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ACTIVE NOT RECRUITING Phase 1

A Study of Runimotamab in Participants With Locally Advanced or Metastatic HER2-Expressing Cancers

NCT03448042 · View on ClinicalTrials.gov ↗

Study Summary

This study will evaluate the safety, tolerability, and pharmacokinetics of Runimotamab administered intravenously as a single agent and in combination with Trastuzumab in participants with locally advanced or metastatic Human Epidermal Growth Factor Receptor 2 (HER2)-expressing cancers.

Conditions Studied

Interventions

  • DRUG Trastuzumab
  • DRUG Tocilizumab
  • DRUG Runimotamab

Study Locations (20)

Other

  • Grand Hopital de Charleroi asbl — Charleroi
  • Rigshospitalet-Blegdamsvej 9 — Copenhagen
  • Institut Claudius Regaud — Toulouse
  • National Cancer Center East — Chiba
  • Het Nederlands Kanker Instituut Antoni Van Leeuwenhoek Ziekenhuis — Amsterdam
  • National Cancer Centre — Singapore
  • Asan Medical Center — Seoul
  • Seoul National University Hospital — Seoul

Connecticut

  • Yale University — New Haven

Michigan

  • Washington University — Saint Louis

New York

  • Memorial Sloan Kettering Cancer Center — New York

Tennessee

  • SCRI Oncology Partners — Nashville

Texas

  • MD Anderson Cancer Center — Houston

Victoria

  • Peter MacCallum Cancer Centre — Melbourne

Ontario

  • Princess Margaret Hospital — Toronto

Trial Details

FieldValue
Enrollment Target 123 participants
Start Date 2018-06-06
Est. Completion 2026-11-30
Phase Phase 1

Sponsor

Genentech

206 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03448042

The ClinicalTrials.gov registry entry for NCT03448042 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 123 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Genentech, which has 206 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Solid Tumors appearing as the primary indexed condition, and to 3 interventions — of which Trastuzumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03448042 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Other, Connecticut, Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03448042 about?

NCT03448042 is a clinical study titled "A Study of Runimotamab in Participants With Locally Advanced or Metastatic HER2-Expressing Cancers". This study will evaluate the safety, tolerability, and pharmacokinetics of Runimotamab administered intravenously as a single agent and in combination with Trastuzumab in participants with locally advanced or metastatic Human Epidermal Growth Factor Receptor 2 (HER2)-expressing cancers.

What is the current status of trial NCT03448042?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 123 participants. The study started on 2018-06-06. Estimated completion is 2026-11-30.

What conditions does trial NCT03448042 study?

This clinical trial studies the following conditions: Solid Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03448042?

The interventions under investigation include: Trastuzumab (DRUG), Tocilizumab (DRUG), Runimotamab (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03448042?

This trial is sponsored by Genentech, which has 206 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03448042 being conducted?

This trial has 20 study locations across Connecticut, Michigan, New York, Tennessee, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial