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Phase 3 N=108 Randomized Quadruple-blind Treatment

Comparing Efficacy and Safety of AryoGen Pharmed Biosimilar Trastuzumab (AryoTrust) Versus Herceptin® in Breast Cancer

Malignant Neoplasm of Breast

Enrolled (actual)
108
Serious AEs
0.0%
Results posted
Jun 2024
Primary outcome: Primary: Pathologic Complete Response — 18; 15 Participants — p=0.73

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Trastuzumab plus docetaxel (for four 21-day cycles) after four 14-day cycles of Doxorubicin plus cyclophosphamide (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
AryoGen Pharmed Co.
Primary completion
Mar 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Pathologic Complete Response
18; 15 0.73
SECONDARY
Clinical Objective Response
41; 35 0.72
SECONDARY
Breast Conservation Rate
11; 7 0.42
SECONDARY
Safety Assessment by Evaluation of Adverse Events (AEs) and Abnormal Laboratory Results
54; 54 0.59
SECONDARY
The Number of Participants With Anti-drug Antibodies Against Trastuzumab (AryoTrust)
0; 0

Summary

This is A Phase III, randomized, two-armed, patient-outcome assessor-data analyzer blinded, parallel active controlled non-Inferiority clinical trial study to evaluate efficacy and safety of AryoTrust (Aryogen Trastuzumab in comparison to Herceptin® (Genentech/Roche) in patients with Human Epidermal Growth Factor Receptor 2-Positive breast cancer. The main objective is to verify the non-inferiority of AryoTrust (Aryogen trastuzumab) vs. Herceptin® (Genentech/Roche trastuzumab), both given concomitantly with docetaxel after doxorubicin plus cyclophosphamide in the neoadjuvant setting according to pathological complete response (pCR) as primary objective and objective response (cOR), clinical complete response (cCR), clinical partial response (cPR), clinical stable disease (cSD), clinical progressive disease (cPD), breast conservation rate as Secondary objectives of this study. Evaluating the safety and immunogenicity of AryoTrust vs. Herceptin®, are also the other secondary outcomes. This study has two arms and 108 subjects will participate with a 1:1 allocation and receive mentioned treatment randomly.

Eligibility Criteria

Inclusion Criteria

  • 18-70 years old female patients
  • Patients with newly diagnosed stage III (locally advanced) or inoperable stage II (due to sizes larger than 5 cm or high tumor to breast ratio) tumors are candidates for participation.
  • Willing and able to sign an informed consent
  • Pathological diagnosis of adenocarcinoma of the breast
  • ECOG status of 0-1
  • With any ER/PR status
  • HER2 positive (Immunohistochemical (IHC) 3+ intensity, amplification of the HER2 gene on fluorescence in situ hybridization (FISH+ ) or HER2 positive results of Chromogenic in situ hybridization (CISH+)).

Exclusion Criteria

  • Clinical or radiologic evidence of metastatic disease
  • History of any other malignancy including previous breast cancer, second non-breast malignant disease
  • History of previous chemotherapy
  • Left ventricular ejection fraction [LVEF] 100 mmHg or systolic > 200 mmHg), A severe conduction abnormality (having pacemaker or diagnosed by the ECG) and any other significant cardiovascular disease.
  • Hematologic abnormalities including baseline Absolute Neutrophil Count (ANC) of ≤1,500/µL or platelet count ≤ 100,000/µL
  • Liver dysfunction including : (baseline)
  • Alanine amino transferase (ALT) and/or aspartate amino transferase (AST) ≥ 3 Upper Limit Normal (ULN)
  • Alkaline phosphatase (ALP) ≥3 ͯ ULN
  • serum total bilirubin > 1.5 ULN
  • Renal dysfunction, defined as serum creatinine ≥2.5 mg/dL
  • Pregnant, lactating women or women of childbearing potential who are not willing to use adequate contraception
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03425656). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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