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Clinical Trials/NCT02045095
NCT02045095
Terminated
Phase 1

A Phase 1, Open-Label, Multicenter, Dose Escalation Study to Assess the Safety and Tolerability of MLN7243, an Inhibitor of Ubiquitin-Activating Enzyme (UAE), in Adult Patients With Advanced Solid Tumors

Millennium Pharmaceuticals, Inc.0 sites29 target enrollmentJanuary 31, 2014

Overview

Phase
Phase 1
Intervention
MLN7243
Conditions
Advanced Malignant Solid Tumors
Sponsor
Millennium Pharmaceuticals, Inc.
Enrollment
29
Primary Endpoint
Number of Participants With Vital Sign Related TEAEs by Preferred Term (PT)
Status
Terminated
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this study is to evaluate safety and tolerability (establish maximum tolerated dose [MTD], inform the recommended phase 2 dose [RP2D], and identify the dose-limiting toxicities [DLTs]) of MLN7243.

Detailed Description

This is a single arm Phase I study with multiple dosing cohorts as noted below: * Schedule A: MLN7243 1 mg * Schedule A: MLN7243 2 mg * Schedule A: MLN7243 4 mg * Schedule A: MLN7243 8 mg * Schedule A: MLN7243 12 mg * Schedule A: MLN7243 18 mg * Schedule A: MLN7243 Homozygous Mutant 4 mg

Registry
clinicaltrials.gov
Start Date
January 31, 2014
End Date
November 9, 2016
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Schedule A: MLN7243 1 mg

MLN7243 1 milligram (mg), infusion, intravenously over 10-minutes, on Days 1, 4, 8, and 11 followed by 10 days of rest in a 21-day treatment cycle for a maximum of 12 months, or until symptomatic deterioration or disease progression (PD) or discontinuation of study for another reason, or until study is stopped.

Intervention: MLN7243

Schedule A: MLN7243 2 mg

MLN7243 2 mg, infusion, intravenously over 10-minutes, on Days 1, 4, 8, and 11 followed by 10 days of rest in a 21-day treatment cycle for a maximum of 12 months, or until symptomatic deterioration or PD, or discontinuation of study for another reason, or until study is stopped.

Intervention: MLN7243

Schedule A: MLN7243 4 mg

MLN7243 4 mg, infusion, intravenously over 10-minutes, on Days 1, 4, 8, and 11 followed by 10 days of rest in a 21-day treatment cycle for a maximum of 12 months, or until symptomatic deterioration or PD or discontinuation of study for another reason, or until study is stopped.

Intervention: MLN7243

Schedule A: MLN7243 8 mg

MLN7243 8 mg, infusion, intravenously over 10-minutes, on Days 1, 4, 8, and 11 followed by 10 days of rest in a 21-day treatment cycle for a maximum of 12 months, or until symptomatic deterioration or PD or discontinuation of study for another reason, or until study is stopped.

Intervention: MLN7243

Schedule A: MLN7243 12 mg

MLN7243 12 mg, infusion, intravenously over 10-minutes, on Days 1, 4, 8, and 11 followed by 10 days of rest in a 21-day treatment cycle for a maximum of 12 months, or until symptomatic deterioration or PD or discontinuation of study for another reason, or until study is stopped.

Intervention: MLN7243

Schedule A: MLN7243 18 mg

MLN7243 18 mg, infusion, intravenously over 10-minutes, on Days 1, 4, 8, and 11 followed by 10 days of rest in a 21-day treatment cycle for a maximum of 12 months, or until symptomatic deterioration or PD or discontinuation of study for another reason, or until study is stopped.

Intervention: MLN7243

Schedule A: MLN7243 Homozygous Mutant 4 mg

MLN7243 homozygous mutant 4 mg, infusion, intravenously over 10-minutes, on Days 1, 4, 8, and 11 followed by 10 days of rest in a 21-day treatment cycle for a maximum of 12 months, or until symptomatic deterioration or PD or discontinuation of study for another reason, or until study is stopped.

