 836909 (0.4 μg/d)

Intervention: BI 836909

Intravenous Infusion of BI 836909 (0.8 μg/d)

Intervention: BI 836909

Intravenous Infusion of BI 836909 (1.6 μg/d)

Intervention: BI 836909

Intravenous Infusion of BI 836909 (3.2 μg/d)

Intervention: BI 836909

Intravenous Infusion of BI 836909 (6.5 μg/d)

Intervention: BI 836909

Intravenous Infusion of BI 836909 (13 μg/d)

Intervention: BI 836909

Intravenous Infusion of BI 836909 (25 μg/d)

Intervention: BI 836909

Intravenous Infusion of BI 836909 (50 μg/d)

Intervention: BI 836909

Intravenous Infusion of BI 836909 (100 μg/d)

Intervention: BI 836909

Intravenous Infusion of BI 836909 (200 μg/d)

Intervention: BI 836909

Intravenous Infusion of BI 836909 (400 μg/d)

Intervention: BI 836909

Intravenous Infusion of BI 836909 (800 μg/d)

Intervention: BI 836909

Outcomes

Primary Outcomes

The Maximum Tolerated Dose (MTD) of BI 836909

Time Frame: Cycle 1, up to 6 weeks.

The Maximum tolerated dose (MTD) of BI 836909, which was defined as the highest dose of the dose level tested where ≤1 patient out of 6 developed a Dose-limiting toxicity (DLT). The MTD was defined based on DLTs observed during Cycle 1. However, all Adverse Events corresponding to the definition of a DLT (see below) were to be considered for confirming the MTD. A DLT was defined as any drug-related non-haematological Adverse Event of Common Terminology Criteria for Adverse Events (CTCAE) version 4.03 Grade 3 or higher.

The Number of Patients With Dose-limiting Toxicities (DLTs)

Time Frame: Cycle 1, up to 6 weeks.

The number of patients with Dose-limiting toxicities (DLTs) in cycle 1. A Dose-limiting toxicity was defined as any drug-related non-haematological Adverse Event of Common Terminology Criteria for Adverse Events (CTCAE) version 4.03 Grade 3 or higher.

Secondary Outcomes

  • Number of Participants With an Objective Response(On-treatment: From start of treatment till end of trial (EOT) visit, up to 61 weeks. Extended follow-up: From start of treatment till the last extended follow-up visit which was scheduled at 12 months after end of treatment, up to 113 weeks.)
  • Duration of Objective Response - on Treatment(From start of treatment till end of trial (EOT) visit, up to 61 weeks.)
  • Duration of Objective Response - Including Extended Follow up Visits(From start of treatment till the last extended follow-up visit which is scheduled at 12 months after end of treatment, up to 113 weeks.)
  • Number of Participants With a Minimal Residual Disease (MRD) Response(On-treatment: From start of treatment till end of trial (EOT) visit, up to 61 weeks. Follow-up: From start of treatment till the last extended follow-up visit which was scheduled at 12 months after end of treatment, up to 113 weeks.)
  • Duration of Minimal Residual Disease (MRD) Response - on Treatment(From start of treatment till end of trial (EOT) visit, up to 61 weeks.)
  • Duration of Minimal Residual Disease (MRD) Response - Including Extended Follow up Visits(From start of treatment till the last extended follow-up visit which was scheduled at 12 months after end of treatment, up to 113 weeks.)
  • Progression-free Survival (PFS) - on Treatment(From start of treatment till end of trial (EOT) visit, up to 61 weeks.)
  • Progression-free Survival (PFS) - Including Extended Follow up Visits(From start of treatment till the last extended follow-up visit which was scheduled at 12 months after end of treatment, up to 113 weeks.)
  • Serum Concentration at Steady State of BI 836909 (Css)(Pharmacokinetic samples were collected at 48:00 hours (h):minutes (min), 168:00, 336:00, 504:00 and 671:50 h after the start of infusion of BI 836909 of the first cycle.)

Study Sites (5)

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