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A Study to Assess the Bioequivalence of Trastuzumab Via Different Subcutaneous Delivery Platforms in Healthy Male Participants

A Study to Assess the Bioequivalence of Trastuzumab Via Different Subcutaneous Delivery Platforms in Healthy Male Participants

Recruiting
18-50 years
Male
Phase 1

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Overview

This two-part study will evaluate the bioequivalence, safety, and tolerability of a single SC dose of trastuzumab administered via handheld syringe/syringe pump (HHS/SP) with infusion set (IS) and an on-body delivery system (OBDS).

Eligibility

Inclusion Criteria:

  • Within body mass index (BMI) range 18 to 38 kilogram per meter square (kg/m2), inclusive. Body weight \<=100 kg
  • Left ventricular ejection fraction (LVEF) \>= 55 percent (%) measured by echocardiogram (ECHO)
  • Negative test result for drugs of abuse
  • Negative test result for hepatitis B surface antigen, hepatitis C virus (HCV), or human immunodeficiency virus (HIV) antibody screen
  • Negative test for latent Tuberculosis (TB) infection by QuantiFERON® TB Gold
  • Agree to use contraception and will refrain from sperm donation

Exclusion Criteria:

  • Significant history or clinical manifestation of any metabolic, allergic, dermatological, hepatic, renal, hematological, pulmonary, cardiovascular, respiratory, gastrointestinal, immunological, neurological, or psychiatric disorder; acute infection; or other unstable medical disease
  • History of moderate or severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric, human, or humanized antibodies or fusion proteins
  • Known sensitivity to recombinant hyaluronidase or other form of hyaluronidase
  • History or presence of atrial fibrillation
  • History of any clinically significant or clinically relevant cardiac condition
  • History or presence of clinically significant electrocardiogram (ECG) abnormalities
  • History of uncontrolled hypertension, hyperlipidemia, thyroid disorder, or diabetes
  • Family history of clinically significant and clinically relevant hypersensitivity, allergy, or severe cardiac diseases
  • History of previous anti-cancer treatments including pertuzumab, trastuzumab, anthracyclines, or any cardiotoxic drugs
  • History of active or latent TB, regardless of treatment history
  • Poor peripheral venous access
  • History or presence of any malignancy, with the exception of completely excised basal cell or squamous cell carcinoma of the skin

Study details
    Healthy Participants

NCT07214766

Genentech, Inc.

1 February 2026

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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