Intervention: MLN7243

Outcomes

Primary Outcomes

Number of Participants With Vital Sign Related TEAEs by Preferred Term (PT)

Time Frame: Baseline up to 30 days after last dose of study drug (Cycle 10 Day 41)

Number of Participants With Laboratory Related TEAEs by System Organ Class (SOC)

Time Frame: Baseline up to 30 days after last dose of study drug (Cycle 10 Day 41)

Number of Participants With Clinically Significant Electrocardiogram (ECG) Abnormalities

Time Frame: Cycle 1 Day 1 up to Cycle 1 Day 11

Number of Participants With Clinically Significant Echocardiogram Abnormalities

Time Frame: Cycle 1 Day 2 up to 30 days after last dose of study drug (Cycle 10 Day 41)

Number of Participants With TEAEs Related to Tropinin I and T

Time Frame: Baseline up to 30 days after last dose of study drug (Cycle 10 Day 41)

Number of Participants Reporting One or More Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)

Time Frame: Baseline up to 30 days after last dose of study drug (Cycle 10 Day 41)

Secondary Outcomes

  • CL: Total Clearance After Intravenous Administration for TAK-243(Cycle 1 Day 1 pre-dose and at multiple time points (up to 48 hours) post-dose; Cycle 1 Day 11 pre-dose and at multiple time points (up to 72 hours) post-dose)
  • Change From Baseline in Immunohistochemistry (IHC) Biomarkers in Tumor Biopsies at Cycle 1 Day 12 (C1D12) as Assessed by Histological Score (H-score)(Baseline and Cycle 1 Day 12)
  • Change From Baseline in IHC Biomarkers in Tumor Biopsies at C1D12 as Assessed by Positive Index(Baseline and Cycle 1 Day 12)
  • Duration of Response(Baseline up to end of study (approximately 7 months))
  • AUClast: Area Under the Plasma Concentration-time Curve From Time 0 to the Time of the Last Quantifiable Concentration for TAK-243(Cycle 1 Day 1 pre-dose and at multiple time points (up to 48 hours) post-dose; Cycle 1 Day 11 pre-dose and at multiple time points (up to 72 hours) post-dose)
  • Aet: Amount of TAK-243 Excreted Unchanged in Urine(Cycle 1 Day 1; Cycle 1 Day 11)
  • AUCτ: Area Under the Plasma Concentration-time Curve Over the Dosing Interval for TAK-243(Cycle 1 Day 1 pre-dose and at multiple time points (up to 48 hours) post-dose; Cycle 1 Day 11 pre-dose and at multiple time points (up to 72 hours) post-dose)
  • AUC∞: Area Under the Plasma Concentration-time Curve From Time 0 to Infinity for TAK-243(Cycle 1 Day 1 pre-dose and at multiple time points (up to 48 hours) post-dose; Cycle 1 Day 11 pre-dose and at multiple time points (up to 72 hours) post-dose)
  • Vss: Volume of Distribution at Steady State for TAK-243(Cycle 1 Day 1 pre-dose and at multiple time points (up to 48 hours) post-dose; Cycle 1 Day 11 pre-dose and at multiple time points (up to 72 hours) post-dose)
  • Ceoi: Plasma Concentration at the End of Infusion for TAK-243(Cycle 1 Day 1 and 11: pre-infusion to end of infusion (up to 10 minutes))
  • Fet: Percentage of TAK-243 Excreted Unchanged in Urine(Cycle 1 Day 1; Cycle 1 Day 11)
  • Terminal Phase Elimination Half-life (T1/2) for TAK-243(Cycle 1 Day 1 pre-dose and at multiple time points (up to 48 hours) post-dose; Cycle 1 Day 11 pre-dose and at multiple time points (up to 72 hours) post-dose)
  • Percentage of Participants With Best Overall Response(Baseline up to end of study (approximately 7 months))

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