Overview

This trial is active, not recruiting.

Condition breast cancer
Treatments trastuzumab, hermyl 1401o trastuzumab, paclitaxel, docetaxel
Phase phase 3
Target HER2
Sponsor Mylan Inc.
Collaborator Mylan GmbH
Start date July 2012
End date March 2016
Trial size 600 participants
Trial identifier NCT02472964, 2011-001965-42, MYL-Her3001

Summary

A multicenter, double-blind, randomized, parallel-group, Phase III study of the efficacy and safety of Hercules( Myl 1401O, Mylan Trastuzumab) plus taxane versus Herceptin® plus taxane as first line therapy in patients with HER2-positive metastatic breast cancer.

United States No locations recruiting
Other countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification bio-equivalence study
Intervention model parallel assignment
Masking double blind (subject, caregiver, investigator, outcomes assessor)
Primary purpose treatment
Arm
(Active Comparator)
Part 1: Herceptin© (trastuzumab) intravenously+ paclitaxel 80 mg/m2 weekly intravenously or docetaxel 75 mg/m2 intravenously once every three weeks (investigators choice) for 8 cycles then evaluate for primary endpoint. Part 2: If SD or PR, CR at cycle 9 (week 24) proceed to Herceptin© (trastuzumab) alone once every 3 weeks until DP or subject withdrawal .
trastuzumab Herceptin©;
Trastuzumab 8mg/kg Iv over 90 minutes x 1 then Trastuzumab 6 mg/kg IV over 30 minutes every 3 weeks
paclitaxel
Paclitaxel 80mg/m2 IV over 60 minutes weekly.
docetaxel
Docetaxel 75mg/m2 IV over 60 minutes on day 1 of a 3 week cycle
(Experimental)
Part 1:Myl 1401OTrastuzumab Intravenously + paclitaxel 80 mg/m2 weekly intravenously or docetaxel 75 mg/m2 intravenously once every three weeks (investigators choice) for 8 cycles then evaluate for primary endpoint. Part 2: If SD or PR, CR at cycle 9 (week 24) proceed to Myl 1401O( Mylan Trastuzumab) alone once every 3 weeks until DP or subject withdrawal.
hermyl 1401o trastuzumab Hercules
HERMyl 1401O Trastuzumab 8mg/kg Iv over 90 minutes x 1 then HERMyl 1401O Trastuzumab 6 mg/kg IV over 30 minutes every 3 weeks
paclitaxel
Paclitaxel 80mg/m2 IV over 60 minutes weekly.
docetaxel
Docetaxel 75mg/m2 IV over 60 minutes on day 1 of a 3 week cycle

Primary Outcomes

Measure
compare best overall response rate (ORR) (according to Response Evaluation Criteria in Solid Tumor [RECIST] 1.1 criteria) at Week 24 with Hercules( Myl 1401O, Mylan Trastuzumab) in combination with taxane versus Herceptin® plus taxane
time frame: from time of First treatment to week 24

Secondary Outcomes

Measure
time to tumor progression (TTP);
time frame: from time of first treatment to week 24 at every 6 week intervals
•overall survival (OS)
time frame: from time of first treatment to week 24 at every 6 week intervals
duration of response (DR).
time frame: from time of first treatment to week 24 at every 6 week intervals

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria

  • Serum creatinine ≤1.5 x ULN (upper limit of normal),
  • Total bilirubin ≤1.0 x ULN (>1.0 x ULN if documented Gilbert's disease),
  • Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) ≤2.5 x ULN,
  • AST and/or ALT <1.5 x ULN if alkaline phosphatase >2.5 x ULN,
  • Alkaline phosphatase >2.5 x ULN;if bone metastases present and no liver dysfunction present. Left ventricular ejection fraction (LVEF) within institutional range of normal as measured by multiple gated acquisition scan or echocardiogram.

Exclusion Criteria

    Additional Information

    Official title A Multicenter, Double-Blind, Randomized, Parallel-Group, Phase III Study To Compare The Efficacy And Safety Of Hercules Versus Herceptin® In Patients With HER2+ Metastatic Breast Cancer
    Description Part 1: A multicenter, double-blind, randomized, parallel-group, Phase III study to compare the efficacy and safety of Hercules( Myl 1401O, Mylan Trastuzumab) plus taxane versus Herceptin® plus taxane in patients with HER2+ MBC. Either docetaxel or paclitaxel (Investigator site level choice) is planned for at least 24 weeks until documented response to therapy, disease progression, or discontinuation. Disease response and progression will be assessed locally by the Investigator on the basis of clinical and radiographic evidence using RECIST 1.1 criteria. The primary and secondary efficacy analyses will be performed using independently assessed radiographic evidence for the Intent-to-Treat (ITT) population. The primary analysis population for best ORR will be those patients who had measureable disease at baseline and for the secondary endpoint, DR, only those who are responders will be included in the analysis. Part 2: A multicenter, double-blind, parallel-group study to continue to compare the safety and immunogenicity and efficacy of Hercules( Myl 1401O, Mylan Trastuzumab) versus Herceptin® in patients with HER2+ MBC who have clinical benefit to first-line combination therapy with a taxane. All patients who have at least stable disease (SD), will continue with either single agent Hercules( Myl 1401O, Mylan Trastuzumab) or Herceptin® alone until death, unacceptable toxicity or disease progression. Population pharmacokinetics: During Part 1 of the study, for both the Hercules ( Myl 1401O, Mylan Trastuzumab)and Herceptin® treatment arms, PK sampling for Cmin and Cmax (end of infusion) will be collected for all patients. A PopPK subset, with sufficient samples available to perform the necessary analysis of PopPK modeling will be used to assess AUC, Cmax, Cmin, clearance, Vd, and T1/2 at various time points in the PopPK. Patients randomized into the main study will sign an additional consent form for the PopPK subset. We anticipate that approximately 80 patients will need to be enrolled in this subset collection in order to obtain sufficient samples for analysis. Long term survival follow-up: OS for this treated population will be determined with every 3 month follow-up until either 240 deaths or 36 months, whichever occurs first, as observed from the time of randomization. Exploratory evaluations: In addition, during Part 1 of the study, blood samples will be collected in all patients to assess the impact of soluble shed HER2/ECD on PK and efficacy at pre-dose on Cycles 1, 3, 5, 7, and end of treatment (EOT). Additional samples (ECD) will be obtained on Cycles 9, 13 and every 4 cycles thereafter, EOT and end of study (EOS) for continued evaluation of immunogenicity in patients continuing to receive therapy. A blood sample will be obtained on Cycle 1, Day 1, to be used for assay development and validation
    Trial information was received from ClinicalTrials.gov and was last updated in May 2016.
    Information provided to ClinicalTrials.gov by Mylan Inc..