Ixazomib Rollover Study

NCT02924272 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2025-03-12

Study results available
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Summary

The purpose of this study is to provide continued access to ixazomib and/or other study drugs from an ixazomib parent study.

Conditions

Interventions

DRUG

Ixazomib

Ixazomib Capsules

Sponsors & Collaborators

  • Takeda Development Center Americas, Inc.

    collaborator INDUSTRY
  • Takeda

    lead INDUSTRY

Principal Investigators

  • Medical Director · Takeda

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-12-16
Primary Completion
2024-07-03
Completion
2024-07-03
FDA Drug
Yes

Countries

  • United States
  • Belgium
  • Canada
  • China
  • Greece
  • Japan
  • Poland
  • Singapore
  • South Korea
  • Spain
  • Sweden

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02924272 on ClinicalTrials.gov